Настройки

Укажите год
-

Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

Подробнее
-

Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

Подробнее

Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
Ведите корректный номера.
Ведите корректный номера.
Ведите корректный номера.
Ведите корректный номера.
Укажите год
Укажите год

Применить Всего найдено 3563. Отображено 198.
27-09-2001 дата публикации

ТЕРАПЕВТИЧЕСКИЙ АГЕНТ ДЛЯ ЛЕЧЕНИЯ ДИАБЕТА

Номер: RU2174114C2

Изобретение относится к новому терапевтическому лекарству для лечения диабета и включает соединение формулы I: R1-С(O)-C(R2 ')(R2)-Х-С(O)-R3, где Х представляет группу формулы -С(R4)(R5)-, -N(R6)-, -О-; где R4 - атом водорода, С1-С5 алкил, карбокси, фенил, C2-C5ацил, C2-C5алкоксикарбонил, R5 - атом водорода, C1-C5алкил; R6 - водород; R1 - фенил, необязательно замещен C1-C5алкилом, гидрокси, гидроксиалкилом, C2-C6алкенилом, ацилом, карбокси, тиенилом, C3-C7 циклоалкилом; бифенил, необязательно замещенный C1-C5алкилом или гидрокси; нафтил; терфенил; C3-C7циклоалкил, необязательно замещенный C1-C5алкилом или фенилом; необязательно замещенный C1-C5алкил; пиридил; бензотиенил; адамантил; инданил; флуоренил или группа ; R2 - водород, C1-C5алкил, необязательно замещенный карбокси; R2' - водород; R3 - C1 -C5алкил, необязательно замещенный фенилом или C1-C4алкокси; C1-C4алкокси; гидрокси; фенил; C3-C7циклоалкил, необязательно замещенный C1-C5алкилом; R2 и R7, взятые вместе, образуют группу -(CH2 ...

Подробнее
20-02-2006 дата публикации

ПРОИЗВОДНЫЕ 2-ИМИНОПИРРОЛИДИНА

Номер: RU2270192C2
Принадлежит: ЭЙСАЙ КО., ЛТД. (JP)

Предложены производные 2-иминопирролидина общей формулы (I), их соли и фармацевтические композиции, обладающие антагонистическим действием на рецепторы тромбина. Заместители A, R101, R102, R103, R5, R6, Y1, Y2, кольцо В, Ar определены в формуле изобретения. Технический результат: новые производные 2-иминопирролидина проявляют превосходные эффекты в отношении терапии или предупреждения заболеваний, связанных с тромбином. 9 н. и 28 з.п. ф-лы, 3 ил., 4 табл.

Подробнее
27-09-2015 дата публикации

ПРОМЕЖУТОЧНЫЕ ПРОДУКТЫ ДЛЯ ПОЛУЧЕНИЯ ИНГИБИТОРОВ НЕЙТРАЛЬНОЙ ЭНДОПЕПТИДАЗЫ И СПОСОБ ИХ ПОЛУЧЕНИЯ

Номер: RU2564024C2
Принадлежит: НОВАРТИС АГ (CH)

FIELD: chemistry. SUBSTANCE: invention relates to a novel method of producing intermediate products used to produce NEP inhibitors, particularly NEP inhibitors containing as the backbone chain γ-amino-δ-biphenyl-α-methylalkanoic acid or an ether of said acid, such as ethyl ether of N-(3-carboxy-1-oxopropyl)-(4S)-(p-phenylphenylmethyl)-4-amino-(2R)-methylbutanoic acid or a salt thereof. EFFECT: novel method of producing intermediate products used to produce NEP inhibitors. 15 cl, 35 ex РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 564 024 C2 (51) МПК C07D 207/277 (2006.01) C07D 207/263 (2006.01) C07D 207/267 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ (21)(22) Заявка: ИЗОБРЕТЕНИЯ К ПАТЕНТУ 2012135772/04, 21.01.2011 (24) Дата начала отсчета срока действия патента: 21.01.2011 Приоритет(ы): (30) Конвенционный приоритет: (72) Автор(ы): Дейвид ХУК (CH), Цзянгуан ЧЖОУ (CN), Юньчжон ЛИ (CN), Цзи КУ (CN) (43) Дата публикации заявки: 27.02.2014 Бюл. № 6 R U (73) Патентообладатель(и): НОВАРТИС АГ (CH) 22.01.2010 CN PCT/CN2010/070322 (45) Опубликовано: 27.09.2015 Бюл. № 27 (85) Дата начала рассмотрения заявки PCT на национальной фазе: 22.08.2012 (86) Заявка PCT: 2 5 6 4 0 2 4 (56) Список документов, цитированных в отчете о поиске: RU 2530900 C2, 20.10.2014 . WO 2009090251 A2, 23.07.2009 . US 5217996 A1, 08.06.1993 . EP 916656 B1, 10.09.2003 2 5 6 4 0 2 4 R U (87) Публикация заявки PCT: WO 2011/088797 (28.07.2011) Адрес для переписки: 129090, Москва, ул. Большая Спасская, 25, стр. 3, ООО "Юридическая фирма "Городисский и Партнеры" (54) ПРОМЕЖУТОЧНЫЕ ПРОДУКТЫ ДЛЯ ПОЛУЧЕНИЯ ИНГИБИТОРОВ НЕЙТРАЛЬНОЙ ЭНДОПЕПТИДАЗЫ И СПОСОБ ИХ ПОЛУЧЕНИЯ (57) Реферат: Изобретение относится к новому способу метилалкановую кислоту или эфир этой кислоты, получения промежуточных продуктов, такой как этиловый эфир N-(3-карбокси-1применимых для получения ингибиторов NEP, в оксопропил)-(4S)-(п-фенилфенилметил)-4-аминочастности ингибиторов NEP, содержащих в (2R)-метилбутановой ...

Подробнее
20-04-2000 дата публикации

СПОСОБ ПОЛУЧЕНИЯ АДАМАНТ-1-ИЛАМИНА И ЕГО ПРОИЗВОДНЫХ

Номер: RU2147573C1

Изобретение относится к химии производных адамантана, а именно к новому способу получения аминопроизводных адамантана общей формулы AdR, где R=NH2, NHBu-t, которые являются биологически активными веществами и могут найти применение в фармакологии, а адамант-1-иламин является основой лекарственного препарата "мидантан". Техническим результатом является повышение выхода заявляемых соединений, упрощение процесса получения и выделения конечных продуктов. Поставленный технический результат достигается в новом способе получения адамант-1-иламина и его производных указанной выше формулы взаимодействием производного адамантана с соответствующими аминами или их производными, причем в качестве производного адамантана используется 1,3-дегидроадамантан, а в качестве аминов или их производных - аммиак, трет.-бутиламин, формамид, морфолин, пиперидин, пирролидон-2, сукцинимид и фталимид; процесс проводят при мольном соотношении реагентов, равном 1:2 - 10, в присутствии каталитических количеств эфирата ...

Подробнее
10-03-2000 дата публикации

СПОСОБ ВЫДЕЛЕНИЯ АЦЕТИЛЕНА ИЗ СБРОСНЫХ ГАЗОВ

Номер: RU2146238C1

Изобретение относится к химической технологии, точнее, к усовершенствованному способу выделения ацетилена из сбросных газов процесса получения 1,4-бутиндиола (1,4-БИД) на базе ацетилена и формальдегида. Описывается способ выделения ацетилена из сбросных газов производства 1,4-бутиндиола из ацетилена и формальдегида и производства N-винилпирролидона винилированием α-пирролидона, содержащих ацетилен, азот, метанол и формальдегид, при этом осуществляют абсорбцию при избыточном давлении 0,02-1,0 МПа с использованием в качестве абсорбента смешанного растворителя, содержащего N-метилпирролидон и 1,4-бутандиол при концентрации последнего в абсорбенте 1-8 мас.% при объемном соотношении сбросный газ:абсорбент, равном (5-30):1, с последующей десорбцией ацетилена из насыщенного абсорбента при повышенной температуре и избыточном давлении 0,005-0,02 МПа. Технический результат - возможность утилизации ацетилена из сбросного газа, повышение качества и выхода целевого продукта.

Подробнее
11-03-2021 дата публикации

Дифармакофорные соединения ноотропно-анальгетического действия и способ их получения

Номер: RU2744571C1

Изобретение относится к дифармакофорным соединениям ноотропно–анальгетического действия формулы (1), где R-радикалы кислотных НПВС, таких как ибупрофен, диклофенак, индометацин, нифлумовая кислота, мефенамовая кислота, кетопрофен, декскетопрофен, напроксен, дифлунисал, кеторолак, сулиндак, фенопрофен, флурбипрофен, толметин, этодолак, флуфенамовая кислота, меклофенамовая кислота, толфенамовая кислота, дексиндопрофен. Технический результат: получены новые дифармакофорные соединения, которые проявляют одновременно анальгизирующее и ноотропное действие, что позволяет использовать предложенные соединения с обезболивающим эффектом одновременно для усиления когнитивных действий человека в условиях осложненной деятельности человека. 22 пр., 11 ил.(1) ...

Подробнее
10-05-2005 дата публикации

ПРОИЗВОДНЫЕ 2-ИМИНОПИРРОДИНА

Номер: RU2003133664A
Принадлежит:

... 1. Соединение, представленное формулой {где кольцо В представляет необязательно замещенное (1) ароматическое углеводородное кольцо или (2) ароматический гетероцикл, необязательно имеющий 1 или 2 атома азота; R101, R102 и R103 являются одинаковыми или различными и каждый представляет (1) водород или (2) группу, выбранную из группы заместителей С, представленной ниже; R5 представляет (1) водород, (2) циано, (3) галоген или (4) группу, выбранную из группы заместителей А, приведенной ниже; R6 представляет (1) водород, (2) С1-6алкил, (3) ацил, (4) карбамоил, (5) гидроксил, (6) С1-6алкокси, (7) С1-6 алкилоксикарбонилокси, (8) С3-8циклоалкил, (9) С1-6алкилоксикарбонил, необязательно замещенный ацилоксигруппой, или (10) С6-14ароматическую углеводородную кольцевую группу или 5-14-членную ароматическую гетероциклическую группу (причем каждый из предыдущих членов является необязательно замещенным по меньшей мере одной группой, выбранной из группы заместителей Е); Y1 представляет простую связь, -(CH2 ...

Подробнее
23-04-1990 дата публикации

Способ получения N-метилпирролидона

Номер: SU1558903A1
Принадлежит:

Изобретение касается гетероциклических веществ, в частности получения N-метил-пирролидона - полупродукта для синтеза полезных веществ, растворителя мономеров и полимеров. Цель - повышение активности катализатора. Синтез N-метилпирролидона ведут конденсацией избытка металламина с γ-бутиролактоном при 250св присутствии катализатора - аморфного алюмосиликата, содержащего 5-30 мас.% оксида алюминия. Для упрощения процесса его ведут при давлении 5 атм (для перевода монометиламина в жидкую фазу). Эти условия повышают длительность работы катализатора до 5 ч при получении 99%-ного выхода N-метилпирролидона, в то время, как в известном способе выход снижается на 20% через 4 ч работы на цеолите типа У. 1 з.п. ф-лы, 1 табл.

Подробнее
12-01-1976 дата публикации

Номер: DD0000117450A5
Автор:
Принадлежит:

Подробнее
28-07-1988 дата публикации

Process for the preparation of pyrrolidone or N-methylpyrrolidone

Номер: DE0003701297A1
Принадлежит:

Process for the preparation of pyrrolidone or N-methylpyrrolidone by reacting methylamines with acrylonitrile in the presence of a peroxide free-radical initiator at temperatures from 150 to 220@C.

Подробнее
13-11-2003 дата публикации

Verfahren zur Herstellung von Aziridinen und N-Vinylamiden

Номер: DE0010318326A1
Принадлежит:

Bei der Herstellung von Aziridinen oder N-Vinylamiden, jeweils aus Alkanolaminen oder Alkanolamiden, anhand eines bekannten Verfahrens, welches einen Reaktionsschritt, einen Sammelschritt und/oder einen Kondensationsschritt, einen Reinigungsschritt und einen Wiedererlangungsschritt aufweist, ist diese Erfindung auf das Verhindern der Bildung von einer festen Substanz in den Vakuumpumpen und den Vakuumlinien gerichtet. Gegenstand dieser Erfindung ist erfüllt durch das Ausführen der Dekompression bei dem Reinigungsschritt und der Dekompression bei dem Wiedererlangungsschritt in beiderseitig verschiedenen Dekompressionssystemen.

Подробнее
10-04-2008 дата публикации

VERFAHREN ZUR REINIGUNG VON N-VINYLPYRROLIDON

Номер: DE602004007657T2

Подробнее
02-03-1978 дата публикации

Номер: DE0002325139C3
Принадлежит: TEIJIN LTD., OSAKA (JAPAN)

Подробнее
28-08-1975 дата публикации

1-AMINOMETHYLACE-NAPHTHENES AND THEIR PRODUCTION

Номер: GB0001404021A
Автор:
Принадлежит:

Подробнее
29-05-1975 дата публикации

PROCESS FOR THE DIMERIZATION OF VINYL PYRROLODONE

Номер: GB0001395964A
Автор:
Принадлежит:

... 1395964 Dimerization of N-vinyl pyrrolidone GAF CORP 9 Aug 1972 [16 Aug 1971] 37161/72 Heading C2C 1,3 - Bis - (2 - pyrrolidonyl) - 1 - butene is obtained by dimerizing N-vinyl-pyrrolidone with an acid catalyst at 65‹ to 150‹ C. Sufficient acid catalyst (e.g. CF 3 CO 2 H), is preferably added to initiate an exothermic reaction, e.g. from 0À01 to 20% by weight based on N-vinyl pyrrolidone. An inert atmosphere for the reaction is preferred and an inert organic solvent is optional. Other exemplified acid catalysts are H 2 SO 4 , CH 2 CO 2 H, HCl, HI and HF and acids otherwise specified are phosphoric, nitric, BF 3 , SO 2 and polystyrene sulphonic acid.

Подробнее
04-02-1976 дата публикации

PRODUCTION OF POLYAMIDE FIBRES

Номер: GB0001423441A
Автор:
Принадлежит:

... 1423441 Aromatic polyamide filaments TEIJIN Ltd 17 May 1973 [18 May 1972 13 June 1972] 23693/73 Heading B5B Wholly aromatic polyamide fibres are made by extruding a spinning solution of a wholly aromatic polyamide in an amide solvent into an aqueous coagulating bath containing an inorganic salt, the process comprising feeding an aqueous coagulating liquid containing calcium chloride and having an amide solvent concentration of not more than 3% by weight to the vicinity of a spinneret, flowing the coagulating liquid at an average velocity not more than 0À1 times that of the take-up of the yarn, (preferably from 0À04 to 0À1 times), discharging the coagulating liquid having an amide solvent concentration of not less than 4% by weight from said bath, treating the coagulating liquid with an organic solvent consisting substantially of methylene chloride, and extracting and recovering the amide solvent from the coagulating liquid. Suitable solvents for the polyamides, which should contain at least ...

Подробнее
24-03-1965 дата публикации

Bacteriostatic adducts of dichloroanilides

Номер: GB0000987251A
Автор: MCKAY ARTHUR FERGUSON
Принадлежит:

The invention comprises bacteriostatic adducts of 3,4-dichloroanilides of formula where Q is a chlorinated aryl radical of formula with an adduct forming compound which is 2-hydroxy- or 2 - amino - 4,6 - dimethylpyrimidine, or 2 - amino - 4,6 - dimethylpyrimidine, N,N1-diacetylpiperazine or its 2-methyl or trans-2,5-dimethyl derivatives, N-acetylpiperidine or its 2-methyl derivative, N,N-diisopropyl or diphenyl acetamide, 1-methyl- or 1,5-dimethyl - 2 - phenylpyrazolone - 3,3 - amino - 5,6-dimethyl-as-triazine, N-methyl-2-pyrrolidone, N - methyl - 2 - pyridone or N - methyl - e - caprolactam. The adducts are probably hydrogen-bonded. They are made by mixing the components, conveniently in a common solvent, the adduct may crystallize out or be precipitated by addition of a non-solvent. Heat may be used.ALSO:The growth of bacteria on a surface is controlled by the application of bacteriostatic adducts of 3,4-dichloroanilides of formula Подробнее

16-08-1967 дата публикации

Process for preparing n-vinyl compounds

Номер: GB0001079314A
Автор:
Принадлежит:

N-vinyl compounds of the formula wherein R1 and R2 is each an alkyl group, or in which R1 and R2 are linked with each other as a ring so as to form an alkylene group which may be substituted by an alkyl group, and in which R3 and R4 is hydrogen or an alkyl group, are obtained by catalytically splitting a compound of the formula wherein R5 is an alkyl group by heating the latter in the liquid phase in the presence of a catalyst comprising an acid activated aluminium oxide, an aluminium phosphate, a zirconium dioxide or a mixture of more than one of these substances. The reaction is suitably effected under reduced pressure at 50-180 DEG C. employing an amount of catalyst within the range 0.5 to 15 mols per cent. The reaction may be effected under an atmosphere of nitrogen and a stabilizer, e.g. hydroquinone, may be present.

Подробнее
15-12-1979 дата публикации

Method of preparation of 1-alkylène-2-aminométhylpyrrolidines.

Номер: OA0000004150A
Автор:
Принадлежит:

Подробнее
30-06-2004 дата публикации

N,N' -substituted-1,3-diamino -2-hydroxypropane derivatives.

Номер: AP2004003049A0
Принадлежит:

Disclosed are compounds of the formula (0, wherein the variables RN, RC, R1, R25, R2, and R3 are as defined herein. These compounds have activity as inhibitors of betasec-retase and are therefore useful in treating a variety of discorders such as Alzheimer's Disease.

Подробнее
15-01-1966 дата публикации

Composed weedkillers containing lactams.

Номер: OA0000000113A
Автор:
Принадлежит:

Подробнее
31-10-1980 дата публикации

New method of preparation of the 2-aminométhyl pyrrolidine.

Номер: OA0000004856A
Автор:
Принадлежит:

Подробнее
28-02-1981 дата публикации

News N-alkanol substituted amines hétérocyclines their derivatives, their methods of preparation.

Номер: OA0000005344A
Автор:
Принадлежит:

Подробнее
15-04-2010 дата публикации

PROCEDURE FOR THE PRODUCTION OF LACTAMS

Номер: AT0000462690T
Принадлежит:

Подробнее
15-06-1976 дата публикации

JODOPHOR-ZUSAMMENSETZUNG UND VERFAHREN ZU IHRER HERSTELLUNG

Номер: ATA393774A
Автор:
Принадлежит:

Подробнее
15-09-1978 дата публикации

Process for the depletion of 7-amino-3-((E)-1-propen- 1-yl)-3-cephem-4-carboxylic acid

Номер: ATA399876A
Автор:
Принадлежит:

Подробнее
15-07-1996 дата публикации

ARYL-SUBSTITUTED RHODANINDERIVATE

Номер: AT0000139531T
Принадлежит:

Подробнее
15-08-1989 дата публикации

PROCEDURE FOR THE PRODUCTION OF GAMMABUTYROLACTAMEN.

Номер: AT0000044733T
Принадлежит:

Подробнее
26-03-1973 дата публикации

Procedure for the production of new Pyrrolidin-2-onderivate and their salts

Номер: AT0000305997B
Автор:
Принадлежит:

Подробнее
15-08-2003 дата публикации

PROCEDURE FOR THE PRODUCTION OF N-METHYL-PYRROLIDON

Номер: AT0000246173T
Принадлежит:

Подробнее
25-10-1971 дата публикации

Procedure for the production of new Cephalosporinderivate

Номер: AT0000293614B
Автор:
Принадлежит:

Подробнее
28-02-2019 дата публикации

Compositions for the treatment of pulmonary fibrosis

Номер: AU2017301113A1
Принадлежит: Shelston IP Pty Ltd.

The present invention relates to compounds and their use in the prophylactic and/or therapeutic treatment of pulmonary fibrosis and/or related conditions.

Подробнее
29-10-1987 дата публикации

- ALLENYL- - AMINOBUTYRIC ACIDS

Номер: AU0000566709B2
Принадлежит:

Подробнее
30-04-2015 дата публикации

Anti-fibrotic pyridinones

Номер: AU2013327505A1
Принадлежит:

Disclosed are pyridinone compounds, method for preparing these compounds, and methods for treating fibrotic disorders.

Подробнее
11-04-2002 дата публикации

A process for the production of N-methyl pyrrolidone

Номер: AU0000746000B2
Принадлежит:

Подробнее
28-10-1982 дата публикации

PYRROLIDINE DERIVATIVES

Номер: AU0000525204B2
Принадлежит:

Подробнее
14-10-1982 дата публикации

HETEROCYCLIC-SUBSTITUTED ANILIDE DERIVATIVES

Номер: AU0000525011B2
Принадлежит:

Подробнее
04-01-1990 дата публикации

TRANSVINYLATION REACTION

Номер: AU0003717789A
Принадлежит: Union Carbide Corp

A process for the transvinylation of a vinyl derivative of a Bronsted acid with a different Bronsted acid which comprises providing a liquid phase mixture containing said vinyl derivative and said Bronsted acid in the presence of a ruthenium compound at a temperature at which transvinylation occurs and recovering as a product of transvinylation the vinyl derivative of the different Bronsted acid. The process is most favorably employed using carboxylic acids to make vinyl esters of carboxylic acids.

Подробнее
10-11-1981 дата публикации

CONTINUOUS POLYMERIZATION OF 2-PYRROLIDONE

Номер: CA0001112396A1
Принадлежит:

Подробнее
17-07-2008 дата публикации

PROCESS FOR PREPARING 5-BIPHENYL-4-AMINO-2-METHYL PENTANOIC ACID

Номер: CA0002674291A1
Принадлежит:

The present invention relates to pyrrolidin-2-ones according to the formu la (1), or salts thereof, wherein R1 is hydrogen or a nitrogen protecting gr oup, methods for their preparation and their use in the preparation of NEP-i nhibitors, particularly in the preparation of N-(3-carboxyl-1-oxopropyl)-(4S )-(p-phenylphenylmethyl)-4-amino-(2R)-methyl butanoic acid ethyl ester or sa lt thereof.

Подробнее
14-01-2021 дата публикации

METHOD FOR PURIFYING WASTE N-METHYL-2-PYRROLIDONE MIXED SOLUTION

Номер: CA3137186A1
Принадлежит:

The present invention relates to a method for purifying a waste N-methyl-2-pyrrolidone (hereinafter referred to as NMP) mixture solution and, more specifically, to a method for purifying a waster NMP mixture solution by using a base. According to the present invention, by applying the base to the waste NMP mixture solution, NMS and GBL can be simultaneously removed to collect high-purity NMP.

Подробнее
10-11-1981 дата публикации

CONTINUOUS POLYMERIZATION OF 2-PYRROLIDONE

Номер: CA1112396A
Принадлежит: CHEVRON RES, CHEVRON RESEARCH COMPANY

... 2-Pyrrolidone is continuously polymerized to a high-molecular-weight particulate product by the stirred polymerization of the carbonated alkaline polymerizate. The polymerizate is prepared by contacting an aqueous hydroxide with excess 2-pyrrolidone, maintaining the resultant alkaline mixture at an elevated temperature for sufficient time to reduce the 2pyrrolidone dimer content of the mixture to within the desired limits, dehydrating the alkaline mixture to reduce the water content to within the desired limits, and contacting the alkaline mixture with carbon dioxide to form the carbonated alkaline polymerizate. The paste of particulate polypyrrolidone and liquid polymerizate is continuously withdrawn from the reactor, neutralized with aqueous acid and washed with warm water.

Подробнее
19-05-1981 дата публикации

PROCESS FOR PREPARING 2-PYRROLIDONE

Номер: CA1101429A
Принадлежит: STAMICARBON, STAMICARBON B.V.

PROCESS FOR PREPARING 2-PYRROLIDONE An improved process for the preparation of 2-pyrrolidone by the liquid phase hydrogenation of succinonitrile in the presence of a hydrogenation catalyst and ammonia, whereafter the resulting hydrogenation product is hydrolyzed with water. A hydrogenation catalyst in the form of a fixed bed is used, and a liquid phase of succinonitrile and liquid ammonia is passed over the catalyst at a temperature of between 50 and 130.degree.C.

Подробнее
19-02-1991 дата публикации

PROCESS FOR THE PREPARATION OF CLAUSENAMIDE

Номер: CA0001280427C

A new synthetic route to clausenamide having the formula has been found. It has been found that a compound of the formula can be oxidized to provide the stereochemically correctly configured product, clausenamide. A number of new compounds useful in the total synthesis of clausenamide have also been found. These compounds have the general formula wherein R is ?-C6H5, CHO, ?-C6H5 and CH20. Clausenamide shows an antiamnesic action and an action affording protection from cerebral hypoxia in animal experiments.

Подробнее
07-10-2004 дата публикации

PRODUCTION OF N-(METHYL-ARYL)-2-LACTAM,N-(METHYL CYCLOAKLYL)-2-LACTAM AND N-ALKYL-2-LACTAM BY REDUCTIVE AMINATION OF LACTONES WITH ARYL AND ALKYCYANO COMPOUNDS

Номер: CA0002520448A1
Автор: MANZER, LEO ERNEST
Принадлежит:

This invention relates to a process for producing N-(methyl aryl)-2-lactams, N- alkyl-2-lactams, and N-(methyl cycloalkyl)-2-lactams by reductive amination of lactones with aryl or alkyl cyano compounds utilizing a metal catalyst, which is optionally supported.

Подробнее
07-10-2004 дата публикации

PRODUCTION OF 5-METHYL-N-ARYL-2-PYRROLIDONE AND 5-METHYL-N-CYCLOALKYL-2-PYRROLIDONE BY REDUCTIVE AMINATION OF LEVULINIC ACID WITH ARYL AMINES

Номер: CA0002520425A1
Автор: MANZER, LEO ERNEST
Принадлежит:

This invention relates to a process for producing 5-methyl-N-aryl-2- pyrrolidone and 5-methyl-N-cycloalkyl-2-pyrrolidone by reductive amination of levulinic acid or its derivatives with aryl amines, ammonia or ammonium hydroxide utilizing a metal catalyst, which is optionally supported.

Подробнее
07-10-2004 дата публикации

PRODUCTION OF 5-METHYL-1-HYDROCARBYL-2-PYRROLIDONE BY REDUCTIVE AMINATION OF LEVULINIC ACID

Номер: CA0002520242A1
Принадлежит:

This invention relates to a process for producing 5-methyl-1-R-2-pyrrolidone or 5-methyl-2-pyrrolidone, wherein R is a hydrocarbyl or substituted hydrocarbyl, by reductive amination of levulinic acid utilizing a metal catalyst, which may be optionally supported.

Подробнее
07-10-2004 дата публикации

PRODUCTION OF 5-METHYL-N-(METHYL ARYL)-2-PYRROLIDONE, 5-METHYL-N-(METHYL CYCLOALKYL)-2-PYRROLIDONE AND 5-METHYL-N-ALKYL-2-PYRROLIDONE BY REDUCTIVE AMINATION OF LEVULINIC ACID ESTERS WITH CYANO COMPOUNDS

Номер: CA0002520428A1
Автор: MANZER, LEO ERNEST
Принадлежит:

This invention relates to a process for producing 5-methyl-1-R-2-pyrrolidone or 5-methyl-2-pyrrolidone, wherein R is a hydrocarbyl or substituted hydrocarbyl, by reductive amination of levulinic acid utilizing a metal catalyst, which may be optionally supported.

Подробнее
08-09-1981 дата публикации

PRODUCTION OF PYRROLIDIN-2-ONES FROM 2-PYRROLIN-2- ONES AND THE PRODUCTION OF 3-PYRROLIN-2-ONES

Номер: CA0001108628A1
Автор: HOFER PETER
Принадлежит:

Подробнее
01-10-1974 дата публикации

PREPARATION OF 2-PYRROLIDINONE

Номер: CA0000955598A1
Автор: DAVIS RONALD I
Принадлежит:

Подробнее
02-08-1983 дата публикации

CATALYST AND PROCESS FOR THE PRODUCTION OF PYRROLIDONE

Номер: CA0001151138A1
Принадлежит:

Подробнее
22-09-2016 дата публикации

COMPOSITIONS FOR THE TREATMENT OF FIBROSIS AND FIBROSIS-RELATED CONDITIONS

Номер: CA0002979413A1
Принадлежит: BERESKIN & PARR LLP/S.E.N.C.R.L.,S.R.L.

The present invention relates to novel compounds and their use in the prophylactic and/or therapeutic treatment of fibrosis and fibrosis-related conditions.

Подробнее
10-04-2014 дата публикации

ANTI-FIBROTIC PYRIDINONES

Номер: CA0002884251A1
Принадлежит:

Disclosed are pyridinone compounds, method for preparing these compounds, and methods for treating fibrotic disorders.

Подробнее
21-01-1994 дата публикации

AMINEDIOL PROTEASE INHIBITORS

Номер: CA0002100894A1
Принадлежит:

AMINEDIOL PROTEASE INHIBITORS Novel aminediol compounds, pharmaceutical compositions containing these compounds, and methods of using these compounds in inhibiting retroviral protease, particularly useful in the treatment and/or prevention of HIV infection (AIDS).

Подробнее
08-01-1998 дата публикации

NICKEL CATALYZED ADDITION OF -NH- CONTAINING COMPOUNDS TO VINYL AND ARYL HALIDES

Номер: CA0002258594A1
Принадлежит:

A process for producing unsaturated nitrogen containing compounds such as enamides, enamines and aryl amines/amides is disclosed. A vinyl halide or aryl halide is reacted with an -NH- containing compound in the presence of a catalytic amount of a catalyst precursor composition comprising a zero-valent nickel and an organophosphine or carbene ligand. One step coupling of vinyl halides and aryl halides with -NH- containing compounds is made possible by practice of the invention.

Подробнее
15-06-1976 дата публикации

Номер: CH0000576442A5
Автор:

Подробнее
13-12-1974 дата публикации

VERFAHREN ZUR HERSTELLUNG VON 1-ALKENYL-2-AMINOMETHYLPYRROLIDINEN.

Номер: CH0000556836A
Автор:
Принадлежит: FRATMANN AG

Подробнее
15-03-1976 дата публикации

Номер: CH0000573404A5
Автор:

Подробнее
15-01-1976 дата публикации

Номер: CH0000571489A5
Автор:

Подробнее
15-05-1972 дата публикации

Procédé de préparation de nouveaux dérivés de la pyrrolidine

Номер: CH0000522635A
Принадлежит: ROUSSEL UCLAF, ROUSSEL-UCLAF

Подробнее
31-08-1982 дата публикации

PROCEDURE FOR THE PRODUCTION OF OLEFINI DERIVATIVES OF AMINO ACIDS.

Номер: CH0000631696A5
Принадлежит: MERRELL TORAUDE & CO, MERRELL TORAUDE ET CIE

Подробнее
30-06-1982 дата публикации

PROCEDURE FOR THE PRODUCTION OF NEW ACETYLENE DERIVATIVES OF AMINO ACIDS.

Номер: CH0000630604A5
Принадлежит: MERRELL TORAUDE & CO, MERRELL TORAUDE ET CIE

Подробнее
28-12-1979 дата публикации

Process for the preparation of substituted heterocyclic N-alkanolamines

Номер: CH0000614939A5

Compounds of formula IV which have good pharmacological properties are prepared by reaction of a lower alkyl sulphate, an alkali metal alkoxide and a lower nitroalkane with a compound of formula I and subsequent reduction of the intermediate compound. By an oxidation of the compounds of formula IV, N-oxide compounds are obtained. The compounds obtained are intermediates in the synthesis of heterocyclic benzamides, such as those which are described in Swiss Patent No. 596,175, used as antiemetic agents.

Подробнее
28-12-1979 дата публикации

Номер: CH0000614858A5

Подробнее
14-03-2013 дата публикации

MODULATION OF BIOACTIVE EPOXY-FATTY ACID LEVELS BY PHOSPHODIESTERASE INHIBITORS

Номер: US20130065936A1

The present invention provides method for increasing levels of epoxygenated fatty acids by administration of a phosphodiesterase inhibitor. 1. A method of increasing levels of epoxygenated fatty acids in a subject in need thereof comprising administering to the subject an inhibitor of a phosphodiesterase.2. The method of claim 1 , wherein the ratio of epoxygenated fatty acids to dihydroxy fatty acids is increased without changing the levels of dihydroxy fatty acids.3. The method of claim 1 , wherein soluble epoxide hydrolase is not inhibited.4. The method of claim 1 , wherein the inhibitor of phosphodiesterase is an inhibitor of PDE4.5. The method of claim 4 , wherein the inhibitor of PDE4 is selected from the group consisting of rolipram claim 4 , roflumilast claim 4 , cilomilast claim 4 , ariflo claim 4 , HT0712 claim 4 , ibudilast claim 4 , mesembrine claim 4 , pentoxifylline claim 4 , piclamilast claim 4 , and combinations thereof.6. The method of claim 1 , wherein the inhibitor of phosphodiesterase is an inhibitor of PDE5.7. The method of claim 1 , wherein the inhibitor of phosphodiesterase is administered in a subtherapeutic dose.8. The method of claim 1 , further comprising administration of an inhibitor of soluble epoxide hydrolase.9. The method of claim 8 , wherein the inhibitor of soluble epoxide hydrolase is administered in a subtherapeutic dose.10. The method of claim 1 , wherein the epoxygenated fatty acids are cis-epoxyeicosantrienoic acids (“EETs”) claim 1 , epoxides of linoleic acid claim 1 , epoxides of eicosapentaenoic acid (“EPA”) or epoxides of docosahexaenoic acid (“DHA”) claim 1 , or a mixture thereof.11. A method of obtaining analgesic claim 1 , anti-convulsant claim 1 , anti-depressant claim 1 , anti-inflammatory claim 1 , anti-hypertensive claim 1 , cardioprotective claim 1 , organ protective effects in a subject in need thereof claim 1 , comprising administering to the subject an inhibitor of phosphodiesterase.12. A method of reducing claim ...

Подробнее
06-06-2013 дата публикации

PROCESSES FOR THE PRODUCTION OF PYRROLIDONES

Номер: US20130144070A1
Принадлежит: BIOAMBER S.A.S.

Processes for making pyrrolidones include making MAS and/or SA from a clarified DAS- and/or MAS-containing fermentation broth and converting the MAS or SA to the pyrrolidones, typically with catalysts at selected temperatures and pressures. 7. The processes of claim 1 , wherein the distillations arc carried out in the presence of an ammonia separating solvent which is at least one selected from the group consisting of diglyme claim 1 , triglyme claim 1 , tetraglyme claim 1 , sulfoxides claim 1 , amides claim 1 , sulfones claim 1 , polyethyleneglycol (PEG) claim 1 , butoxytriglycol claim 1 , N-methylpyrolidone (NMP) claim 1 , ethers claim 1 , and methyl ethyl ketone (MEK) or in the presence of a water azeotroping solvent which is at least one selected from the group consisting of toluene claim 1 , xylene claim 1 , methylcyclohexane claim 1 , methyl isobutyl ketone claim 1 , hexane claim 1 , cyclohexane and heptane.14. The processes of claim 2 , wherein the distillations are carried out in the presence of an ammonia separating solvent which is at least one selected from the group consisting of diglyme claim 2 , triglyme claim 2 , tetraglyme claim 2 , sulfoxides claim 2 , amides claim 2 , sulfones claim 2 , polyethyleneglycol (PEG) claim 2 , butoxytriglycol claim 2 , N-methylpyrolidone (NMP) claim 2 , ethers claim 2 , and methyl ethyl ketone (MEK) or in the presence of a water azeotroping solvent which is at least one selected from the group consisting of toluene claim 2 , xylene claim 2 , methylcyclohexane claim 2 , methyl isobutyl ketone claim 2 , hexane claim 2 , cyclohexane and heptane claim 2 ,15. The processes of claim 3 , wherein the distillations are carried out in the presence of an ammonia separating solvent which is at least one selected from the group consisting of diglyme claim 3 , triglyme claim 3 , tetraglyme claim 3 , sulfoxides claim 3 , amides claim 3 , sulfones claim 3 , polyethyleneglycol (PEG) claim 3 , butoxytriglycol claim 3 , N-methylpyrolidone ...

Подробнее
11-07-2013 дата публикации

Processes for the production of pyrrolidones

Номер: US20130178637A1
Принадлежит: Bioamber SAS

Processes for making pyrrolidones include providing a clarified diammonium succinate (DAS)-containing and/or monoammonium succinate (MAS)-containing fermentation broth; distilling the broth under super atmospheric pressure at a temperature of greater than 100° C. to about 300° C. to form an overhead that includes water and ammonia, and a liquid bottoms that includes SA, and at least about 20 wt % water; cooling and/or evaporating the bottoms to attain a temperature and composition sufficient to cause the bottoms to separate into a liquid portion and a solid portion that is substantially pure SA; separating the solid portion from the liquid portion; and converting the solid SA portion to pyrrolidones.

Подробнее
07-11-2013 дата публикации

HIGH STABLE NON-IONIC N-VINYL BUTYROLACTAM IODINE AND PREPARATION METHOD THEREOF

Номер: US20130296576A1
Автор: Chen Zhan, Wang Yu

The present invention relates to a preparation method of a high-stable non-ionic N-vinyl butyrolactam iodine, wherein non-ionic N-vinyl butyrolactam, iodine and at least one grinding aid are stirred at 150-800 r/min at a temperature of 50° C.-90° C. for 1 to 12 hours to prepare the high-stable non-ionic N-vinyl butyrolactam iodine, wherein the K value of the non-ionic N-vinyl butyrolactam is 32±1, the PD value of the main peak of the non-ionic N-vinyl butyrolactam is ≦1.6, the moisture content of the non-ionic N-vinyl butyrolactam is ≦2.5%, preferably, the grinding aid is selected one or several from sodium chloride, sodium citrate, sodium carbonate and sodium phosphate, the amount of the grinding aid added is 0.02 to 2% of the total amount of the non-ionic N-vinyl butyrolactam and the iodine, the non-ionic N-vinyl butyrolactam is PVP-K32, the high-stable non-ionic N-vinyl butyrolactam iodine prepared by the above mentioned method is also provided, the stability of the high-stable non-ionic N-vinyl butyrolactam iodine of the present invention is high, thereby facilitating long-term storage and use, thus the high-stable non-ionic N-vinyl butyrolactam iodine is suitable for large-scale popularization.

Подробнее
30-01-2014 дата публикации

Process and Intermediates for the Synthesis of 8-[-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one Compounds

Номер: US20140031549A1
Принадлежит: Opko Health Inc

This application discloses a novel process to synthesize 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds, which may be used, for example, as NK-1 inhibitor compounds in pharmaceutical preparations, intermediates useful in said process, and processes for preparing said intermediates; also disclosed is a process for removal of metals from N-heterocyclic carbine metal complexes.

Подробнее
01-01-2015 дата публикации

Method for cleaning deposits from equipment that have accumulated during a method for recovering nmp, by the introduction of hot water and agitation

Номер: US20150000706A1
Принадлежит: BASF SE

A process is proposed for cleaning an apparatus to remove deposits from a process for the recovery of purified N-methylpyrrolidone (NMP) by evaporating NMP from a contaminated NMP stream which is obtained in a process for the extractive separation of acetylene from the reaction mixture of a partial oxidation of hydrocarbons after expulsion of the acetylene as a gas, wherein hot water is passed into the apparatus and is stirred.

Подробнее
02-01-2020 дата публикации

PROCESS FOR PREPARING BRIVARACETAM

Номер: US20200002278A1
Автор: Ma Liang
Принадлежит: BEIJING ABLEPHARMTECH CO., LTD.

The present invention discloses a novel process for preparing Brivaracetam, belonging to the field of chemical synthesis. According to the process, optically pure (R)-4-n-propyl-dihydrofuran-2(3H)-one was used as a starting material, after the steps of ring opening, halogenation, condensation, ring-closing, etc, high-purity Brivaracetam is given. The preparation process has the advantages of easy availability of raw materials, low price, high yield, high optical purity of product, simple reaction conditions and simple operations. 2. The preparation process according to claim 1 , wherein the acid-binding agent is an organic base claim 1 , and the solvent for the condensation reaction is an aprotic solvent.3. The preparation process according to claim 2 , wherein the acid-binding agent is one or more from triethylamine claim 2 , pyridine claim 2 , N claim 2 ,N-diisopropylethylamine claim 2 , 1 claim 2 ,8-diazabicyclo[5.4.0]undec-7-ene claim 2 , 1 claim 2 ,4-diazabicyclo [2.2.2]octane claim 2 , N claim 2 ,N-dimethylaminopyridine claim 2 , N claim 2 ,N-dimethyl-p-toluidine claim 2 , and the solvents for the condensation reaction are any one or more from dichloromethane claim 2 , chloroform claim 2 , tetrahydrofuran claim 2 , methyltetrahydrofuran claim 2 , methyl tert-butyl ether claim 2 , isopropyl ether claim 2 , 1 claim 2 ,4-dioxane claim 2 , ethyl acetate claim 2 , isopropyl acetate claim 2 , tert-butyl acetate claim 2 , methyl acetate claim 2 , ethyl formate.4. The preparation process according to claim 3 , wherein the acid-binding agent is triethylamine or pyridine claim 3 , and the solvent for condensation reaction is tetrahydrofuran.5. The preparation process according to claim 1 , wherein the molar ratio of the compound of formula III to the acid-binding agent is 1:1-10 claim 1 , the molar ratio of the compound of formula III to (S)-2-aminobutanamide is 1:0.5-5 claim 1 , and the temperature of the condensation reaction is −10 to 50° C.6. The preparation process ...

Подробнее
01-01-2015 дата публикации

METHOD FOR CONVERSION OF DIAMMONIUM SUCCINATE IN FERMENTATION BROTH TO 2-PYRROLIDONE AND N-METHYLPYRROLIDONE

Номер: US20150005510A1
Принадлежит: Myriant Corporation

This invention relates to a process for preparing 2-pyrrolidone (also called 2-pyrrolidinone) and N-methylpyrrolidone (also called N-methylpyrrolidinone) from diammonium succinate in fermentation broth. In the first stage of this invention, renewable carbon resources are utilized to produce diammonium succinate through biological fermentation. In the second stage of this present invention, diammonium succinate is converted into 2-pyrrolidone and N-methylpyrrolidone through a two step reaction. Both the steps of the reaction leading to the production of 2-pyrrolidone and N-methylpyrrolidone are carried out in a solvent phase to prevent the loss of succinimide through hydrolysis. 1. A process for preparing succinimide comprising the steps of:(a) providing a fermentation broth comprising diammonium succinate;(b) adding a polar organic solvent with boiling point higher than that of water to said fermentation broth;(c) evaporating water in said fermentation broth;(d) raising temperature of said fermentation broth to at least 120° C. to convert said diammonium succinate to succinimide.2. The Process according to claim 1 , wherein said fermentation broth is a concentrated fermentation broth.3. The process according to claim 1 , wherein said fermentation broth is subjected to ultrafiltration process before converting diammonium succinate to succinimide.4. The process according to claim 1 , wherein said fermentation broth is subjected to adsorption process to remove sugars and amino acids in the fermentation broth.5. The process according to claim 1 , wherein said polar organic solvent is selected from a group consisting of diglyme claim 1 , triglyme claim 1 , tetraglyme claim 1 , propylene glycol claim 1 , dimethylsulfoxide claim 1 , dimethylformamide claim 1 , dimethylacetamide claim 1 , dimethylsulfone claim 1 , sulfolane claim 1 , polyethylene glycol claim 1 , butoxytriglycol claim 1 , N-methylpyrrolidone claim 1 , 2-pyrrolidone claim 1 , gammabutyrolactone claim 1 , ...

Подробнее
11-01-2018 дата публикации

DESALINATION OF POLYARYL ETHERS BY MEANS OF MELT EXTRACTION

Номер: US20180009944A1
Принадлежит:

A method for desalinating a salt-containing polymer (SP) comprising a polyaryl ether having a softening temperature Tand a salt (S), comprising the steps of 113.-. (canceled)14. A method for desalinating a salt-containing polymer (SP) comprising a polyaryl ether having a softening temperature Tand a salt (S) , comprising the steps of{'sub': 1', 'S, 'a) providing the salt-containing polymer (SP) at a first temperature Tabove the softening temperature Tof the polyaryl ether,'}b) contacting the salt-containing polymer (SP) provided in step a) with an extractant (E) to obtain a desalinated polymer (DP) comprising the polyaryl ether, and a salt-containing extractant (SE) comprising the extractant (E) and the salt (S),wherein step a) comprises the following steps:i) providing a first salt-containing polymer (SP1) comprising the polyaryl ether and the salt (S),ii) pelletizing the first salt-containing polymer (SP1) provided in step i) to obtain a pelletized first salt-containing polymer (PSP1),iii) contacting the pelletized first salt-containing polymer (PSP1) obtained in step ii) with the extractant (E) to obtain the salt-containing polymer (SP) comprising the polyaryl ether and residues of the salt (S), and a first salt-containing extractant (SE1) comprising the extractant (E) and a portion of the salt (S),{'sub': 1', 'S, 'iv) heating the salt-containing polymer (SP) obtained in step iii) to a first temperature Tabove the softening temperature Tof the polyaryl ether,'}and wherein step b) comprises the following step:v) contacting the salt-containing polymer (SP) heated in step iv) with the extractant (E) to obtain the desalinated polymer (DP) comprising the polyaryl ether, and a second salt-containing extractant (SE2) comprising the extractant (E) and the residues of the salt (S),wherein the first salt-containing polymer (SP1) is provided in step i) by a melt polymerization method.15. The method according to claim 14 , wherein the salt-containing polymer (SP) is ...

Подробнее
19-02-2015 дата публикации

PROCESS FOR PREPARING LACTAMS

Номер: US20150051401A1
Принадлежит:

The present invention relates to a method for preparing lactams using heterogeneous catalysis by hydrogenating at least one compound of the following formula (I), where A is a radical of the following formula (I′) or (II′): —CH(R)—CH(R)— (I′); or —CH(R)—CH(R)—CH(R)— (II′); where R, Rand Rare, independently from each other, H, OH, an alkyl radical, or a cycloalkyl radical; and R is H or a straight or branched alkyl radical having 1 to 20, preferably 1 to 10, and more preferably 1 to 4 carbon atoms. Said method is carried out at a pressure of less than 60 bars, preferably 10 to 50 bars, in the presence of a solid hydrogenation catalyst including at least two metals selected from the group of noble metals and transition metals, and an inert substance used as a support, wherein said compound of formula (I) can be used alone or as part of a mixture. 2. The process of claim 1 , wherein the hydrogenation is carried out in the absence of solvent.3. The process of claim 1 , wherein the hydrogenation is carried out in the liquid phase.4. The process of claim 1 , wherein R claim 1 , Rand Rrepresent H or a (C-C)alkyl radical.5. The process of claim 1 , wherein A is a radical of formula —CH—CH—CH(R′)— claim 1 , and R′ represents a (C-C)alkyl radical claim 1 , and preferably methyl or ethyl.6. The process of claim 1 , wherein R is H.7. The process of claim 1 , wherein the hydrogenation is carried out at a temperature greater than or equal to 105° C.9. The process of claim 1 , wherein the pressure is between 10 bar and 50 bar.10. The process of claim 1 , wherein R represents a linear or branched alkyl radical comprising from 1 to 10 carbon atoms.11. The process of claim 1 , wherein the hydrogenation catalyst is a mixture of at least two metals selected from the group consisting of ruthenium claim 1 , platinum claim 1 , palladium claim 1 , iridium and rhodium claim 1 , said mixture being supported by an inert substance.12. The process of claim 1 , wherein the hydrogenation catalyst ...

Подробнее
08-05-2014 дата публикации

2-Methylthiopyrrolidines and Their Use for Modulating Bacterial Quorum Sensing

Номер: US20140128446A1

Compounds of Formula (I) are disclosed herein and their use in inhibiting quorum sensing in bacteria. 2. The compound of claim 1 , wherein Ris OH and Ris H.3. The compound of claim 1 , wherein Rand Rtogether are oxo.43. The compound of any one of - claims 1 , wherein at least one of Rand Ris OH.5. The compound of claim 4 , wherein both Rand Rare OH.63. The compound of any one of - claims 1 , wherein both Rand Rare H.76. The compound of any one of - claims 1 , wherein X is S.86. The compound of any one of - claims 1 , wherein X is NR.9. The compound of claim 8 , wherein Ris H.10. The compound of claim 8 , wherein Ris C(O)alkyl.1110. The compound of any one of - claims 1 , wherein Ris C-Calkyl.1210. The compound of any one of - claims 1 , wherein Ris C-CalkyleneCOH.1310. The compound of any one of - claims 1 , wherein Ris C-CalkyleneCO—C-Calkyl.1410. The compound of any one of - claims 1 , wherein Ris C-CalkyleneCO-amino.1615. A pharmaceutical composition comprising the compound of any one of - and a pharmaceutically acceptable excipient.1715. A method of inhibiting bacterial quorum sensing comprising contacting bacteria with the compound of any one of - or the composition of .18Acinetobacter baumannii, Aeromonas hydrophila, Aeromonas salmonicida, Agrobacterium tumefaciens, Brucella melitensis, Burkholderia cenocepacia, Burkholderia mallei, Burkholderia pseudomallei, Burkholderia vietnamiensis, Chromobacterium violaceum, Enterobacter agglomeran, Erwinia carotovora, Erwinia chrysanthemi, Escherichia coli, Nitrosomas europaea, Obesumbacterium proteus, Pantoea agglomerans, Pantoea stewartii, Pseudomonas aureofaciens, Pseudomonas aeruginosa, Pseudomonas fluorescens, Pseudomonas fuscovaginae, Pseudomonas syringae, Ralstonia solanacearum, Rhizobium etli, Rhizobium leguminosarum, Rhodobacter sphaeroides, Serratia liquefaciens, Serratia marcescens, Vibrio anguillarum, Vibrio fischeri, Vibrio parahaemolyticus, Vibrio salmonicida, Xanthomonas campestris, Xenorhabdus ...

Подробнее
01-03-2018 дата публикации

IONIC LIQUID FOR FORWARD OSMOSIS PROCESS AND FORWARD OSMOSIS PROCESS

Номер: US20180056241A1

A forward osmosis process is provided, which includes separating a feed part and a draw solution part by a semi-permeable film. An ionic liquid is introduced into the draw solution part, and brine is introduced into the feed part. The brine has an osmotic pressure lower than that of the ionic liquid, so that pure water of the brine permeates through the semi-permeable film, enters the draw solution part, and mixes with the ionic liquid to form a draw solution. The draw solution was obtained out of the draw solution part to be left to stand at room temperature, so that the draw solution separated into a water layer and an ionic liquid layer. The ionic liquid includes 14-. (canceled)68-. (canceled)10. (canceled)12. (canceled)13. The forward osmosis process as claimed in claim 5 , further comprising introducing the ionic liquid layer into the draw solution part after the step of separating the draw solution into the water layer and the ionic liquid layer14. The forward osmosis process as claimed in claim 5 , wherein the step of introducing the brine into the feed part is continuously introducing seawater into the feed part.15. The forward osmosis process as claimed in claim 5 , further comprising a step of stirring the pure water and the ionic liquid in the draw solution part for mixing the pure water and the ionic liquid to form the draw solution. This application claims the benefit of U.S. Provisional Application No. 62/381,187 filed on Aug. 30, 2016, and claims priority from Taiwan Application Serial Number 105139655 filed on Dec. 1, 2016, the entirety of which are incorporated by reference herein.The technical field relates to a draw solute (ionic liquid) for a forward osmosis process.The technical principle of forward osmosis (FO) desalination process utilizes an osmosis pressure difference (between two solutions/solutes in two parts separated by a semi-permeable film) as a driving force. Water in a feed part with a lower osmosis pressure will permeate through a ...

Подробнее
01-03-2018 дата публикации

A POLAR ADDITIVE-CONTAINING HYDROPROCESSING CATALYST AND METHOD OF MAKING AND USING THEREOF

Номер: US20180057756A1
Принадлежит:

A method of making a hydroprocessing catalyst composition that includes impregnating a support material with metals and an organic acid compound followed by a controlled drying of the impregnated support and incorporation thereafter of a polar additive into the dried, impregnated support. The hydroprocessing catalyst is made by this method. 1. A method of making a hydroprocessing catalyst composition , wherein said method comprises:incorporating an impregnation solution, comprising a Group 9/10 metal component, a Group 6 metal component, and an organic acid compound, into a support material to provide an impregnated support material;drying said impregnated support material at a drying temperature that is in the range of from above the melting temperature of said organic acid compound and below the boiling temperature of said organic acid compound to provide a dried impregnated support material; andincorporating a polar additive having a dipole moment of at least 0.45 into said dried impregnated support material to thereby provide an additive-impregnated composition.2. A method as recited in claim 1 , wherein said organic acid compound is selected from the group of carboxylic compounds consisting of di or tri carboxylic acid compounds having at least 3 up to 10 carbon atoms and which may or may not be substituted with one or more hydroxyl groups claim 1 , wherein the molar mass of the carboxylic acid compound is in the range of from 100 to 250 g/mol claim 1 , the melting point of the carboxylic acid compound is in the range of from 100 to 200° C. claim 1 , and the carboxylic acid compound is soluble in water.3. A method as recited in claim 2 , wherein said organic acid compound is either gluconic acid or citric acid.4. A method as recited in claim 3 , wherein said impregnation solution is an aqueous solution including a metal salt of said Group 9/10 metal component that is selected from the group consisting of cobalt and nickel claim 3 , wherein said Group 9/10 metal ...

Подробнее
05-03-2015 дата публикации

PROCESS FOR MICROWAVE ASSISTED SYNTHESIS OF N-METHYL PYRROLIDONE

Номер: US20150065731A1
Принадлежит:

The present invention relates to a process for microwave assisted synthesis of N-methyl pyrrolidone (NMP). Particularly the process relates to the synthesis of N-methyl succinimide or corresponding analogues by using microwave irradiation which on hydrogenation in the presence of a hydrogenating catalyst gives N-methyl pyrrolidone. Compared to the conventional heating microwave process requires less energy inputs and reduces the reaction time drastically from 5-6 h to 2-5 min. 1. A process for synthesis of N-methyl pyrrolidone , said process comprising the steps of:(a) reacting a dicarboxylic acid or corresponding anhydride with non-aqueous methylamine with a molar ratio in the range 1:1 to 1:10 in solid state using microwave irradiation in the range of 600-900 W for a period of 1 to 10 minutes to obtain an intermediate N-methyl imide;(b) separating and purifying the intermediate N-methyl imide thus formed; and(c) converting the intermediate N-methyl imide to N-methyl pyrrolidone.2. The process according to claim 1 , wherein said dicarboxylic acid or anhydride is selected from the group consisting of maleic acid claim 1 , maleic anhydride claim 1 , succinic acid claim 1 , succinic anhydride and an analog thereof.3. The process according to claim 1 , wherein said non aqueous methylamine is selected from the group consisting of anhydrous methylamine claim 1 , methylamine in THF and methylamine hydrochloride.4. The process according to claim 1 , wherein an organic solvent is used for separating the intermediate N-methyl imide thus formed.5. The process according to claim 4 , wherein the organic solvent is selected from the group consisting of chloroform claim 4 , ethyl acetate claim 4 , dichloromethane and toluene.6. The process according to claim 1 , wherein purifying the intermediate N-methyl imide comprises subjecting the intermediate N-methyl imide to a crystallization process.7. The process according to claim 1 , wherein converting the intermediate N-methyl imide ...

Подробнее
12-06-2014 дата публикации

METHODS FOR PREPARATION OF AMMONIUM SALTS OF C4 DIACIDS BY FERMENTAION AND INTEGRATED METHODS FOR MAKING C4 DERIVATIVES

Номер: US20140162326A1
Автор: Ma Chicheng, Werpy Todd
Принадлежит:

Methods for forming ammonium salts of C4 diacids in a fermentation process with removal of divalent metal carbonate salts are disclosed. The pH of fermentation broths for production of C4 diacids is controlled by adding alkaline oxygen containing calcium or magnesium compounds, which forms divalent metal salts of the diacids. The divalent metal salts of the diacids are substituted with ammonium by introduction of ammonium salts at elevated temperature and pressure forming soluble ammonium salts thereof. C02 or bicarbonate is simultaneously added to the fennentation media at the elevated temperature and pressure. Reducing the temperature and pressure forms insoluble divalent metal carbonate salts that are separated from the solubilized ammonium diacid salts. 1. A method of making C4 acid derivative compound , comprising ,obtaining a clarified fermentation broth from growth of a microorganism to produce at least one diammonium salt of a C4 diacid selected from the group consisting of succinic, malic, maleic and fumaric acid; and{'sub': '2', 'contacting the clarified fermentation broth containing the diammonium salt of the C4 diacid with a hydrogenation catalyst and Hin a reaction mixture under conditions of temperature, pressure and time sufficient to hydrogenate the diammonium salt of the C4 diacid to form a derivative compound selected from the group consisting of -methyl-2-pyrrolidone (NMP), gamma-butyrolactone (GBL) and 1,4-butane-diol (BDO).'}2. The method of wherein the derivative compound is NMP claim 1 , and methanol is included in the clarified fermentation broth during the contacting with the hydrogenation catalyst.3. The method of wherein the derivative compound is GBL; C4 diacids in the fermentation broth comprise primarily succinate or are reduced to succinic acid during the hydrogenation; a dioxane solvent is included in the hydrogenation reaction mixture; and the hydrogenation catalyst for formation of the GBL comprises palladium and AlO.4. The method ...

Подробнее
12-05-2022 дата публикации

METHOD FOR PURIFYING WASTE N-METHYL-2-PYRROLIDONE MIXTURE SOLUTION

Номер: US20220144772A1
Автор: SHIM Sung Won
Принадлежит:

A method for purifying a waste N-methyl-2-pyrrolidone (NMP) mixed solution according to an embodiment of the present disclosure includes using a base. The base according to an embodiment may be NaBH. N-methylsuccinimide and γ-butyrolactone are simultaneously removed, and high-purity NMP can be recovered by applying a base to the waste NMP mixed solution. 1. A method for purifying waste N-methyl-2-pyrrolidone (NMP) mixed solution comprising N methylsuccinimide (NMS) and γ-butyrolactone (GBL) being a by-product of NMP , the method comprising:{'sub': '4', 'adding a base comprising NaBH(SBH) to the waste NMP mixed solution to perform a reaction of converting the NMS to 5-hydroxy-N-methyl-2-pyrrolidone and converting the GBL to 1,4-butanediol, whereby the NMS and the GBL are simultaneously removed.'}2. The method of claim 1 , wherein the SBH is added in an amount of 0.05 to 0.10 wt % based on the total weight of the waste NMP mixed solution.3. The method of claim 2 , wherein water is added in an amount of 5 to 20 wt % based on the total weight of the NMP mixed solution and the base claim 2 , a temperature of the reaction is 100 to 150° C. claim 2 , and the reaction is performed for 10 to 60 minutes.4. The method of claim 3 , wherein the SBH is dissolved in 10% concentration (w/v) NaOH and added to the waste NMP mixed solution.6. The method of claim 1 , wherein the waste NMP mixed solution is from a waste solution used in the secondary battery manufacturing process. This application claims benefit under 35 U.S.C. 119(e), 120, 121, or 365(c), and is a National Stage entry from International Application No. PCT/KR2020/008854, filed Jul. 7, 2020, which claims priority to the benefit of Korean Patent Application No. 10-2019-0082112 filed in the Korean Intellectual Property Office on Jul. 8, 2019, the entire contents of which are incorporated herein by reference.The present invention relates to a method for purifying a N-methyl-2-pyrrolidone (hereinafter referred to as NMP) ...

Подробнее
13-04-2017 дата публикации

PROCESS FOR PRODUCING QUATERNARY AMMONIUM CATIONS AND IONIC LIQUIDS

Номер: US20170101375A1
Принадлежит: CoorsTek Fluorochemicals, Inc.

The present invention provides a process and a method for producing a quaternary ammonium cation in an aqueous solution while reducing or preventing formation of a protonated ammonium cation. In particular, the quaternary ammonium cation is produced by adding a base to an aqueous reaction mixture comprising a tertiary amine compound and an alkylating agent. 1. A method for reducing the formation of a protonated tertiary amine cation during a process for producing a quaternary ammonium cation in an aqueous solution , said method comprising adding a base to an aqueous reaction mixture comprising a tertiary amine and an alkylating agent , wherein the pKa of a counter acid of said base is higher than the pKa of said protonated tertiary amine compound.2. The method of claim 1 , wherein the pKa of said counter acid of said base is higher than the pKa of said protonated amine compound by at least 1.3. The method of claim 2 , wherein the pKa of said counter acid of said base is higher than the pKa of said protonated amine compound by at least 2.4. The method of claim 1 , wherein the amount of said protonated tertiary amine compound produced is at least 80% less than a similar reaction condition in the absence of said base.5. The method of claim 1 , wherein said base comprises an alkaline metal hydroxide claim 1 , an alkaline earth metal hydroxide claim 1 , a transition metal hydroxide claim 1 , an alkaline metal oxide claim 1 , an alkaline earth metal oxide claim 1 , a transition metal oxide or a combination thereof.6. The method of claim 5 , wherein said base comprises sodium hydroxide claim 5 , potassium hydroxide claim 5 , calcium hydroxide claim 5 , lithium hydroxide claim 5 , cesium hydroxide claim 5 , magnesium hydroxide claim 5 , strontium hydroxide claim 5 , barium hydroxide claim 5 , lithium oxide claim 5 , sodium oxide claim 5 , potassium oxide claim 5 , cesium oxide claim 5 , magnesium oxide claim 5 , calcium oxide claim 5 , strontium oxide claim 5 , barium oxide ...

Подробнее
03-07-2014 дата публикации

PROCESS FOR THE TREATMENT OF A RECYCLYING STREAM FROM A PLANT FOR THE PRODUCTION OF POLYARYLENE ETHER SULFONES

Номер: US20140187796A1
Принадлежит: BASF SE

A process is proposed for the treatment of a recycling stream () from a plant for the production of polyarylene ether sulfones via polycondensation of aromatic bishalogen compounds and of aromatic bisphenols or their salts in the presence of at least one alkali metal carbonate or ammonium carbonate or alkali metal hydrogencarbonate or ammonium hydrogencarbonate in an N-alkyl-2-pyrrolidone as solvent, comprising 112-. (canceled)15. The process according to claim 13 , wherein the N-alkyl-2-pyrrolidone is N-ethyl-pyrrolidone or N-methylpyrrolidone.16. The process according to claim 13 , wherein two or three evaporator stages are provided.17. The process according to claim 16 , wherein the first evaporator stage is operated at a pressure in the vapor space in the range from 250 mbar absolute to atmospheric pressure claim 16 , such that from 70% to 90% of the water present in the recycling stream is drawn off by way of the vapor stream from the first evaporator stage claim 16 , said stream being introduced as feed stream into the final column.18. The process according to claim 17 , wherein the first evaporator stage is operated at a pressure in the vapor space in the range from 300 to 800 mbar absolute.19. The process according to claim 16 , wherein the second evaporator stage is operated at a pressure in the vapor space in the range from 250 to 500 mbar absolute claim 16 , such that from 90% to 95% claim 16 , of the N-alkyl-2-pyrrolidone present in the recycling stream is drawn off by way of the vapor stream from the second evaporator stage claim 16 , said stream being introduced as feed stream into the final column.20. The process according to claim 19 , wherein the second evaporator stage is operated at a pressure in the vapor space in the range from 300 to 400 mbar absolute.21. The process according to claim 13 , wherein the third evaporator stage is operated at a pressure in the vapor space in the range from 100 to 400 mbar absolute.22. The process according to ...

Подробнее
09-06-2022 дата публикации

METHOD FOR SYNTHESIZING LACTAM DERIVATIVES WITHOUT USE OF CATALYST

Номер: US20220177429A1
Автор: Li Hu, WU Hongguo, Yang Song
Принадлежит: GUIZHOU UNIVERSITY

Disclosed is a simple synthesis method of lactam derivatives, comprising: with formamide functioning as both an amine source and a hydrogen source (hydrolyzed to produce formic acid), carrying out a cycloamination reaction on a raw material keto acid in the absence of a solvent or a catalyst to simply synthesize a lactam derivative. Compared with previous reports, the present disclosure has the following advantages: the time required for the reaction is greatly shortened, the selectivity is remarkably improved, a conversion rate of a keto acid derivative is greater than 99%, and the yield of the lactam derivative can reach 70% to 94%. 1. A method for synthesizing lactam derivatives without use of a catalyst , comprising: carrying out a direct addition reaction between a raw material keto acid derivative and formamide functioning as both an amine source and a hydrogen source in the absence of an organic solvent or a catalyst , and then carrying out formic acid reduction and ring-closure reaction to obtain a corresponding lactam derivative.2. The method for synthesizing lactam derivatives without use of a catalyst according to claim 1 , wherein the preparation of the lactam derivative is carried out in water claim 1 , the reaction system is a closed system claim 1 , and the reaction is carried out for 60 to 300 min at a temperature within a range of 140° C. to 180° C.3. The method for synthesizing lactam derivatives without use of a catalyst according to claim 1 , wherein a molar ratio of the keto acid derivative to the formamide to water is 1:5˜15:10˜40.4. The method for synthesizing lactam derivatives without use of a catalyst according to claim 1 , wherein the keto acid derivative comprises levulinic acid claim 1 , 3-(4-chlorobenzoyl)propionic acid claim 1 , 3-benzoylpropionic acid claim 1 , 3-(4-fluorobenzoyl)propionic acid claim 1 , 4-oxo-4-(2-thienyl)butanoic acid claim 1 , acetobutyric acid claim 1 , 4-(4-fluorobenzoyl)butyric acid claim 1 , 4-benzoylbutyric ...

Подробнее
27-05-2021 дата публикации

Quaternary heteroatom containing compounds

Номер: US20210155592A1

The invention provides heterocyclic compounds with quaternary centers and methods of preparing compounds. Methods include the method for the preparation of a compound of Formula (II): comprising treating a compound of Formula (I): with a transition metal catalyst and under alkylation conditions as valence and stability permit.

Подробнее
19-05-2016 дата публикации

2-METHYLTHIOPYRROLIDINES AND THEIR USE FOR MODULATING BACTERIAL QUORUM SENSING

Номер: US20160137599A1
Принадлежит:

Compounds of Formula (I) are disclosed herein and their use in inhibiting quorum sensing in bacteria. 2. The compound of claim 1 , wherein Ris OH and Ris H.3. The compound of claim 1 , wherein Rand Rtogether are oxo.4. The compound of any one of - claim 1 , wherein at least one of Rand Ris OH.5. The compound of claim 4 , wherein both Rand Rare OH.6. The compound of any one of - claim 4 , wherein both Rand Rare H.7. The compound of any one of - claim 4 , wherein X is S.8. The compound of any one of - claim 4 , wherein X is NR.9. The compound of claim 8 , wherein Ris H.10. The compound of claim 8 , wherein Ris C(O)alkyl.11. The compound of any one of - claim 8 , wherein Ris C-Calkyl.12. The compound of any one of - claim 8 , wherein Ris C-CalkyleneCOH.13. The compound of any one of - claim 8 , wherein Ris C-CalkyleneCO—C-Calkyl.14. The compound of any one of - claim 8 , wherein Ris C-CalkyleneCO-amino.16. A pharmaceutical composition comprising the compound of any one of - and a pharmaceutically acceptable excipient.17. A method of inhibiting bacterial quorum sensing comprising contacting bacteria with the compound of any one of - or the composition of .18Acinetobacter baumannii, Aeromonas hydrophila, Aeromonas salmonicida, Agrobacterium tumefaciens, Brucella melitensis, Burkholderia cenocepacia, Burkholderia mallei, Burkholderia pseudomallei, Burkholderia vietnamiensis, Chromobacterium violaceum, Enterobacter agglomeran, Erwinia carotovora, Erwinia chrysanthemi, Escherichia coli, Nitrosomas europaea, Obesumbacterium proteus, Pantoea agglomerans, Pantoea stewartii, Pseudomonas aureofaciens, Pseudomonas aeruginosa, Pseudomonas fluorescens, Pseudomonas fuscovaginae, Pseudomonas syringae, Ralstonia solanacearum, Rhizobium etli, Rhizobium leguminosarum, Rhodobacter sphaeroides, Serratia liquefaciens, Serratia marcescens, Vibrio anguillarum, Vibrio fischeri, Vibrio parahaemolyticus, Vibrio salmonicida, Xanthomonas campestris, Xenorhabdus nemalophilus, Yersinia ...

Подробнее
26-05-2016 дата публикации

PROCESS AND INTERMEDIATES FOR THE SYNTHESIS OF 8-[-METHYL]-8-PHENYL-1,7-DIAZA-SPIRO[4.5]DECAN-2-ONE COMPOUNDS

Номер: US20160145256A1
Принадлежит:

This application discloses a novel process to synthesize 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds, which may be used, for example, as NK-1 inhibitor compounds in pharmaceutical preparations, intermediates useful in said process, and processes for preparing said intermediates; also disclosed is a process for removal of metals from N-heterocyclic carbine metal complexes. 2. The process of wherein Step (a) is carried out in the presence of up to two equivalents of added 4-methylbenzenesulfonic acid monohydrate.3. The process of either of or further comprising claim 1 , after step (a) and before step (b) claim 1 , a reducing step comprising: (i) contacting the reaction mixture with an aqueous phase comprising a reducing reagent under conditions suitable to reduce said metathesis catalyst; and (ii) separating the reaction mixture from the aqueous phase and any precipitate formed during Reducing Step (i).4. The process of wherein the aqueous phase of said reducing step part (i) further comprises a phase transfer catalyst.5. The process of wherein said phase transfer catalyst is a quaternary ammonium salt.6. The process of any of to wherein the ring-closing metathesis catalyst comprises a group 8 transition metal or a group 6 transition metal and a carbene ligand.12. The process of any of to wherein the reducing reagent used after Step (a) is: (i) one or more of NaSO claim 4 , NaSO claim 4 , NaSOH claim 4 , NaOC(O)H claim 4 , or NaHPO; (ii) a phosphorous acid; (iii) one or more of sodium hydride claim 4 , sodium borohydride claim 4 , or lithium aluminum hydride; (iv) a reduction carried out with hydrogen and a metal hydrogenation catalyst; (v) ascorbic acid or oxalic acid; (vi) hydrogen peroxide; or (vii) one or more of copper claim 4 , zinc claim 4 , iron or magnesium metal.13. The process of wherein the reducing reagent is sodium metabisulfite (NaSO) claim 12 , sodium sulfite (NaSO) claim 12 , sodium ...

Подробнее
08-06-2017 дата публикации

SYSTEM AND METHOD FOR ORGANIC SOLVENT PURIFICATION

Номер: US20170158635A1
Автор: TERASHI Ryosuke
Принадлежит: ORGANO CORPORATION

An organic solvent purification system that separates an organic solvent having a boiling point of more than 100° C. at 1 atm, such as N-methyl-2-pyrrolidone (NMP), from a liquid mixture containing the organic solvent and water and purifies the organic solvent includes: a heater that heats the liquid mixture; a pervaporation apparatus that includes a pervaporation membrane, and is provided at subsequent position of the heater, the pervaporation apparatus separating the organic solvent from the water; a vacuum evaporator to which the organic solvent collected from a concentration side of the pervaporation apparatus is supplied; and piping that supplies the heater with the organic solvent vaporized in the vacuum evaporator as a heat source of the heater. The heater heats the liquid mixture using concentration heat of the organic solvent vaporized by the vacuum evaporator. 1. An organic solvent purification system that separates an organic solvent having a boiling point of more than 100° C. at 1 atm from a liquid mixture containing water and the organic solvent , and purifies the organic solvent , the organic solvent purification system comprising:a heater that heats the liquid mixture;a pervaporation apparatus provided at subsequent position of said heater, the pervaporation apparatus including a pervaporation membrane and separating the organic solvent from the water;a vacuum evaporator to which the organic solvent collected from a concentration side of said pervaporation apparatus is supplied; andpiping that supplies said heater with the organic solvent vaporized in said vacuum evaporator as a heat source of said heater.2. The organic solvent purification system according to claim 1 , further comprising an ion exchanger provided at preceding position of said heater claim 1 , the ion exchanger carrying out ion exchange processing of the liquid mixture.3. The organic solvent purification system according to claim 1 , comprising a degassing apparatus provided at ...

Подробнее
04-09-2014 дата публикации

Process for Preparing 5-biphenyl-4-amino-2-methyl Pentanoic Acid

Номер: US20140249320A1
Принадлежит:

The present invention relates to pyrrolidin-2-ones according to the formula (1), or salts thereof, 3. A compound according to wherein the compound according to formula (2) claim 1 , or tautomer claim 1 , or salt thereof claim 1 , is in crystalline form.4. A compound according to wherein the compound according to formula (2-a) claim 2 , or tautomer claim 2 , or salt thereof claim 2 , is in crystalline form.5. A compound according to claim 1 , wherein in the compound of formula (2-a) R1 is hydrogen or a nitrogen protecting group selected from pivaloyl and t-butyloxycarbonyl (BOC).13. A process according to claim 6 , wherein R1 and R2 are hydrogen and R3 is an ethyl group. This application is a Divisional application of Ser. No. 13/333,437, filed Dec. 21, 2011, which is a Divisional application of Ser. No. 12/522,767, filed Jul. 10, 2009, which is a National Phase Application of PCT/EP2008/000142, filed Jan. 10, 2008, which claims benefit of EP 07/100,451.9, filed Jan. 10, 2008.The present invention relates to pyrrolidin-2-ones according to formula (1), or salts thereof,wherein R1 is hydrogen or a nitrogen protecting group, as defined herein, methods for their preparation and their use in the preparation of NEP-inhibitors, particularly in the preparation of N-(3-carboxyl-1-oxopropyl)-(4S)-(p-phenylphenylmethyl)-4-amino-(2R)-methyl butanoic acid ethyl ester, or salt thereof.Endogenous atrial natriuretic peptides (ANP), also called atrial natriuretic factors (ANF), have diuretic, natriuretic and vasorelaxant functions in mammals. The natural ANF peptides are metabolically inactivated, in particular by a degrading enzyme which has been recognized to correspond to the enzyme neutral endopeptidase (NEP, EC 3.4.24.11), which is also responsible for e.g. the metabolic inactivation of enkephalins.In the art biaryl substituted phosphonic acid derivatives are known which are useful as neutral endopeptidase (NEP) inhibitors, e.g. as inhibitors of the ANF-degrading enzyme in ...

Подробнее
21-05-2020 дата публикации

DISTILLATION APPARATUS FOR NMP

Номер: US20200155961A1

The present invention provides a distillation apparatus for NMP which is capable of regenerating a spent NMP recovered from a process for production of an electrode for lithium ion batteries on-site, in which the NMP can be purified in a simple and safe manner irrespective of variation in concentration of water in the raw material or throughput, and a recovery rate of the NMP can be further enhanced. The distillation apparatus for NMP according to the present invention comprises a raw material tank , a distillation column and a product tank , in which the distillation column is a side-cut type distillation column that comprises a top portion in which a liquid to be treated is separated into a high-concentration NMP and water comprising light-boiling components, a bottom portion in which a refluxed liquid in the distillation column is further subjected to distillation to separate the refluxed liquid into a high-purity NMP and the high-concentration NMP comprising high-boiling components, and a mid-stage portion from which the high-purity NMP is withdrawn as a side-cut vapor, and the distillation column is further provided at a rear stage thereof, with a condenser for condensing the high-purity NMP withdrawn as the side-cut vapor, and a flow control means for regulating an amount of a liquid of the high-purity NMP withdrawn from the condenser to the product tank. 1. A distillation apparatus for NMP in which a spent NMP comprising light-boiling components and high-boiling components as impurities is purified , said distillation apparatus comprising a raw material tank for storing the spent NMP as a liquid to be treated , a distillation column in which the liquid to be treated which is supplied from the raw material tank is subjected to distillation to obtain a purified high-purity NMP , and a product tank for storing the high-purity NMP obtained in the distillation column , in which:the distillation column is a side-cut type distillation column that comprises a top ...

Подробнее
21-05-2020 дата публикации

QUATERNARY HETEROATOM CONTAINING COMPOUNDS

Номер: US20200157049A1
Принадлежит:

The invention provides heterocyclic compounds with quaternary centers and methods of preparing compounds. Methods include the method for the preparation of a compound of Formula (II): 130-. (canceled)32. The compound of claim 31 , wherein Rand Rcombine to form a carbonyl group.33. The compound of claim 31 , wherein Rand Y combine to form a ring with Q claim 31 , the ring including between 3 and 12 ring atoms.34. The compound of claim 33 , wherein the ring includes between 4 and 7 ring atoms.37. The compound of claim 36 , wherein the compound comprises one of a (+) enantiomer of the compound or a (−) enantiomer of the compound in an enantiomeric excess of greater than 50%.39. The compound of claim 38 , wherein the compound comprises one of a (+) enantiomer of the compound or a (−) enantiomer of the compound in an enantiomeric excess of greater than 50%.40. The compound of claim 38 , wherein:{'sup': '1', 'Ris selected from halogen, alkyl, optionally substituted aralkyl, optionally substituted alkoxycarbonylalkyl, optionally substituted cyanoalkyl, and optionally substituted hydroxyalkyl; and'}{'sup': 6', '9', '10, 'R, R, and Rare independently selected at each occurrence from aralkyloxy, aralkoxycarbonyl, heteroaryloxy, acyl, arylcarbonyl, aralkylcarbonyl, arylsulfonyl, alkoxycarbonyl, and aryloxycarbonyl.'}41. The compound of claim 40 , wherein:{'sup': '6', 'X is —NR—;'}{'sup': 7', '7, 'Z is selected from —C(O)— and —CRR—;'}{'sup': 7', '7, 'A at each occurrence is —CRR—;'}{'sup': 10', '11', '11, 'W is selected from —NR— and —CRR—; and'}n is 0-2.42. The compound of claim 41 , wherein n is 1.43. The compound of claim 38 , wherein:X is —O—;{'sup': 7', '7, 'Z is selected from —C(O)— and —CRR—;'}{'sup': 7', '7, 'A at each occurrence is —CRR—;'}{'sup': 10', '11', '11, 'W is selected from —NR—, and —CRR—; and'}n is 0-2.45. The method of claim 44 , wherein:{'sup': '6', 'X is —NR—;'}{'sup': 7', '7, 'A at each occurrence is —CRR—;'}{'sup': 10', '11', '11, 'W is selected from — ...

Подробнее
21-06-2018 дата публикации

APPARATUS AND PROCESS FOR THE PREPARATION OF ACETYLENE AND SYNTHESIS GAS

Номер: US20180170829A1
Принадлежит: BASF SE

An apparatus () for the preparation of acetylene and synthesis gas by partial oxidation of hydrocarbons with oxygen is proposed. The apparatus () comprises a reactor (), wherein the reactor () comprises a burner block () with a furnace chamber for the preparation of a composition C comprising at least acetylene and substituted acetylene, a first scrubber () which is constructed for adding a solvent to the composition C to obtain a composition C, a second scrubber () which is constructed for adding the solvent to the composition C to obtain a composition C, a first stripper () which is constructed for stripping the composition C to obtain a composition C comprising the substituted acetylene, acetylene and the solvent and for separating off the acetylene, a first column () which is constructed for partial degassing of the composition C under a pressure of from 1.0 bar to 1.5 bar to obtain a composition C and a first amount A of the solvent, a second stripper () to which the composition C can be fed for stripping a composition C to obtain a second amount A of the solvent and a composition C, a third stripper () which is constructed for stripping the solvent from the first scrubber () to obtain a composition C, wherein the third striper () is connected to the second stripper () for feeding the composition C to the second stripper (), an apparatus () for adding a diluting gas to the composition C, which is arranged between the first column () and the second stripper (), a second column () which is constructed for adding water to the composition C to obtain a composition C comprising a third amount A of the solvent and water and to obtain a composition C comprising the substituted acetylene, and a mixing condenser () which is constructed for adding water to the composition C to obtain a composition C comprising the substituted acetylene. 1: An apparatus for preparation of acetylene and synthesis gas by partial oxidation of hydrocarbons with oxygen , comprising:{'b': '1', ...

Подробнее
02-07-2015 дата публикации

PYRROLIDINYL DERIVATIVES AS 11-BETA HYDROXYSTEROID DEHYDROGENASE INHIBITORS

Номер: US20150183735A1
Принадлежит:

The N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein 2. A compound according to wherein;n is 1;{'sub': 1', '1-4, 'L represents a C-linker optionally substituted with one or two Calkyl substituents'}{'sub': '1-2', 'M represents a Calkanediyl'}{'sup': '3', 'sub': 1-4', '1-4, 'Rrepresents hydrogen, halo, Calkyl, Calkyloxy- or cyano;'}{'sup': '4', 'sub': 1-4', '1-4, 'Rrepresents hydrogen, halo, Calkyl or Calkyloxy-;'}{'sup': 5', '2, 'sub': 1-4', '1-4, 'Rrepresents hydrogen, Calkyl or Ar—Calkyl;'}{'sup': '6', 'sub': '1-4', 'Rrepresents hydrogen, halo, or Calkyloxy;'}{'sup': '1', 'Arrepresents phenyl;'}{'sup': '2', 'Arrepresents phenyl or naphthyl.'}3. (canceled)4. A compound according to wherein M represents a C-linker.5. A compound according to wherein L represents a C-linker substituted with a Calkyl claim 1 , wherein said Calkyl is in the S-configuration.6. A compound as claimed in wherein the compound is selected from the group consisting of:3-[(6-Chloro-1,3-benzodioxol-5-yl)methyl]-1-(1-phenylethyl)-2-pyrrolidinone;an N-oxide, a pharmaceutically acceptable addition salt or a stereochemically isomeric form thereof.7. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and claim 1 , as active ingredient claim 1 , an effective 11β-HSD1 inhibitory amount of a compound as described in .8. A process of preparing a pharmaceutical composition as defined in claim 1 , characterized in that claim 1 , a pharmaceutically acceptable carrier is intimately mixed with an effective 11β-HSD1 inhibitory amount of a compound as described in .9. (canceled)10. A method for treating pathologies associated with excess cortisol formation claim 1 , comprising administering an effective amount of a compound as claimed in .11. The method of claim 10 , wherein the pathology associated with excess cortisol formation is selected from obesity claim 10 , diabetes claim 10 , obesity related cardiovascular ...

Подробнее
04-07-2019 дата публикации

NEW PROCESSES AND INTERMEDIATES FOR NEP INHIBITOR SYNTHESIS

Номер: US20190202785A1
Принадлежит:

The present invention relates to a new chemical synthesis, intermediates and catalysts useful for the preparation of the neprilysin (NEP) inhibitor sacubitril, inter alia via nitro 5 compounds. It further relates to new intermediate compounds and their use for said new chemical synthesis route, as well as a new catalyst ligand. 11. A process according to , wherein the compound of formula (1-a) is produced by a process according to any one of the to .13. A process according to , wherein the compound of formula (1-b) or the compound of formula (1-d) wherein R4 is hydrogen , is produced by a process according to any one of the to . The present invention relates to a new chemical synthesis route and intermediates useful for the preparation of neprilysin (NEP) inhibitors and their prodrugs, in particular for the NEP inhibitor prodrug sacubitril.The NEP inhibitor prodrug sacubitril (N-(3-carboxyl-1-oxopropyl)-(4S)-(p-phenylphenylmethyl)-4-amino-(2R)-methyl butanoic acid ethyl ester; IUPAC name 4-{[(1 S,3R)-1-([1,1′-Biphenyl]-4-ylmethyl)-4-ethoxy-3-methyl-4-oxobutyl]amino}-4-oxobutanoic acid) is represented by the following formula (A)Sacubitril together with valsartan, a known angiotensin receptor blocker (ARB), forms a sodium salt hydrate complex, known as LCZ696, comprising the anionic forms of sacubitril and valsartan, sodium cations and water molecules in the molar ratio of 1:1:3:2.5, respectively (ratio of 6:6:18:15 in the asymmetric unit cell of the solid state crystal), which is schematically present in formula (B).Said complex is also referred to by the following chemical names: Trisodium [3-((1S,3R)-1-biphenyl-4-ylmethyl-3-ethoxycarbonyl-1-butylcarbamoyl)propionate-(S)-3′-methyl-2′-(pentanoyl{2″-(tetrazol-5-ylate)biphenyl-4′-ylmethyl}amino)butyrate] hemipentahydrate or Octadecasodium hexakis(4-{[(1 S,3R)-1-([1,1′-biphenyl]-4-ylmethyl)-4-ethoxy-3-methyl-4-oxobutyl]amino}-4-oxobutanoate) hexakis(N-pentanoyl-N-{[2′-(1H-tetrazol-1-id-5-yl)[1,1′-biphenyl]-4-yl]methyl ...

Подробнее
05-08-2021 дата публикации

METHOD AND APPARATUS FOR RECOVERING AMIDE-BASED COMPOUND

Номер: US20210238137A1
Принадлежит:

The present disclosure provides a method and an apparatus for efficiently recovering an amide-based compound such as N-methyl-2-pyrrolidone from an aqueous solution containing an amide-based compound such as N-methyl-2-pyrrolidone. 1. A method for recovering an amide-based compound , comprising the steps of:(i) introducing a mixed solution containing water and an amide-based compound, and an extraction solvent, into an extraction region of a distillation column, wherein the distillation column is equipped with a dividing wall, and is divided into a column top region and a column bottom region in which the dividing wall is not located and a middle region in which the dividing wall is located, wherein the middle region is divided into the extraction region and a distillation region divided by the dividing wall,(ii) separating and discharging the amide-based compound and the extraction solvent into an upper stream of the extraction region in the distillation column, followed by separating water into a lower stream of the extraction region and discharging the water to a first outflow port located on the extraction region side in the column bottom region of the distillation column, and(iii) introducing at least one of the upper stream and the lower stream of the extraction region into the distillation region of the distillation column, followed by separating the extraction solvent into an upper stream of the distillation region and discharging the extraction solvent to a second outflow port of the column top region of the distillation column, separating the water into a middle stream of the distillation region and discharging the water to a third outflow port of the distillation region, and separating the amide-based compound into a lower stream of the distillation region and discharging the amide-based compound to a fourth outflow port located on the distillation region side in the column bottom region of the distillation column.2. The method for recovering an amide- ...

Подробнее
26-07-2018 дата публикации

OPHTHALMIC LENS MATERIAL AND OPHTHALMIC LENS OF SUCH MATERIAL

Номер: US20180210114A1
Автор: CHIEN HSIU-WEN
Принадлежит:

A wetness-retaining ophthalmic lens material comprises an organic monomer, a cross-linking agent, an initiator, a salt, and a solvent. The salt dissolves in the water dissociates a plurality of anions and cations, which bind to water molecules and retard the evaporation of the water molecules, the ophthalmic lens material thus can keep wet for a long time. An ophthalmic lens made of the ophthalmic lens material is also provided. 1. An ophthalmic lens material comprising:an organic monomer;a cross-linking agent;an initiator;a salt; anda solvent comprising water.2. The ophthalmic lens material of claim 1 , wherein the organic monomer has a mass percentage of about 32% to about 81% of the total mass of the ophthalmic lens material claim 1 , the cross-linking agent has a mass percentage of about 0.08% to about 14.6% of the total mass of the ophthalmic lens material claim 1 , the initiator has a mass percentage of about 0.05% to about 12.1% of the total mass of the ophthalmic lens material claim 1 , the salt has a mass percentage of about 3% to about 21.5% of the total mass of the ophthalmic lens material claim 1 , and the solvent has a mass percentage of about 5.5% to about 51% of the total mass of the ophthalmic lens material.3. The ophthalmic lens material of claim 1 , wherein the organic monomer comprises hydrophilic monomer claim 1 , the hydrophilic monomer is selected from a group consisting of 2-hydroxyethylmethacrylate claim 1 , methyl methacrylate claim 1 , N claim 1 ,N-dimethyacrylamide claim 1 , glycidyl methacrylate claim 1 , N-vinyl-2-pyrrolidone claim 1 , and any combination thereof.4. The ophthalmic lens material of claim 3 , wherein the organic monomer further comprises an organic silicon monomer claim 3 , the organic silicon monomer is selected from a group consisting of 3-(methacryloyloxy)propyltris(trimethylsiloxy)silane claim 3 , poly(dimethylsiloxane) claim 3 , and any combination thereof.5. The ophthalmic lens material of claim 1 , wherein the cross ...

Подробнее
09-08-2018 дата публикации

Process for the Selective Production of N-Methyl-2-Pyrrolidone (NMP)

Номер: US20180222859A1
Принадлежит:

This invention relates to an improved process for the selective production of N-methyl pyrrolidone (NMP) from gamma-butyrolactone and monomethyl amine preferably in aqueous form in the presence of a catalyst under comparatively milder conditions than the processes well known in the prior art of literature. The process is economically viable as it provides higher yield and selectivity for NMP which reduces the cost of separation of NMP from GBL. The catalyst shows good recyclability without significant loss in catalytic activity and no frequent regeneration is required. 110.-. (canceled)11. A process for the selective production of N-methyl-2-pyrrolidone (NMP) comprising:{'sub': 2', '2', '3, 'sup': '2', 'a) reacting feedstock monomethyl amine (MMA) and gamma-butyrolactone (GBL) in a single step in a continuously stirred tank reactor (CSTR) at a molar ratio of MMA to GBL in the range of 1 to 2, in the presence of catalyst consisting of a bronsted acidic support which is a class of zeolitic material with Si0to Al0molar ratio of 70 to 100 having specific surface area of 400 to 500 m/g and modified by oxide of one or metals selected from Al, Zr, W to the percentage of metal loading of 1 to 30 parts by weight of the support with catalyst content between 1 to 10% of total feedstock, at operating condition of temperature 130 to 250° C. and pressure 5 to 70 at 500 to 1000 agitator speed, for a period of 30 to 180 minutes to obtain a reaction mixture;'}b) cooling the reaction mixture to a temperature in the range of 20 to 25° C.;c) separating the catalyst from the reaction mixture of step b) by known methods;d) separating the product from reaction mixture of step c) by evaporation or distillation to obtain NMP at selectivity to ≥99% at a conversion of GBL to ≥98%; ande) recycling the catalyst to reactor after repeating the steps a) to d) several times.12. The process of claim 11 , wherein said MMA is in aqueous form.13. The process of claim 12 , wherein said MMA is in ...

Подробнее
30-07-2020 дата публикации

Levetiracetam Immunoassays

Номер: US20200240991A1
Принадлежит:

Methods, compositions and kits are disclosed directed at levetiracetam derivatives, immunogens, signal generating moieties, antibodies that bind levetiracetam and immunoassays for detection of levetiracetam. 147-. (canceled)49. The compound of claim 48 , wherein Z is the enzyme.50. The compound of claim 49 , wherein the enzyme is glucose-6-phosphate dehydrogenase (G6PDH).51. The compound of claim 49 , wherein the enzyme is selected from alkaline phosphatase claim 49 , β-galactosidase claim 49 , and horse radish peroxidase.52. The compound of claim 48 , wherein Z is the immunogenic carrier.53. The compound of claim 52 , wherein the immunogenic carrier is BSA or KLH.54. The compound of claim 52 , wherein the immunogenic carrier is selected from the group consisting of hemocyanins claim 52 , globulins claim 52 , albumins claim 52 , and polysaccharides.55. The compound of claim 52 , wherein the immunogenic carrier is selected from the group consisting of a protein claim 52 , a peptide claim 52 , a glycoprotein claim 52 , a saccharide claim 52 , a nucleic acid and a polynucleotide.56. A kit for determining an amount of levetiracetam in a medium claim 52 , wherein the kit comprises:{'claim-ref': {'@idref': 'CLM-00048', 'claim 48'}, 'a) an antibody that binds an epitope present in levetiracetam and a compound of ; and'}{'claim-ref': {'@idref': 'CLM-00048', 'claim 48'}, 'b) a compound of , wherein Z is the enzyme.'}57. The kit of claim 56 , wherein the enzyme is G6PDH.58. A reaction mixture comprising:a) a sample suspected of containing levetiracetam;{'claim-ref': {'@idref': 'CLM-00048', 'claim 48'}, 'b) an antibody that binds an epitope present in levetiracetam and a compound of ; and'}{'claim-ref': {'@idref': 'CLM-00048', 'claim 48'}, 'c) a compound of , wherein Z is the enzyme.'}59. The reaction mixture of claim 58 , wherein the enzyme is G6PDH.60. A method for detecting levetiracetam claim 58 , the method comprising:{'claim-ref': [{'@idref': 'CLM-00048', 'claim 48'}, ...

Подробнее
26-09-2019 дата публикации

2-ETHYLIDENE-1,5-DIMETHYL-3,3-DIPHENYLPYRROLIDINE ANALOGS AND METHODS FOR THEIR SYNTHESIS AND USE

Номер: US20190292148A1
Принадлежит: ALERE SAN DIEGO, INC.

The present invention relates to novel 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine analogs, and methods for their synthesis and use. Such analogs are designed to provide a convenient linkage chemistry for coupling under mild conditions to a suitable group on a target protein, polypeptide, solid phase or detectable label. 2. A compound or salt thereof according to claim 1 , wherein R2 is —(CH)—R3 claim 1 , wherein n is 0 to 6 and R3 is a functional moiety selected from the group consisting of protected or unprotected sulfhydryl moieties claim 1 , protected or unprotected amine moieties claim 1 , primary amine-reactive moieties claim 1 , sulfhydryl-reactive moieties claim 1 , photoreactive moieties claim 1 , carboxyl-reactive moieties claim 1 , arginine-reactive moieties claim 1 , and carbonyl-reactive moieties.3. A compound or salt thereof according to claim 1 , wherein the functional moiety is selected from the group consisting of a maleimide claim 1 , an alkyl halide claim 1 , an aryl halide claim 1 , an alpha-haloacyl claim 1 , an activated aryl claim 1 , a pyridyl disulfide claim 1 , a carbonyl claim 1 , a carboxyl claim 1 , a thiol claim 1 , a thioester claim 1 , disulfide claim 1 , or a cyclic thiolactone.6. A conjugate comprising one or more compounds according to covalently bound through the functional moiety on the compound(s) to a corresponding coupling site on a protein claim 1 , polypeptide claim 1 , detectable label claim 1 , nucleic acid claim 1 , or solid phase.7. A conjugate according to claim 6 , wherein the functional moiety is a sulfhydryl-reactive moiety.8. A conjugate according to claim 7 , wherein said sulfhydryl-reactive moiety is a maleimide.9. A conjugate according to claim 7 , wherein said sulfhydryl-reactive moiety is an alkyl halide claim 7 , an aryl halide claim 7 , an acryl claim 7 , or an α-haloacyl claim 7 , wherein the sulfhydryl-reactive moiety reacts with sulfhydryls to form thiol ether bonds.10. A conjugate according to claim ...

Подробнее
16-11-2017 дата публикации

ELECTRODE CURRENT COLLECTOR, METHOD OF MANUFACTURING THE SAME, ELECTRODE, LITHIUM ION SECONDARY BATTERY, REDOX FLOW BATTERY, AND ELECTRIC DOUBLE LAYER CAPACITOR

Номер: US20170331115A1
Принадлежит: SHOWA DENKO K.K.

An electrode current collector including a metal foil wherein a coating layer is formed on one or both surfaces of the metal foil, and a contact angle with pure water of the surface of the coating layer at a side opposite to the metal foil side is 30° or more. 1. An electrode current collector comprising a metal foil ,wherein a coating layer is formed on one or both surfaces of the metal foil, andthe coating layer comprises a conductive assistant, a water repellent material and a resin, wherein the resin is other than a water repellent material,a content of the water repellent material with respect to a total amount of the water repellent substance and the resin is 0.45% to 20% by mass, anda contact angle with pure water of a surface of the coating layer at a side opposite to the metal foil side is 30° or more.2. (canceled)3. The electrode current collector according to claim 1 ,wherein a content of the water repellent material with respect to a total amount of the water repellent substance and the resin is 5.0% to 20% by mass.4. The electrode current collector according to claim 1 ,wherein a content of the conductive assistant with respect to a total amount of the coating layer is 23% to 50% by mass.5. The electrode current collector according to claim 1 ,wherein the water repellent material is a fluorine-based polymer, andat least a part of the fluorine-based polymer is acid-modified.6. The electrode current collector according to claim 1 ,{'sup': 2', '2, 'wherein a coating weight per unit area of the coating layer is 0.1 g/mto 10 g/mper one coated surface.'}7. A method of manufacturing an electrode current collector according to claim 1 , comprising steps of:applying a slurry obtained by suspending the conductive assistant and the water repellent material in a solvent on one or both surfaces of the metal foil, anddrying the slurry coated on the metal foil,wherein the resin is other than a water repellent material.8. The method of manufacturing an electrode ...

Подробнее
29-11-2018 дата публикации

Quaternary heteroatom containing compounds

Номер: US20180339968A1

with a transition metal catalyst and under alkylation conditions as valence and stability permit.

Подробнее
31-12-2020 дата публикации

Bifunctional chiral organocatalytic compound having excellent enantioselectivity, preparation method therefor, and method for producing non-natural gamma-amino acid from nitro compound by using same

Номер: US20200406243A1
Автор: Deok-Chan HA, Jae Ho SHIM

The present invention relates to a bifunctional chiral organocatalytic compound having excellent enantioselectivity, a preparation method therefor, and a method for producing a non-natural gamma amino acid from a nitro compound by using the chiral organocatalytic compound. According to the present invention, the bifunctional chiral organocatalytic compound having excellent enantioselectivity can be easily synthesized, gamma-amino acids with high optical selectivity can be obtained at a high yield by an economical and convenient method using the chiral organocatalytic compound, and various (R)-configuration gamma-amino acids, which are not present in nature, can be produced with high optical purity in large quantities by using a small amount of a catalyst, and therefore, the present invention can be widely utilized in various industrial fields including the pharmaceutical industry.

Подробнее
10-11-2022 дата публикации

Levetiracetam Immunoassays

Номер: US20220357331A1
Принадлежит:

Methods, compositions and kits are disclosed directed at levetiracetam derivatives, immunogens, signal generating moieties, antibodies that bind levetiracetam and immunoassays for detection of levetiracetam. 147-. (canceled)49. The method of claim 48 , wherein the reaction mixture further comprises an antibody that binds an epitope present in levetiracetam and a compound of Formula 1.50. The method of claim 48 , wherein the enzyme is glucose-6-phosphate dehydrogenase (G6PDH).51. The method of claim 48 , wherein the enzyme is selected from alkaline phosphatase claim 48 , β-galactosidase claim 48 , and horse radish peroxidase.52. The method of claim 48 , wherein Ris —(CH)—NH—C(O)—(CH)—C(O)—Z.54. The method of claim 48 , wherein Ris —(CH)—NH—C(O)—(CH)—S—(CH)—C(O)—Z. This application claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Patent Application No. 61/108,369 filed Oct. 24, 2008, which is incorporated herein by reference in its entirety and for all purposes.The chemical name of levetiracetam, a single enantiomer, is (-)-(S)-α-ethyl-2-oxo-1-pyrrolidine acetamide, its molecular formula is CHNOand its molecular weight is 170.21. Levetiracetam is chemically unrelated to existing antiepileptic drugs (AEDs). It has the following structural formula:Situations in which AED therapeutic drug monitoring (“TDM”) are most likely to be of benefit have been described (49(7):1239-1276, 2008). They include (1) when a person has attained the desired clinical outcome, to establish an individual therapeutic concentration which can be used at subsequent times to assess potential causes for a change in drug response; (2) as an aid in the diagnosis of clinical toxicity; (3) to assess compliance, particularly in patients with uncontrolled seizures or breakthrough seizures; (4) to guide dosage adjustment in situations associated with increased pharmacokinetic variability (e.g., children, the elderly, patients with associated diseases, drug formulation changes); (5) when a ...

Подробнее
29-12-2022 дата публикации

Solvates Of Abscisic Acid And Liquid Compositions Containing Abscisic Acid

Номер: US20220411370A1
Принадлежит: CLARIANT INTERNATIONAL LTD.

The invention relates to new modifications of abscisic acid, to liquid compositions of abscisic acid and to their use in agrochemical applications. The modifications and compositions of the invention contain abscisic acid in the form of a solvate with at least one N-alkyl pyrrolidone, wherein the N-alkyl group has 3 to 6 carbon atoms. These solvates enable formulations with high concentrations of abscisic acid. 2. The solvate according to claim 1 , which is in an amorphous state.3. The solvate according to or claim 1 , wherein the abscisic acid is the naturally occurring form (S)-(+)-abscisic acid.5. The agrochemical composition according to claim 1 , comprising a solvate according to .6. The agrochemical composition according to claim 4 , wherein abscisic acid is (S)-(+)-abscisic acid.7. The agrochemical composition according to claim 4 , wherein the N-substituted pyrrolidone of formula (I) is N-n-butylpyrrolidone.9. The agrochemical composition according to claim 4 , wherein one or more formulation auxiliaries of component d) are selected from the group consisting of acidifiers claim 4 , adjuvants claim 4 , dispersing agents claim 4 , emulsifiers claim 4 , photodegradation stabilizer claim 4 , spontaneity agents and wetting agents.10. The agrochemical composition according to whereina) abscisic acid is present in an amount of 10 to 40% by weight, based on the total weight of the composition;b) the one or more N-substituted pyrrolidones are present in an amount of 10 to 90% by weight, based on the total weight of the composition;c) the one or more co-solvents are present in an amount of 0 or 0.1 to 30% by weight, based on the total weight of the composition; andd) the formulation auxiliaries are present in an amount of 0.1 to 35% by weight, based on the total weight of the composition; ande) the additional active compounds, incl. other derivatives of abscisic acid are present in an amount of 0 or 0.1 to 30% by weight, based on the total weight of the composition.12 ...

Подробнее
14-07-2004 дата публикации

Process

Номер: GB0412875D0
Автор: [UNK]
Принадлежит: Davy Process Technology Ltd

Подробнее
21-08-2020 дата публикации

一种长波长苯甲酰甲酸甲酯类光引发剂及其制备方法

Номер: CN111559963A
Автор: 朱晓群, 李阳, 聂俊

本发明涉及有机合成技术领域,尤其涉及一种长波长苯甲酰甲酸甲酯类光引发剂及其制备方法。目前市面上所使用的LED光源的发射波长范围均在365nm以上,而传统的光引发剂MBF的最大吸收波长为255nm,与LED光源的发射波长不相匹配,为了使得MBF光引发剂的最大吸收波长与LED光源的主要发射波长范围相匹配,本发明提供一种长波长苯甲酰甲酸甲酯类光引发剂,其由醛基和/或R 1 官能化的苯甲酰甲酸甲酯衍生物与含有αH原子的酮类化合物发生缩合反应得到,其最大吸收波长可以达到365nm以上,与市面上使用的LED光源相匹配,具有良好的商业应用前景。

Подробнее
02-02-2011 дата публикации

Process for the preparation of an N-alkyl lactam with improved colour quality

Номер: CN101415673B
Принадлежит: BASF SE

本发明涉及一种制备具有改进的颜色质量的N-烷基内酰胺的方法,其中向N-烷基内酰胺中加入0.01-10重量%C 1-10 醇或释放0.01-10重量%C 1-10 醇的化合物。本发明还涉及一种包含至少99.0重量%N-烷基内酰胺和100-5000重量ppm C 1-10 醇或释放100-5000重量ppm C 1-10 醇的缩醛、缩醛胺或原酸酯的混合物。

Подробнее
16-10-2018 дата публикации

一种锂电生产中nmp回收热泵精馏的方法及设备

Номер: CN108654130A

本发明提供一种锂电生产中NMP回收热泵精馏方法及设备,方法包括用水吸收NMP废气,得到NMP废液;将NMP废液输送至第一脱水精馏塔进行分离;将第一脱水精馏塔的塔釜采出的重组分输送至第二脱水精馏塔进行分离;将第二脱水精馏塔的塔釜采出重组分输送至NMP精馏塔进行分离,还将第一脱水精馏塔的塔顶轻组分气体经压缩机升压升温为高压饱和蒸汽,作为NMP精馏塔塔釜再沸器的热源。该方法可将锂电池生产中挥发NMP废气回收并提纯得到电子级NMP溶剂,直接用作锂电池生产中正负极材料的溶剂,提高NMP的利用度;精馏与热泵技术耦合,将精馏装置塔顶蒸汽的热能由低品位热能转化为高品位热能,用作塔釜再沸器的热源,充分利用设备中废气的能量,降低设备整体能耗。

Подробнее
06-11-2020 дата публикации

N-methyl pyrrolidone for liquid crystal panel and production process thereof

Номер: CN111892525A
Принадлежит: Myj Chemical Co ltd

本发明公开了一种液晶面板用N‑甲基吡咯烷酮的生产工艺,包括反应段、间歇提纯段、气提提纯段和二级精馏提纯段,不经过传统的纤维过滤,完全通过对反应原料、反应过程和提纯过程的创新以及工艺参数的严格控制,实现了N‑甲基吡咯烷酮产品达到SEMI C8的标准,再经过加压吸附过滤之后产品质量基本可以达到SEMI C12的标准。

Подробнее
12-01-2022 дата публикации

Enantionselective processes to insecticidal 3-aryl-3-trifluoromethyl-substituted pyrrolidines

Номер: EP3896058A3
Принадлежит: SYNGENTA PARTICIPATIONS AG

The present invention relates to processes for the enantio-selective preparation of spyrrolidine derivatives useful in the manufacture of pesticidally active compounds, as well as to intermedates in the processes. The processes include those comprising (a-i) reacting a compound of formula Ia wherein P is alkyl, aryl or heteroaryl, each optionally substituted, wherein the heteroaryl is connected at P via a ring carbon atom; R 1 is chlorodifluoromethyl or trifluoromethyl; R 2 is aryl or heteroaryl, each optionally substituted; with a source of cyanide in the presence a chiral catalyst to give a compound of formula IIa wherein P, R 1 and R 2 are as defined for the compound of formula Ia; and (a-ii) oxidising the compound of formula IIa with a peroxy acid, or peroxide in the presence of an acid to give a compound of formula VI wherein R 1 and R 2 are as defined for the compound of formula Ia.

Подробнее
27-12-2012 дата публикации

METHOD FOR PRODUCING N-ALKYLACTAM POSSESSING IMPROVED COLOR QUALITY

Номер: RU2011125705A
Принадлежит: БАСФ СЕ

1. Способ очистки N-алкиллактамов формулы Iв которой R означаетлинейный или разветвленный, насыщенный алифатический C-C-алкильный радикал илинасыщенный циклоалифатический радикал, содержащий от 3 до 12 атомов углерода,и n является целым числом, равным от 1 до 5, и где атомы углерода гетероциклического кольца N-замещенного лактама могут содержать от 1 до 2 С-С-алкильных радикалов, который предусматривает взаимодействие N-алкиллактамов с углем и отделение N-алкиллактама от угля.2. Способ получения смеси, обладающей йодным цветовым числом, измеренным в соответствии с DIN 6162, равным менее 500, содержащей по-ли(винилиденфторид) (ПВДФ) и 2-пирролидон или N-алкиллактам формулы Iв которой R означаетлинейный или разветвленный насыщенный алифатический C-C-алкильный радикал или насыщенный циклоалифатический радикал, содержащий от 3 до 12 атомов углерода, и n является целым числом, равным от 1 до 5, и где атомы углерода гетероциклического кольца N-замещенного лактама могут содержать от 1 до 2 C-C-алкильных радикалов, предусматривающийa) очистку 2-пирролидона или N-алкиллактама путем взаимодействия 2-пирролидона или N-алкиллактама с адсорбентом иb) смешивание очищенного 2-пирролидона или N-алкиллактама, полученного на стадии а), с ПВДФ, и в котором адсорбентом является уголь.3. Способ по п.2, в котором на стадии b) содержание ПВДФ составляет от 1 до 95 мас.% в пересчете на N-алкиллактам или 2-пирролидон.4. Способ по п.2, в котором на стадии b) содержание ПВДФ составляет от 1 до 50 мас.% в пересчете на N-алкиллактам или 2-пирролидон.5. Способ по п.2, в котором N-алкиллактамом является N-метилпирролидон (NMP) и/или N-этилпирролидон (NEP).6. Способ по п.2, в котором адсорбент обла РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) 2011 125 705 (13) A (51) МПК C07D 207/267 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ЗАЯВКА НА ИЗОБРЕТЕНИЕ (21)(22) Заявка: 2011125705/04, 18.11.2009 (71) Заявитель(и): БАСФ СЕ (DE) Приоритет(ы): (30) Конвенционный приоритет: 24.11.2008 EP ...

Подробнее
05-03-2021 дата публикации

Method for continuously synthesizing N-methyl pyrrolidone and N-ethyl pyrrolidone

Номер: CN107474003B

一种连续合成N‑甲基吡咯烷酮和N‑乙基吡咯烷酮的方法,该方法在微反应器中进行,将γ‑丁内酯溶液和相应的烷基胺溶液连续地通过一个微反应器,合成N‑甲基吡咯烷酮和N‑乙基吡咯烷酮。其中,微反应器包括反应段和反应抑制段,以及反应混合物在反应段的停留时间为1~30分钟条件下进行,并且,其中所述的γ‑丁内酯溶液和相应的烷基胺溶液都以乙二醇为溶剂,反应混合物中烷基胺和γ‑丁内酯的摩尔配比为1.0~1.6,所述的γ‑丁内酯溶液浓度为0.5~2mol/L。本发明可将N‑甲基吡咯烷酮和N‑乙基吡咯烷酮的合成过程时间由原来的数小时缩短至30min之内,同时产品的收率达到90%以上。

Подробнее
03-12-2018 дата публикации

Device and method for producing acetylene and synthesis gas

Номер: RU2673890C2
Принадлежит: БАСФ СЕ

FIELD: chemistry. SUBSTANCE: invention relates to a device for producing acetylene and synthesis gas by partial oxidation of hydrocarbons with oxygen. Device includes: a reactor equipped with a burner block with a combustion chamber to obtain composition Z1 containing at least acetylene and substituted acetylene, a first scrubber configured to mix composition Z1 with a solvent to obtain composition Z2, a second scrubber configured to mix composition Z2 with a solvent to obtain composition Z3, a first stripper for stripping composition Z3 to obtain composition Z4, containing substituted acetylene, acetylene and solvent, as well as for the separation of acetylene, a first column for partial degassing of composition Z4 at pressure from 1.0 to 1.5 bar to obtain composition Z5, composition Z10 and first portion A1 of the solvent, a second stripper, in which composition Z5 can be fed for stripping composition Z9 to obtain second portion A2 of the solvent and composition Z6, a third stripper for stripping the solvent from the first scrubber to obtain composition Z9, wherein in order to supply the composition Z9 to the second stripper, the third stripper is connected to the second stripper. Between the first column and the second stripper, there is a device for mixing composition Z5 with a diluent gas, a second column for mixing composition Z6 with water to obtain composition Z7 containing third portion A3 of the solvent and water, and also to obtain composition of Z8 containing substituted acetylene, and a mixing condenser configured to mix composition Z8 with water to obtain composition Z11 containing substituted acetylene. Also described is a method for producing acetylene and synthesis gas by the partial oxidation of hydrocarbons with oxygen. EFFECT: use of the present invention allows the process to be carried out under normal or slightly excess pressure without using a vacuum. 17 cl, 1 dwg РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 673 890 C2 (51) МПК C07C 2/78 (2006.01 ...

Подробнее
23-07-2019 дата публикации

New compound and the modified conjugated diene quasi polymer comprising the functional group from the compound

Номер: CN110049967A
Принадлежит: LG Chemical Co Ltd

本发明涉及一种由式1表示的化合物、其制备方法,以及包含来自所述化合物的官能团的具有高改性比的改性共轭二烯类聚合物。

Подробнее
04-09-1979 дата публикации

Manufacture of 22pyrrolidone

Номер: JPS54112858A
Принадлежит: Stamicarbon BV

Подробнее
01-04-1998 дата публикации

Process for preparing pyrroli donone derivatie

Номер: KR0127750B1
Автор: 김덕규
Принадлежит: 동아제약 주식회사, 손정삼

Halolactone compound(II) was reacted with NH2CH2R at 40-200deg.C for 4-30 hours in a solvent such as tetrahydrofuran, acetonitrile, dimethylformamide, ethyl alcohol and dimethylsulfoxide in the presence of a strong base such as sodium hydride, potassium hydride, triethylamine, and N,N-dimethylamine to give an intermediate compound(IV), which was refined with silica gel column chromatography or a cationic resin to obtain the pharmaceutically useful title compound (I), where R is alkoxy, substituted or nonsubstituted phenoxy, benzyl, or COR2; R2 is alkoxy, amine, diisopropyl ethylene amine, alkyl or alkoxyamine; R1 is H or OH-protectable tetrahydrofuran or acetyl; X is a halogen atom such as Cl, Br or I.

Подробнее
28-09-2018 дата публикации

Patent RU2016141836A3

Номер: RU2016141836A3
Автор: [UNK]
Принадлежит: [UNK]

ВИ“? 2016141836” АЗ Дата публикации: 28.09.2018 Форма № 18 ИЗ,ПМ-2011 Федеральная служба по интеллектуальной собственности Федеральное государственное бюджетное учреждение ж 5 «Федеральный институт промышленной собственности» (ФИПС) ОТЧЕТ О ПОИСКЕ 1. . ИДЕНТИФИКАЦИЯ ЗАЯВКИ Регистрационный номер Дата подачи 2016141836/04(066994) 25.03.2015 РСТ/ЕР2015/056377 25.03.2015 Приоритет установлен по дате: [ ] подачи заявки [ ] поступления дополнительных материалов от к ранее поданной заявке № [ ] приоритета по первоначальной заявке № из которой данная заявка выделена [ ] подачи первоначальной заявки № из которой данная заявка выделена [ ] подачи ранее поданной заявки № [Х] подачи первой(ых) заявки(ок) в государстве-участнике Парижской конвенции (31) Номер первой(ых) заявки(ок) (32) Дата подачи первой(ых) заявки(ок) (33) Код страны 1. 14161692.0 26.03.2014 ЕР* Название изобретения (полезной модели): [Х] - как заявлено; [ ] - уточненное (см. Примечания) УСТРОЙСТВО И СПОСОБ ПОЛУЧЕНИЯ АЦЕТИЛЕНА И СИНТЕЗ-ГАЗА Заявитель: БАСФ СЕ, ОЕ 2. ЕДИНСТВО ИЗОБРЕТЕНИЯ [Х] соблюдено [ ] не соблюдено. Пояснения: см. Примечания 3. ФОРМУЛА ИЗОБРЕТЕНИЯ: [Х] приняты во внимание все пункты (см. Примечания) [ ] приняты во внимание следующие пункты: [ ] принята во внимание измененная формула изобретения (см. Примечания) 4. КЛАССИФИКАЦИЯ ОБЪЕКТА ИЗОБРЕТЕНИЯ (ПОЛЕЗНОЙ МОДЕЛИ) (Указываются индексы МПК и индикатор текущей версии) С07С 2/78 (2006.01) С07С 11/24 (2006.01) СО1В 3/36 (2006.01) ВО1.] 7/00 (2006.01) 5. ОБЛАСТЬ ПОИСКА 5.1 Проверенный минимум документации РСТ (указывается индексами МПК) С07С 2/78, С07С 11/24, СОЛВ 3/36, ВО11 7/00 5.2 Другая проверенная документация в той мере, в какой она включена в поисковые подборки: 5.3 Электронные базы данных, использованные при поиске (название базы, и если, возможно, поисковые термины): ЕАРАТГУ, Езрасепе, ]-Р1а Раг, Раеагсв, КОРТО, ИЗРТО 6. ДОКУМЕНТЫ, ОТНОСЯЩИЕСЯ К ПРЕДМЕТУ ПОИСКА Кате- Наименование документа с указанием (где необходимо) частей, Относится ...

Подробнее
27-12-1995 дата публикации

Transvinylation process

Номер: RU2051143C1

FIELD: organic chemistry. SUBSTANCE: the product: a Brensted acid vinyl derivative, purity is 99% Reagent 1: a Brensted acid vinyl derivative selected from the group consisting of vinyl esters of saturated or unsaturated carboxylic acid. Reagent 2: the other Brensted acid. Reaction conditions: in the presence of a ruthenium compound as a catalyst at its concentration of from 30,000 to 0.23 ppm based on the weight of a liquid phase reaction mixture. The Brensted acid to ruthenium molar ratio is maintained at 0.9 to 1 at a temperature of from 75 to 259 C and at a pressure of from 10 to 2644.8 mm Hg. EFFECT: more efficient transvinylation process. 12 cl, 4 tbl СУСС ПЧ Го РОССИЙСКОЕ АГЕНТСТВО ПО ПАТЕНТАМ И ТОВАРНЫМ ЗНАКАМ (19) (51) МПК ВИ” 2 051 143. 13) Сл С 07С 69/00, 67/10 12) ОПИСАНИЕ ИЗОБРЕТЕНИЯ К ПАТЕНТУ РОССИЙСКОЙ ФЕДЕРАЦИИ (21), (22) Заявка: 4614352/04, 29.06.1989 (30) Приоритет: 30.06.1988 Ц$ 213697 (46) Дата публикации: 27.12.1995 (56) Ссылки: 1. Журнал органической химии, 1949, М 14, с.1057-1077.2. Тегапечдгоп, 1972, 28, р.227-232.3. Спет Вег. 1969, с.2929-2950.4. Патент Ц$ М 3755387, кл. С 07С 67/02, опублик. 1973. (71) Заявитель: Юнион Карбид Корпорейшн (1$) (72) Изобретатель: Рекс Юджин Муррей[Ц$] (73) Патентообладатель: Юнион Карбид Корпорейшн (1$) (54) СПОСОБ ПЕРЕВИНИЛИРОВАНИЯ (57) Реферат: Сущность изобретения: продукт - винилпроизводное КИСЛОТЫ Бренстеда. Чистота 99% Реагент 1: винилпроизводное кислоты Бренстеда, выбранное из группы сложных виниловых эфиров насыщенной или ненасыщенной карбоновой кислоты. Реагент 2: другая кислота Бренстеда. Условия реакции: в присутствии соединения рутения в качестве катализатора при его концентрации от 30,000 до 0,23 ч/млн. от веса жидкофазной реакционной смеси при молярном соотношении кислоты Бренстера и рутения 0,5/1 при температуре /5-259°С и давлении от 10 до 2644,8 мм рт.ст. 11 3. п. ф-лы, 4 табл. 2051143 С1 КО СУСС ПЧ Го КУЗЗАМ АСЕМСУ ГОК РАТЕМТ$ АМО ТКАОЕМАКК$ 13) ВУ” 2051 143 ^С1 (51) 1пё С1.6 с 07 с 69/00, 67 ...

Подробнее
09-01-2012 дата публикации

Process for preparing of n-methyl pyrrolidone from 1,4-butanediol

Номер: KR101103512B1

본 발명은 감마 부티로락톤 및 N-메틸 피롤리돈의 제조방법에 관한 것으로, 보다 상세하게는 1,4-부탄디올(BDO)을 반응기로 도입하여 금속산화물 촉매 하에서 탈수소화 반응으로 감마-부티로락톤(GBL)을 제조하고, 생성된 감마-부티로락톤과 추가 원료인 모노메틸아민(MMA) 수용액을 반응기로 공급하여 상기 모노메틸아민과 감마-부티로락톤의 반응에 의해 생성된 N-메틸 피롤리돈(NMP)과 물을 분리하고, 분리된 물은 모노메틸아민과 혼합하여 상기 모노메틸아민 수용액을 제조하여 반응기로 도입하는 N-메틸 피롤리돈(NMP)의 제조방법에 관한 것이다. The present invention relates to a method for preparing gamma butyrolactone and N-methyl pyrrolidone. More specifically, 1,4-butanediol (BDO) is introduced into a reactor to gamma-butyro by dehydrogenation under a metal oxide catalyst. Lactone (GBL) was prepared, and the resulting gamma-butyrolactone and additional raw material monomethylamine (MMA) aqueous solution were supplied to the reactor, and N-methyl produced by the reaction of the monomethylamine and gamma-butyrolactone. Pyrrolidone (NMP) and water is separated, and the separated water is mixed with the monomethylamine to prepare the monomethylamine aqueous solution to introduce a method for producing N-methyl pyrrolidone (NMP) introduced into the reactor. 본 발명에 따른 N-메틸 피롤리돈의 제조방법은 부탄디올로부터 촉매하에서 감마-부티로락톤(GBL)을 제조하고, 모노메틸아민과 감마-부티로락톤의 반응에 의해 생성된 물을 회수하여 모노메틸아민 수용액을 제조한 후 다시 반응기로 재공급하여 에너지를 절약할 뿐만 아니라 생성물인 N-메틸 피롤리돈을 쉽게 분리할 수 있는 장점이 있다. In the method for preparing N-methyl pyrrolidone according to the present invention, gamma-butyrolactone (GBL) is prepared from butanediol under a catalyst, and water produced by the reaction of monomethylamine and gamma-butyrolactone is recovered by mono After preparing the aqueous methylamine solution, it is supplied back to the reactor to save energy, and there is an advantage of easily separating the product, N-methyl pyrrolidone. N-메틸 피롤리돈, 감마-부티로락톤, 모노메틸아민, 금속산화물 촉매 N-methyl pyrrolidone, gamma-butyrolactone, monomethylamine, metal oxide catalyst

Подробнее
24-11-2020 дата публикации

Device for improving purity of NMP crude product after methylamine removal

Номер: CN111978233A

本发明属于NMP纯化技术领域,具体涉及一种提高脱甲胺后NMP粗品纯度的装置,所述脱甲胺后NMP粗品包括NMP、水和杂质,所述装置包括NMP纯化单元,所述NMP纯化单元包括NMP脱轻工段、NMP精制工段、电子级NMP中间存储工段,所述NMP脱轻工段、NMP精制工段、电子级NMP中间存储工段依次相连;所述脱甲胺后NMP粗品经过NMP脱轻工段处理后,NMP、水、较重的杂质进入NMP精制工段,经过NMP精制工段处理后,NMP进入电子级NMP中间存储工段。本发明的有益效果是脱甲胺后NMP粗品(NMP、水、杂质)经过依次经过NMP脱轻工段、NMP精制工段处理,进入电子级NMP中间罐内,对电子级NMP中间罐内NMP检测,其中甲胺含量≤5ppm,水分含量≤0.02%,pH在7‑9之间,色度≤10,完全符合电子级NMP的要求。

Подробнее
26-01-1995 дата публикации

Transuinylation reaction

Номер: KR950000643B1

내용 없음. No content.

Подробнее
20-11-2018 дата публикации

A kind of separation N-Methyl pyrrolidone/chloroform system and method

Номер: CN105693585B
Автор: 崔庆海, 庹新林

本发明属化学工程技术领域,特别涉及一种分离N‑甲基吡咯烷酮(NMP)/氯仿的系统及方法。本发明一种分离N‑甲基吡咯烷酮(NMP)/氯仿的系统将降膜蒸发器,强制循环蒸发器以及精馏塔有机结合,结合配套的工艺操作方法,不仅可以保证分离出的氯仿不会变质,而且回收的NMP纯度高。

Подробнее
29-04-2010 дата публикации

Levetiracetam immunoassays

Номер: WO2010048423A1
Принадлежит: Ark Diagnostics, Inc.

Methods, compositions and kits are disclosed directed at levetiracetam derivatives, immunogens, signal generating moieties, antibodies that bind levetiracetam and immunoassays for detection of levetiracetam.

Подробнее
06-10-2005 дата публикации

Use of N-ethyl-2-pyrrolidone

Номер: DE102004012751A1
Принадлежит: BASF SE

Verwendung von N-Ethyl-2-pyrrolidon als Lösungsmittel, Verdünnungsmittel, Extraktionsmittel, Reinigungsmittel, Entfettungsmittel, Absorptionsmittel und/oder Dispergierungsmittel, insbesondere als teilweiser oder vollständiger Ersatz für N-Methyl-2-pyrrolidon (NMP), chlorierte Kohlenwasserstoffe und/oder Ether.

Подробнее
11-11-2021 дата публикации

Low toxicity nmp substitutes and their preparation

Номер: WO2021163348A3
Принадлежит: ANGUS Chemical Company

The present technology is directed to compounds Formulas I, II, III, and IV as well as compositions that include one or more of the compounds and methods of making the compounds. In particular, the present compounds may be used as a replacement for NMP in compositions to produce lower toxicity compositions.

Подробнее
04-01-2012 дата публикации

N-substituted pyrrolidonium ionic liquids with expanded linker

Номер: CN102307856A
Принадлежит: EI Du Pont de Nemours and Co

本发明涉及可用作离子液体的化合物,所述化合物基于N-取代的吡咯烷酮并掺入通过可调节长度的连接子与吡咯烷酮环间隔的侧铵阳离子。

Подробнее
28-02-1996 дата публикации

Process for the preparation of optically active 4-amino-3-hydroxycarboxylic acids

Номер: EP0529483B1
Принадлежит: Lonza AG

Подробнее
20-11-1996 дата публикации

Process for purifying crude n-vinylpyrrolid-2-one

Номер: RU95102320A
Принадлежит: Басф Аг, Басф Аг (De)

Объектом изобретения является способ очистки сырого N-винилпирролид-2-она путем обработки последнего кислым реагентом, в качестве которого используют ангидрид органической карбоновой кислоты.

Подробнее
26-10-2021 дата публикации

Synthesis process of N-ethyl pyrrolidone

Номер: CN113548996A
Принадлежит: Jiangxi Shengyuan New Material Co ltd

本发明公开了一种N‑乙基吡咯烷酮的合成工艺,包括以下步骤:(1)将原料γ‑丁内酯和一乙胺通过计量泵加入到预热器中预热;(2)预热完成后所述γ‑丁内酯和所述一乙胺再进行均匀混合得混合物料;(3)将所述混合物料继续升温,升温后反应1.5~2小时,充分反应后得反应产物;(4)所述反应产物先降温冷却至40~60℃,再降压处理,最后进入脱胺塔去除过量一乙胺和水。本发明采用上述结构的一种N‑乙基吡咯烷酮的合成工艺,反应时间短,无需使用催化剂,降低成本,并且反应完成后由高压降低常压,提高反应的安全性。

Подробнее
26-04-2018 дата публикации

DEVICE AND METHOD FOR PRODUCING ACETHYLENE AND SYNTHESIS GAS

Номер: RU2016141836A
Принадлежит: БАСФ СЕ

РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2016 141 836 A (51) МПК C07C 2/78 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ЗАЯВКА НА ИЗОБРЕТЕНИЕ (21)(22) Заявка: 2016141836, 25.03.2015 (71) Заявитель(и): БАСФ СЕ (DE) Приоритет(ы): (30) Конвенционный приоритет: 26.03.2014 EP 14161692.0 (85) Дата начала рассмотрения заявки PCT на национальной фазе: 26.10.2016 (86) Заявка PCT: (87) Публикация заявки PCT: WO 2015/144754 (01.10.2015) R U (54) УСТРОЙСТВО И СПОСОБ ПОЛУЧЕНИЯ АЦЕТИЛЕНА И СИНТЕЗ-ГАЗА (57) Формула изобретения 1. Устройство (10) для получения ацетилена и синтез-газа путем частичного окисления углеводородов кислородом, включающее: реактор (12), снабженный блоком горелки (14) с топочной камерой для получения состава Z1, содержащего по меньшей мере ацетилен и замещенный ацетилен, первый скруббер (22), выполненный для смешивания состава Z1 с растворителем с получением состава Z2, второй скруббер (26), выполненный для смешивания состава Z2 с растворителем с получением состава Z3, первый отпарной аппарат (36), выполненный для отпаривания состава Z3 с получением состава Z4, содержащего замещенный ацетилен, ацетилен и растворитель, а также для выделения ацетилена, первую колонну (46), выполненную для частичной дегазации состава Z4 под давлением от 1,0 до 1,5 бар с получением состава Z5, состава Z10 и первой части А1 растворителя, второй отпарной аппарат (56), в который можно подавать состав Z5 для отпаривания состава Z9 с получением второй части А2 растворителя и состава Z6, третий отпарной аппарат (68), выполненный для отпаривания растворителя из первого скруббера (22) с получением состава Z9, причем для подачи состава Z9 во второй отпарной аппарат (56) третий отпарной аппарат (68) соединен со вторым Стр.: 1 A 2 0 1 6 1 4 1 8 3 6 A Адрес для переписки: 105064, Москва, а/я 88, "Патентные поверенные Квашнин, Сапельников и партнеры" 2 0 1 6 1 4 1 8 3 6 EP 2015/056377 (25.03.2015) R U (43) Дата публикации заявки: 26.04.2018 Бюл. № 12 (72) Автор(ы): ...

Подробнее
08-03-2006 дата публикации

Method for the production of a purified melt of at least one monomer

Номер: EP1387820B1
Принадлежит: BASF SE

Verfahren zur Herstellung einer gereinigten Schmelze einer durch Kondensation, Absorption oder Extraktion gewonnenen Monomerenschmelze in einem Kristallisator, wobei der Zulauf zum Kristallisator einer mechanischen fest/flüssig-Trennoperation unterworfen wird.

Подробнее
03-05-2022 дата публикации

Micro-channel permeation gasification device and method for synthesizing pyrrolidone alkali metal salt

Номер: CN114425239A
Автор: 储博钊, 王菊, 钟思青, 马俊

本发明公开了一种微通道渗透气化装置,包括一组或多组渗透气化组件单元;其中,每个所述渗透气化组件单元依次层叠的反应基板、渗透气化膜和气化基板。本发明还公开了用所述装置进行合成吡咯烷酮碱金属盐的方法。

Подробнее
22-01-1997 дата публикации

Process for the preparation of N-substituted pyrolidin-2-ones

Номер: EP0422366B1
Принадлежит: BASF SE

Подробнее
24-03-2004 дата публикации

Method for manufacturing n-alkyl-2-pyrrolidone

Номер: KR100404579B1
Автор: 곽병성, 김춘길, 윤영식
Принадлежит: 에스케이 주식회사

PURPOSE: Provided is a method for manufacturing N-alkyl-2-pyrrolidone by reacting alkylamines under mild reaction condition, thereby producing N-alkyl-2-pyrrolidone(NAP) stablely with high yield for a long time. CONSTITUTION: In a method for manufacturing N-alkyl-2-pyrrolidone by reacting a mixture of gammabutyrolactone(GBL), alkylamine and water in a catalyst reaction system, it is characterized in that the molar ratio of gammabutyrolactone:alkylamine:water is 1:(1-6):(1-18), its reaction temperature and pressure are 200-400 deg.C and 0-20kg/cm¬2G, respectively, it uses beta zeolite(MeNa beta) as a catalyst, and the space speed of reaction products is 0.1-20 hour¬-1.

Подробнее
09-04-2019 дата публикации

A kind of method of synthesis α, β unsaturated acyl amine compounds

Номер: CN106748949B
Принадлежит: XIAMEN UNIVERSITY

一种合成α,β不饱和酰胺化合物的方法,涉及α,β不饱和酰胺。提供一种以稳定易得的环状叔酰胺为原料,效率较高的一种合成α,β不饱和酰胺化合物的方法。将叔酰胺加入卤代烃溶剂中,与三氟甲烷磺酸酐、有机碱、芳醛进行缩合反应后,经萃取、干燥、浓缩、纯化后,即得α,β不饱和酰胺化合物。以稳定易得的环状叔酰胺为原料,高效率地合成一类α,β不饱和酰胺化合物;操作、分离简单,所用的试剂均为常用试剂,廉价易得。

Подробнее
12-07-2005 дата публикации

Production of 5-methyl-n-(methyl aryl)-2-pyrrolidone, 5-methyl-n-(methyl cycloalkyl)-2-pyrrolidone and 5-methyl-n-alkyl-2-pyrrolidone by reductive amination of levulinic acid esters with cyano compounds

Номер: US6916842B2
Автор: Leo Ernest Manzer
Принадлежит: EI Du Pont de Nemours and Co

This invention relates to a process for producing 5-methyl-N-(methyl aryl)-2-pyrrolidone, 5-methyl-N-(methyl cycloalkyl)-2-pyrrolidone and 5-methyl-N-alkyl-2-pyrrolidone by reductive amination of levulinic acid esters with aryl or alkyl cyano compounds utilizing a metal catalyst, which is optionally supported.

Подробнее
03-07-1991 дата публикации

Process for the preparation of vinyl derivatives

Номер: GB9110110D0
Автор: [UNK]

Подробнее
20-12-2007 дата публикации

Process for the alkenylation of carboxylic acid amides

Номер: DE102006028000A1
Принадлежит: BASF SE

Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung von N-(1-Alkenyl)-carbonsäureamiden der Formel I, wobei man ein Carbonsäureamid der Formel II mit einem Alkin der Formel III in Anwesenheit eines Katalysators, der ausgewählt ist unter Carbonylkomplexen, den Halogeniden oder Oxiden des Rheniums, Mangans, Wolframs, Molybdäns, Chroms und Eisens, umsetzt. The present invention relates to a process for the preparation of N- (1-alkenyl) -carboxamides of the formula I which comprises reacting a carboxamide of the formula II with an alkyne of the formula III in the presence of a catalyst selected from carbonyl complexes, the halides or oxides of rhenium, manganese, tungsten, molybdenum, chromium and iron.

Подробнее
13-05-1966 дата публикации

Nu-vinyl-pyrrolidone polymerization process

Номер: FR1438227A
Автор:
Принадлежит: General Aniline and Film Corp

Подробнее
24-11-2011 дата публикации

Processes for the production of pyrrolidones

Номер: CA2799376A1
Принадлежит: Bioamber SAS

Processes for making pyrrolidones include making MAS and/or SA from a clarified DAS- and/or MAS-containing fermentation broth and converting the MAS or SA to the pyrrolidones, typically with catalysts at selected temperatures and pressures.

Подробнее
16-05-2007 дата публикации

Process for the preparation of n-akyl-pyrrolidones

Номер: CN1964943A
Принадлежит: DAVID PROCESS TECHNOLOGY Ltd

一种由γ-丁内酯和单烷基胺在液相中制备N-烷基-吡咯烷酮的方法,该方法包括以下步骤:在无水情况下或水的存在量小于1wt%的情况下,将单烷基胺和γ-丁内酯进料到反应区以形成反应混合物;加热该反应混合物;从该反应区中回收产品流并使该产品流经过蒸馏区,所述蒸馏区包括至少一个在低于常压下工作的蒸馏塔;往蒸馏区中添加水;将至少一种塔顶流从该蒸馏区中分离,所述蒸馏区包括单烷基胺、水和任选的N-烷基-吡咯烷酮,并用冷却水冷凝该塔顶流。

Подробнее
02-06-1972 дата публикации

Pyrrolidinone-2 prepn - by low pressure hydrogenation of succinimide with supported palladium catalyst in aq medium

Номер: FR2111347A5
Автор: [UNK]
Принадлежит: Sunoco Inc

Pyrrolidin-zone is prepared by hydrogenation of succinimide with Pd catalyst on inert support (carbon) in aq. medium under H2 pressure >68 bars (pref. 82-105 bars) at 200-300 degrees C (pref. 225-275 degrees C). Catalyst contains 0.5-10wt.% Pd and is used in amount 5-20wt% of the succinimide. Reaction time is 1-5hr.

Подробнее
27-02-2013 дата публикации

Process for preparing of-butyrolactone and n-methyl pyrrolidone from 1,4-butanediol

Номер: CN102029156B

本发明提供在非铬催化剂的存在下由1,4-丁二醇制备γ-丁内酯(GBL)和由1,4-丁二醇制备N-甲基吡咯烷酮(NMP)的方法。更具体而言,本发明提供下述方法:所述方法在不含铬的非铬催化剂的存在下以环境友好的方式制备γ-丁内酯,所述制备具有很高的成本效益,长时间仅需要较低的成本,具有很高的产率和选择性,然后所述方法以高产率、长期稳定地制备N-甲基吡咯烷酮,该制备在温和的条件下不使用催化剂而通过将得到的γ-丁内酯和一甲胺(MMA)水溶液供应至反应器以使γ-丁内酯和一甲胺相互反应而进行。

Подробнее
04-03-1977 дата публикации

Patent FR2263239B1

Номер: FR2263239B1
Автор: [UNK]
Принадлежит: ILE DE FRANCE ETUDES SCIENTIFIQU

Подробнее
04-06-1976 дата публикации

PYRROLIDONS, THEIR PREPARATION PROCESS AND THEIR APPLICATIONS

Номер: FR2290199A1
Автор: [UNK]
Принадлежит: Hoechst AG

Подробнее
29-09-1978 дата публикации

PROCESS FOR RECOVERING 2-PYRROLIDONE FROM AQUEOUS ALKALINE SOLUTIONS

Номер: FR2382442A1
Автор: [UNK]

L'invention concerne les perfectionnements apportés à un procédé, catalysé par une substance alcaline, de production de poly-2-pyrrolidone. On traite la solution aqueuse alcaline contenant la poly-2-pyrrolidone de réaction par un acide pour obtenir un pH égal ou inférieur à 7. On récupère la pyrrolidone polymérisable à partir de la solution traitée par une évaporation en deux stades dont un sous pression réduite. La poly-2-pyrrolidone permet de produire des matières du type << Nylon >>. The invention relates to improvements in an alkaline-catalyzed process for the production of poly-2-pyrrolidone. The alkaline aqueous solution containing the reaction poly-2-pyrrolidone is treated with an acid to obtain a pH equal to or less than 7. The polymerizable pyrrolidone is recovered from the treated solution by evaporation in two stages, one of which is under reduced pressure. . Poly-2-pyrrolidone makes it possible to produce materials of the "nylon" type.

Подробнее
16-07-1965 дата публикации

Manufacturing process of dimethylacetamide

Номер: FR1406279A
Автор:
Принадлежит: EI Du Pont de Nemours and Co

Подробнее
19-03-1971 дата публикации

N-alkyllactams prodn

Номер: FR2048383A5
Автор: [UNK]
Принадлежит: Leuna Werke GmbH

N-alkyllactams (1-4C alkyl) are made by treating the corresponding unsubtsd. lactam (4-8C in the ring) with a sym. dialkyl ether (about 2-fold excess) with a water-splitting catalyst (esp. Al2O3) at 250-350 degrees C. Yields are around 65-75%.

Подробнее
19-06-1953 дата публикации

Process for the production of n-alkylated lactam

Номер: FR1031145A
Автор:
Принадлежит: Badische Anilin and Sodafabrik AG, BASF SE

Подробнее
18-08-1975 дата публикации

10-Aza prostaglandins - for treatment of blood pressure and gastro-intestinal disorders and in prepn for confinement

Номер: FR2258376A1
Автор: [UNK]
Принадлежит: ARIES ROBERT FR

10-Azaprostaglandins are of formula (I) (where R = H or lower alkyl; R' and R" = CH3 or C2H5; R degrees = H or lower alkyl; Y = -CH2-CH2-, or -CH=CH-; and Z = -CO or -CH.

Подробнее
30-08-1985 дата публикации

IMINO-2 PYRROLIDINES, THEIR PREPARATION PROCESS AND THEIR THERAPEUTIC APPLICATIONS

Номер: FR2540109B1
Автор: [UNK]
Принадлежит: Laboratoires Jacques Logeais SA

Подробнее
28-07-1978 дата публикации

Patent FR2290199B1

Номер: FR2290199B1
Автор: [UNK]
Принадлежит: Hoechst AG

Подробнее
13-01-2023 дата публикации

Process for obtaining biosourced N-vinylpyrrolidone monomer

Номер: FR3125046A1
Принадлежит: SNF SA

La présente invention concerne un procédé d’obtention d’un monomère N-Vinyl Pyrrolidone à partir de 2-Pyrrolidone ou d’Hydroxyéthyl Pyrrolidone, lesdits 2-Pyrrolydone et Hydroxyéthyl Pyrrolidone étant au moins en partie d’origine renouvelable et non fossile. L’invention concerne également un monomère N-vinylpyrrolidone biosourcé, un polymère biosourcé incorporant au moins ledit monomère, et l’utilisation dudit polymère dans différents domaines techniques. The present invention relates to a process for obtaining an N-Vinyl Pyrrolidone monomer from 2-Pyrrolidone or Hydroxyethyl Pyrrolidone, said 2-Pyrrolydone and Hydroxyethyl Pyrrolidone being at least partly of renewable and non-fossil origin. The invention also relates to a biobased N-vinylpyrrolidone monomer, a biobased polymer incorporating at least said monomer, and the use of said polymer in various technical fields.

Подробнее
02-01-1981 дата публикации

Patent FR2382471B1

Номер: FR2382471B1
Автор: [UNK]

Подробнее
26-03-1965 дата публикации

Process for preparing nu-vinylpyrrolidone

Номер: FR1393615A
Автор:
Принадлежит: INST ORGANIYCHESKOI KHIM IM N

Подробнее
03-09-1976 дата публикации

Patent FR2235685B1

Номер: FR2235685B1
Автор: [UNK]

Подробнее
20-05-1966 дата публикации

Process for the preparation of nu-substituted alpha-pyrrolidones

Номер: FR1439192A
Автор:

Подробнее
01-08-1980 дата публикации

METHOXY-2 BENZAMIDES AND THEIR THERAPEUTIC APPLICATION

Номер: FR2445829A2
Принадлежит: Synthelabo SA

Méthoxy-2 benzamides, sous forme de racémates ou d'énantiomères répondant à la formule I : 2-methoxy benzamides, in the form of racemates or enantiomers corresponding to formula I:

Подробнее