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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

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Мониторинг СМИ

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

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Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 170. Отображено 163.
11-02-2020 дата публикации

ПИПЕРИДИНИЛПИРАЗОЛОПИРИМИДИНОНЫ И ИХ ПРИМЕНЕНИЕ

Номер: RU2713937C2

FIELD: chemistry. SUBSTANCE: present invention relates to novel substituted piperidinylpyrazolopyrimidinones, having structural formula (I-A), in which radicals and symbols have the definitions given in the claim, methods for preparing them, based medicinal agents, use thereof in a method of treating and/or preventing diseases. EFFECT: compounds can be used for treating and/or preventing acute and recurrent haemorrhage in patients with underlying hereditary or acquired haemostatic disorders or without them, where haemorrhage is associated with a disease or medical intervention selected from a group including severe menstrual bleeding, postpartum haemorrhage, haemorrhoid shock, haemorrhagic cystitis, gastrointestinal bleeding, trauma, surgical intervention, transplantation, stroke, liver disease, hereditary angioedema, nosebleed and synovitis and cartilage damage following haemarthrosis. 18 cl, 4 tbl, 472 ex РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 713 937 C2 (51) МПК C07D 487/04 (2006.01) A61K 31/519 (2006.01) A61K 31/5377 (2006.01) A61K 31/541 (2006.01) A61K 45/06 (2006.01) A61P 7/04 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ ИЗОБРЕТЕНИЯ К ПАТЕНТУ (52) СПК C07D 487/04 (2019.05); A61K 31/519 (2019.05); A61K 31/5377 (2019.05); A61K 31/541 (2019.05); A61K 45/06 (2019.05); A61P 7/04 (2019.05) (21)(22) Заявка: 2017119419, 30.10.2015 30.10.2015 Дата регистрации: 11.02.2020 03.11.2014 EP 14191410.1; 30.04.2015 EP 15165918.2 (43) Дата публикации заявки: 05.12.2018 Бюл. № 34 (45) Опубликовано: 11.02.2020 Бюл. № 5 (86) Заявка PCT: EP 2015/075208 (30.10.2015) R U 2 7 1 3 9 3 7 (87) Публикация заявки PCT: WO 2016/071216 (12.05.2016) Адрес для переписки: 105064, Москва, а/я 88, "Патентные поверенные Квашнин, Сапельников и партнеры" (73) Патентообладатель(и): БАЙЕР ФАРМА АКЦИЕНГЕЗЕЛЬШАФТ (DE) (56) Список документов, цитированных в отчете о поиске: WO 2014/173289 A1, 30.10.2014. WO 2012/047156 A1, 12.04.2012. WO 2014/012964 A1, 23.01.2014. RU ...

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08-04-2010 дата публикации

1,4,2-Diazaphospholidin-Derivate

Номер: DE102008050414A1
Принадлежит:

Die vorliegende Erfindung betrifft neuartige 1,4,2-Diazaphospholidin-Derivate, ein Verfahren zu deren Herstellung sowie die Verwendung als Katalysatoren.

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26-07-1972 дата публикации

ACYLATION OF NITROGEN-CONTAINING PRODUCTS

Номер: GB0001282887A
Автор:
Принадлежит:

... 1282887 Polyolefin derivatives LUBRIZOL CORP 16 June 1969 [3 July 1968] 30409/69 Heading C3P [Also in Divisions C4-C5] Polyolefin derivatives suitable as dispersants for lubricating and fuel oils may be prepared by reacting (I) polyolefin substituted mono- or polycarboxylic acylating agents with (II) not more than one mole per equivalent of I of where R is an organic radical of valence n + 1 or, where n is 1, may be a direct linkage, and n is 1 to 3; X1 and X11 are independently O= or R 1 N=; when X1 is O = then Y is or where m is 0 or 1 to 8; when X1 is R 1 N= then R 1 is -(R11-NR1)m-R11-NR1R1 and Y is -NR1-(R11-NR1) m -R11-NR1R1 or R 1 and Y together form where q is 0 or 1 to 8; when X11 is O = then Z is O-M+, halo, alkoxy or Y as defined when X1 is O = and M+ is the cation of an amine; when X11 R 1 N = then ...

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27-08-1973 дата публикации

Procedure for the production of new Phenacetylguanidine and their acid addition salts

Номер: AT0000309461B
Автор:
Принадлежит: Wander Ag Dr A

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27-08-1973 дата публикации

Procedure for the production of new Phenacetylguanidine and their acid addition salts

Номер: AT0000309460B
Автор:
Принадлежит:

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02-08-2012 дата публикации

ARYLALKYL ESTERS OF 4-AMINO-6-(SUBSTITUTED PHENYL)PICOLINATES AND 6-AMINO-2-(SUBSTITUTED PHENYL)-4-PYRIMIDINECARBOXYLATES AND THEIR USE AS HERBICIDES

Номер: CA0002825878A1
Принадлежит:

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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31-08-1971 дата публикации

Guanidine derivs as antihypertensive agents

Номер: CH0000511815A
Принадлежит: WANDER AG DR A, DR. A. WANDER AG

Guanidine derivs. as antihypertensive agents Cpds. are (2-R1-6-R2-phenyl).ClH2CON=C(NR3R4)-(NR5R6) (where R1 is H, Cl or Me; R2 is Cl or Me; R3, R4, R5, R6 are the same or different and are H, alkyl, hydroxyalkyl or alkoxyalkyl of up to 6C, at least one being other than H, or R4 and R5 together are -(CH2)2- or -(CH2)3 and R3 and R6 are each H) and the salts thereof.

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31-05-1972 дата публикации

Guanidine derivs as antihypertensive agents

Номер: CH0000523231A
Принадлежит: WANDER AG DR A, DR. A. WANDER AG

Guanidine derivs. as antihypertensive agents Cpds. are (2-R1-6-R2-phenyl).ClH2CON=C(NR3R4)-(NR5R6) (where R1 is H, Cl or Me; R2 is Cl or Me; R3, R4, R5, R6 are the same or different and are H, alkyl, hydroxyalkyl or alkoxyalkyl of up to 6C, at least one being other than H, or R4 and R5 together are -(CH2)2- or -(CH2)3 and R3 and R6 are each H) and the salts thereof.

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27-03-1992 дата публикации

PROCESS FOR THE PREPARATION OF ALKYLIMIDAZOLIDONE (METH-) ACRYLATE COPOLYMERS.

Номер: FR0002655987B1
Принадлежит: Norsolor SA

A compound (I) is prepared by reacting at least one (meth)acrylate (II) with a heterocyclic alcohol (III) in the presence of at least one catalyst chosen from tin dialkyloxides and/or tin dialkyldialkoxides. <??>Alkylimidazolidone acrylates and methacrylates are known for the part they play in the constitution of polymers which are useful as coatings and adhesives and for paper and textile treatment, as well as for their use as leather treatment agents and in the production of emulsion paints. R1 = H, CH3; A,B = alkylene group with a straight or branched chain containing from 2 to 5 carbon atoms.

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07-06-1988 дата публикации

Process for the preparation of aryl-pyrido(1,4) benzodiazepines

Номер: US4749788A
Автор:
Принадлежит:

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27-10-2015 дата публикации

СЛОЖНЫЕ АРИЛАЛКИЛОВЫЕ ЭФИРЫ 4-АМИНО-6-(ЗАМЕЩЕННЫЙ ФЕНИЛ)ПИКОЛИНАТОВ И 6-АМИНО-2-(ЗАМЕЩЕННЫЙ ФЕНИЛ)-4-ПИРИМИДИНКАРБОКСИЛАТОВ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ГЕРБИЦИДОВ

Номер: RU2566760C2

FIELD: chemistry. SUBSTANCE: invention relates to novel arylalkyl esters of 4-aminopicolinic acids of formula IB, having herbicidal activity, and can be used for weed control. In formula IB: X is H or F; Y is phenyl, substituted with 1-4 substitutes independently selected from halogen, C 3 -C 6 cycloalkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy; Z is halogen; R 1 and R 2 is H; R 3 is an arylalkyl, selected from naphthyl-(C 1-2 )alkyl or phenyl-(C 1-2 )alkyl, which can be unsubstituted or substituted with 1-2 substitutes, independently selected from halogen, nitro, cyano, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, halogenated C 1 -C 6 alkyl, halogenated C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, C(O)OC 1 -C 6 alkyl, or where two adjacent substitutes taken together are -O(CH 2 ) n O- or -O(CH 2 ) n -, where n=1 or 2. EFFECT: compounds have selective action and are particularly applicable, at the post-germination phase, to control types which are usually encountered in systems for growing rice, wheat or fodder plants. 9 cl, 28 tbl, 17 ex РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 566 760 C2 (51) МПК C07D 239/42 (2006.01) C07D 239/30 (2006.01) A01N 43/54 (2006.01) A01P 13/00 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ (21)(22) Заявка: ИЗОБРЕТЕНИЯ К ПАТЕНТУ 2013139370/04, 24.01.2012 (24) Дата начала отсчета срока действия патента: 24.01.2012 Приоритет(ы): (30) Конвенционный приоритет: (43) Дата публикации заявки: 10.03.2015 Бюл. № 7 (73) Патентообладатель(и): ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи (US) (56) Список документов, цитированных в отчете о поиске: EP 2191720 A1, 02.06.2010. WO 2010125332 A1, 04.11.2010. WO 2010092339 A1,19.08.2010. WO 2007120706 A2, 25.10.2007. WO 2005063721 A1, 14.07.2005 . WO 2008073369 A1, 19.06.2008 . WO 2007092184 A2, 16.08.2007. WO 2006121648 A2,16.11.2006. US 2009048109 A1, 19.02.2009 . US 3325272 A, 13. 06.1967. US 6297197 B1,02.10.2001. US 3285925 A, 15. 11.1966. US 2009088322 A1,02.04.2009. US 2010041556 A1,18.02. ...

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22-07-2021 дата публикации

(Е)-(6-(2-гидроксифенил)-2-иминио-4,7,8-триоксо-1,3-дифенил-1,3,6-триазаспиро[4.4]нонан-9-илиден)(4-метоксифенил)метаноат, обладающий противомикробной активностью, и способ его получения

Номер: RU2752079C1

FIELD: organic chemistry. SUBSTANCE: invention relates to the field of organic chemistry, namely to a new individual compound (E)-(6-(2-hydroxyphenyl)-2-iminio-4,7,8-trioxo-1,3-diphenyl-1,3,6-triazaspiro [4.4] nonan-9-ylidene) (4-methoxyphenyl)methanoate and its preparation method. EFFECT: technical result is preparation of an individual compound (E)-(6-(2-hydroxyphenyl)-2-iminio-4,7,8-trioxo-1,3-diphenyl-1,3,6-triazaspiro [4.4] nonan-9-ylidene) (4-methoxyphenyl)methanoate, which has antimicrobial activity, and the development of a simple method of its production, which can be used as a starting product for the synthesis of new heterocyclic systems and in pharmacology. 2 cl, 1 tbl, 2 ex РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 752 079 C1 (51) МПК C07D 247/02 (2006.01) A61K 31/4162 (2006.01) A61P 31/04 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ ИЗОБРЕТЕНИЯ К ПАТЕНТУ (52) СПК C07D 247/02 (2021.02); A61K 31/4162 (2021.02); A61P 31/04 (2021.02) (21)(22) Заявка: 2020139576, 01.12.2020 (24) Дата начала отсчета срока действия патента: Дата регистрации: 22.07.2021 (45) Опубликовано: 22.07.2021 Бюл. № 21 2 7 5 2 0 7 9 R U (56) Список документов, цитированных в отчете о поиске: RU 2707195 C1, 25.11.2019. RU 2631432 C1, 22.09.2017. RU 2269528 C2, 10.02.2006. WO 2017/214367, 14.12.2017. Krolenko, K.Y., Silin, O.V., Vlasov, S.V. et al. An Efficient Synthesis of 1,3,7-Triazaspiro[4.4]Nonane-2,4Dione Derivatives and Antimicrobial Activity Thereof. Chem Heterocycl Comp 51, 472-477 (2015). (54) (Е)-(6-(2-гидроксифенил)-2-иминио-4,7,8-триоксо-1,3-дифенил-1,3,6-триазаспиро[4.4]нонан-9-илиден)(4метоксифенил)метаноат, обладающий противомикробной активностью, и способ его получения (57) Реферат: Изобретение относится к области гидроксифенил)-2-иминио-4,7,8-триоксо-1,3органической химии, а именно к новому дифенил-1,3,6-триазаспиро [4.4] нонан-9-илиден) индивидуальному соединению (Е)-(6-(2(4-метоксифенил)метаноата, обладающего гидроксифенил)-2-иминио-4,7,8 ...

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10-06-2019 дата публикации

Patent RU2017119419A3

Номер: RU2017119419A3
Автор: [UNK]
Принадлежит: [UNK]

ВУ” 2017119419`” АЗ Дата публикации: 10.06.2019 Форма № 18 ИЗПМ-2011 Федеральная служба по интеллектуальной собственности Федеральное государственное бюджетное учреждение 5 «Федеральный институт промышленной собственности» (ФИПС) ОТЧЕТ О ПОИСКЕ 1. . ИДЕНТИФИКАЦИЯ ЗАЯВКИ Регистрационный номер Дата подачи 2017119419/04(033710) 30.10.2015 РСТ/ЕР2015/075208 30.10.2015 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. 14191410.1 03.11.2014 ЕР* 2. 15165918.2 30.04.2015 ЕР* Название изобретения (полезной модели): [Х] - как заявлено; [ ] - уточненное (см. Примечания) ПИПЕРИДИНИЛПИРАЗОЛОПИРИМИДИНОНЫ И ИХ ПРИМЕНЕНИЕ Заявитель: БАЙЕР ФАРМА АКЦИЕНГЕЗЕЛЬШАФТ, 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) (070 487/04 (2006.01) Аб1К 31/5377 (2006.01) Аб1К 45/06 (2006.01) Аб1К 31/519 (2006.01) Аб1К 31/541 (2006.01) Аб1Р 7/04 (2006.01) 5. ОБЛАСТЬ ПОИСКА 5.1 Проверенный минимум документации РСТ (указывается индексами МПК) С07О 487/04, Аб1К 31/519, Аб1К 31/5377, Аб1К 31/541, Аб1К 45/06, Аб1Р 7/04 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, Езрасепек, ]-Р]1а Ра, РАТЕМТЗСОРЕ, Рабеагсв ...

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10-03-2015 дата публикации

СЛОЖНЫЕ АРИЛАЛКИЛОВЫЕ ЭФИРЫ 4-АМИНО-6-(ЗАМЕЩЕННЫЙ ФЕНИЛ)ПИКОЛИНАТОВ И 6-АМИНО-2-(ЗАМЕЩЕННЫЙ ФЕНИЛ)-4-ПИРИМИДИНКАРБОКСИЛАТОВ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ГЕРБИЦИДОВ

Номер: RU2013139370A
Принадлежит:

... 1. Соединение формулы IA:где Y представляет собой C-Cалкил, C-Cциклоалкил или фенил, замещенный 1-4 заместителями, независимо выбранными из галогена, C-Cалкила, C-Cциклоалкила, C-Cалкокси, C-Cгалогеналкила, C-Cгалогеналкокси, циано, нитро, NRR, или где два смежных заместителя, взятые вместе, представляют собой -O(CH)O- или -O(CH)-, где n=1 или 2;Z представляет собой галоген, C-Cалкокси или C-Cалкенил;Rи Rнезависимо представляют собой H, C-Cалкил, C-Cалкенил, C-Cалкинил, гидрокси, C-Cалкокси, амино или C-Cацил;Rпредставляет собой незамещенный или замещенный C-Cарилалкил.2. Соединение по п.1, где Y представляет собой замещенный фенил.3. Соединение по п.1, где Z представляет собой Cl, -CH=CHили OCH.4. Соединение по п.1, где Rи Rпредставляют собой H.5. Соединение по п.1, где Rпредставляет собой бензил.6. Соединение по п.1, где Rпредставляет собой незамещенный или орто-, мета- или пара-монозамещенный бензил.7. Соединение формулы IB:где X представляет собой H или F;Y представляет собой галоген ...

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15-03-1995 дата публикации

PROCEDURE FOR THE PRODUCTION OF ALKYLIMIDAZOLIDONE (METH) ACRYLATE.

Номер: AT0000118486T
Принадлежит:

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12-05-2016 дата публикации

PIPERIDINYLPYRAZOLOPYRIMIDINONES AND THEIR USE

Номер: CA0002966259A1
Принадлежит:

The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

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12-08-2014 дата публикации

Non-metal tanning process

Номер: US0008801804B2
Принадлежит: Stahl International B.V.

Tanned leather, skin or pelt is produced by non-metal tanning, comprising the step of tanning a bated hide, skin or belt with a tanning agent (A) of at least a mixture of compounds of formula (I) and formula (II), wherein Hal signifies fluorine or chlorine, R1 signifies hydrogen, C 1-8 -alkyl or an alkyleneoxy radical of formula (III), —(—C 2-3 alkylene-O—) q —H (III); R2 signifies a) phenyl, mono- or di-substituted with SO 3 M or COOM and optionally substituted also with hydroxyl, C 1-4 -alkyl C 1-4 -alkoxy; b) naphthyl, mono- or di- or tri-substituted with SO 3 M and optionally substituted also with hydroxyl; c) C 1-8 -alkylene, substituted with (SO 3 M) or (COOM); d) aradical of formula (IV), —(—C 2-3 alkylene-O—) p —Y (IV) or e) a radical of formula (IVa) —(C 2-3 alkylene-O) p —C 2-3 alkylene-SO 2 CH2CH 2 O—Y (IVa), M signifies 1 or 2, p signifies 0 or 1, Y signifies hydrogen or —SO 3 M, q signifies 1 to 10, M signifies hydrogen, an alkali metal cation or an ammonium cation being aprotonated tertiary amine or a quaternary ammonium cation, R3 signifies hydrogen or chlorine. In a tanning bath having a pH of from 6 to 10 at the beginning of tanning step.

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11-05-1993 дата публикации

PROCESS FOR THE PREPARATION OF ALKYLIMIDAZOLIDONE (METH) ACRYLATE

Номер: US0005210199A
Автор:
Принадлежит:

At least one (meth)acrylate is reacted with a heterocyclic alcohol (III) in the presence of at least one catalyst chosen from dialkyltin oxides and dialkyltin dialkoxides. Alkylimidazolidone acrylates and methacrylates are known for the part they play in the constitution of polymers which can be used as coatings and adhesives and for the treatment of paper and textiles, and for their use as agents for the treatment of leather and in the production of emulsion paints. (I) (II) (III) R1=H, CH3 ; A, B=straight or branched chain alkylene group containing from 2 to 5 carbon atoms.

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01-12-1982 дата публикации

1,3-DIARY-2-IMINO-IMIDAZOLIDINES OR HEXAHYDROPYRIMIDES

Номер: GB0002022577B
Автор:

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27-08-1973 дата публикации

Procedure for the production of new hetero-cyclic connections and their acid addition salts

Номер: AT0000309415B
Автор:
Принадлежит: Wander Ag Dr A

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16-04-2015 дата публикации

Arylalkyl esters of 4-amino-6-(substituted phenyl)picolinates and 6-amino-2-(substituted phenyl)-4-pyrimidinecarboxylates and their use as herbicides

Номер: AU2012209278B2
Принадлежит: CORTEVA AGRISCIENCE LLC

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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27-07-1999 дата публикации

PROCESS FOR THE PREPARATION OF ALKYL IMIDAZOLIDONE (METH)ACRYLATE

Номер: CA0002032355C
Принадлежит: Atochem SA

On prépare un composé (I) en faisant réagir au moins un (méth)acrylate (II) avec un alcool hétérocyclique (III), en présence d'au moins un catalyseur choisi parmi les dialkyloxydes d'étain, les dialkyldialcoxydes d'étain. Les acrylates et méthacrylates d'alkylimidazolidone sont connus pour leur rôle dans la constitution de polymères utiles comme revêtements et adhésifs, et pour le traitement du papier et des textiles, ainsi que pour leur utilisation comme agents de traitement du cuir et dans la production de peintures en émulsion.

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16-11-1979 дата публикации

NEWS 1,3-DIARYL-2-IMINO-IMIDAZOLIDINES AND 1,3-DIARYL-2-IMINO-HEXAHYDRO-PYRIMIDINES SUBSTITUEES, METHODS OF PREPARATION OF THESE COMPOSE AND DRUGS the CONTAINER

Номер: FR0002423485A1
Принадлежит: Egyt Gyogyszervegyeszeti Gyar

Nouvelles 1,3-diaryl-2-imino-imidazolidines et 1,3-diaryl 2-imino-hexahydro-pyrimidines substituées qui correspondent à la formule générale ci-après : New substituted 1,3-diaryl-2-imino-imidazolidines and 1,3-diaryl 2-imino-hexahydro-pyrimidines which correspond to the general formula below:

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26-03-2024 дата публикации

Or relating to curing agents

Номер: US0011939421B2
Принадлежит: HEXCEL COMPOSITES LIMITED

A curative system comprising a combination of adipic acid dihydrazide and/or isophthalic dihydrazide and a clathrate in which the guest compound of the clathrate comprises an imidazole, an imidazoline or diazabicycloalkanes (DBCA).

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12-12-1974 дата публикации

DIALCOHOL DERIVATIVES OF N-HETEROCYCLIC COMPOUNDS

Номер: AU0000456198B2
Автор:
Принадлежит:

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11-09-2018 дата публикации

ARYLALKYL ESTERS OF 4-AMINO-6-(SUBSTITUTED PHENYL)PICOLINATES AND ITS USE AS HERBICIDES

Номер: CA0002925262C
Принадлежит: DOW AGROSCIENCES LLC

The invention relates to a compound of Formula (IA): (see formula (IA) wherein: Y represents C1-C8 alkyl, C3-C6 cycloalkyl, or phenyl substituted with 1-4 substituents independently selected from the group consisting of halo, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy, cyano, nitro and NR1R2, or where two adjacent substituents are taken together as ~O(CH2)n O~ or ~O(CH2)n~, wherein n=1 or 2; Z represents halo, C1-C3 alkoxy, or C2-C4 alkenyl; R1 and R2 independently represent H, C1-C6 alkyl, C3-C6 alkenyl, C3-C6 alkynyl, hydroxy, C1-C6 alkoxy, amino, or C1-C6 acyl; and R3 represents unsubstituted or substituted C7-C11 arylalkyl.

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13-03-1970 дата публикации

ACYLATION OF NITROGEN-CONTAINING PRODUCTS

Номер: FR0002012253A1
Автор:
Принадлежит:

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21-06-1991 дата публикации

METHOD OF PREPARATION OF (METH) ACRYLATE Of ALKYLIMIDAZOLIDONE.

Номер: FR0002655987A1
Принадлежит:

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13-06-2019 дата публикации

PROCESS FOR THE PREPARATION OF BREXPIPRAZOLE AND INTERMEDIATES THEREOF

Номер: US20190177309A1
Принадлежит: CADILA HEALTHCARE LIMITED

The present invention relates to Brexpiprazole having a purity of about 99.5% or more by area percentage of HPLC, having total impurities not more than 0.5% relative to brexpiprazole as measured by area percentage of HPLC, and having less than 0.1% 1-(benzo[b]thiophen-4-yl)piperazine or a salt thereof relative to brexpiprazole by area percentage of HPLC. The present invention also provides a composition comprising brexpiprazole having 1-(benzo[b]thiophen-4-yl)-piperazine or a salt thereof in an amount less than about 0.1% relative to brexpiprazole by area percentage of HPLC and process for the preparation of brexpiprazole. 1. Brexpiprazole having a purity of about 99.5% or more by area percentage of HPLC.2. Brexpiprazole having total impurities not more than 0.5% relative to brexpiprazole as measured by area percentage of HPLC.3. Brexpiprazole having less than 0.1% 1-(benzo[b]thiophen-4-yl)piperazine or a salt thereof relative to brexpiprazole by area percentage of HPLC.4. Brexpiprazole according to which is substantially free from one or more of 7-(4-(4-(benzo[b]thiophen-4-yl)piperazin-1-yl)butoxy)-1-(4-(4-(benzo[b] thiophen-4-yl)piperazin-1-yl)butyl)quinolin-2(1H)-one (impurity-S); 2 claim 1 ,7-bis(4-(4-(benzo[b]thiophen-4-yl)piperazin-1-yl)butoxy)quinoline (impurity-T); or 7-(4-(4-(benzo[b]thiophen-4-yl)piperazin-1-yl)butoxy)-1 claim 1 ,2-dihydroquinoline (impurity-U) claim 1 , relative to brexpiprazole by area percentage of HPLC.5. The brexpiprazole according to which is crystallized from toluene.6. The brexpiprazole according to which is substantially free from residual solvents.7. The brexpiprazole according to comprising crystallizing brexpiprazole in one or more solvents.8. The brexpiprazole according to wherein the solvent comprises one or more of water claim 7 , methanol claim 7 , ethanol claim 7 , isopropanol claim 7 , butanol claim 7 , acetone claim 7 , methyl ethyl ketone claim 7 , methyl isobutylketone claim 7 , ethyl acetate claim 7 , isopropyl ...

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22-10-1992 дата публикации

VERFAHREN ZUR HERSTELLUNG VON N,N'-DIALKYLSUBSTITUIERTEN CYCLISCHEN HARNSTOFFDERIVATEN.

Номер: DE0003874715D1
Принадлежит: BASF AG, BASF AG, 6700 LUDWIGSHAFEN, DE

The prepn. of 1,3-dialkyl-2-imidazolidinone derivs. of formula (I) comprises reacting a diamine of formula (II) with carbon dioxide in the gas phase in the presence of oxides of elements of the 3rd or 4th main group or 2nd-6th subsidiary group of the periodic table, or mixts. of these or in the presence of aluminium or magnesium silicates. In the formulae, R1 and R2 = 1-8C alkyl; R3-R6 = H or 1-17C alkyl. 1, 3, 4-trimethyl-2-imidazolidinone (Ia) is new.

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24-03-2016 дата публикации

Non-metal tanning process

Номер: AU2011323043B2
Принадлежит:

Tanned leather, skin or pelt is produced by non-metal tanning, comprising the step of tanning a bated hide, skin or pelt with a tanning agent (A), the tanning agent (A) being at least a mixture of compounds of formula (I) and formula (II), wherein Hal signifies fluorine or chlorine, R1 signifies hydrogen, C ...

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30-07-1974 дата публикации

ACETYL GUANIDINE DERIVATIVES

Номер: CA952111A
Принадлежит: Wander AG

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16-06-1991 дата публикации

PROCESS FOR THE PREPARATION OF ALKYL IMIDAZOLIDONE (METH)ACRYLATE

Номер: CA0002032355A1
Принадлежит: Atochem, Didier Vanhoye, Paul Grosius

On prépare un composé (I) en faisant réagir au moins un (méth)acrylate (II) avec un alcool hétérocyclique (III), en présence d'au moins un catalyseur choisi parmi les dialkyloxydes d'étain, les dialkyldialcoxydes d'étain. Les acrylates et méthacrylates d'alkylimidazolidone sont connus pour leur rôle dans la constitution de polymères utiles comme revêtements et adhésifs, et pour le traitement du papier et des textiles, ainsi que pour leur utilisation comme agents de traitement du cuir et dans la production de peintures en émulsion. R1 = H, CH3; A, B = groupe alkylène à chaîne droite ou ramifiée ayant de 2 à 5 atomes de carbone. A compound (I) is prepared by reacting at least one (meth) acrylate (II) with a heterocyclic alcohol (III), in the presence of at minus one catalyst chosen from tin dialkyloxides, tin dialkyldialcoxides. Alkylimidazolidone acrylates and methacrylates are known for their role in the constitution of useful polymers like coatings and adhesives, and for the treatment of paper and textiles, as well as for their use as leather treatment agents and in the production of emulsion paints. R1 = H, CH3; A, B = straight or branched chain alkylene group having from 2 to 5 carbon atoms.

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11-12-1970 дата публикации

PHENYLACETYLGUANIDINES

Номер: FR0002034557A1
Автор: BREAM J, PICARD C
Принадлежит: Wander AG

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05-12-2018 дата публикации

ПИПЕРИДИНИЛПИРАЗОЛОПИРИМИДИНОНЫ И ИХ ПРИМЕНЕНИЕ

Номер: RU2017119419A

РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2017 119 419 A (51) МПК C07D 487/04 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ЗАЯВКА НА ИЗОБРЕТЕНИЕ (21)(22) Заявка: 2017119419, 30.10.2015 (71) Заявитель(и): БАЙЕР ФАРМА АКЦИЕНГЕЗЕЛЬШАФТ (DE) Приоритет(ы): (30) Конвенционный приоритет: 03.11.2014 EP 14191410.1; 30.04.2015 EP 15165918.2 34 (85) Дата начала рассмотрения заявки PCT на национальной фазе: 05.06.2017 EP 2015/075208 (30.10.2015) (87) Публикация заявки PCT: R U Адрес для переписки: 105064, Москва, а/я 88, ООО "Патентные поверенные Квашнин, Сапельников и партнеры" (54) ПИПЕРИДИНИЛПИРАЗОЛОПИРИМИДИНОНЫ И ИХ ПРИМЕНЕНИЕ (57) Формула изобретения 1. Соединение формулы (I-A) , в которой R1 выбран из водорода и C1-C5 алкила; R2 выбран из водорода, C1-C4 алкила, C1-C6 циклоалкила, C1-C4 галоалкила, карбоксила, C1-C4 алкилового сложного эфира, C1-C4 алкокси- C1-C4 алкила, галогена, метилсульфанила, фенила, Стр.: 1 A 2 0 1 7 1 1 9 4 1 9 A WO 2016/071216 (12.05.2016) 2 0 1 7 1 1 9 4 1 9 (86) Заявка PCT: R U (43) Дата публикации заявки: 05.12.2018 Бюл. № (72) Автор(ы): ЭЛЛЕРМАНН Мануэль (DE), ФАЛОТ Гелле (DE), КАНХО ГРАНДЕ Иоланда (DE), ХАССФЕЛЬД Йорма (DE), КИНЦЕЛЬ Том (CN), КЁББЕРЛИНГ Йоханнес (DE), БАЙЕР Кристин (DE), РЁРИГ Зузанне (DE), ШПЕРЦЕЛЬ Михаэль (DE), ШТАМПФУСС Ян (DE), МАЙЕР Имке (DE), КЁЛЛЬНБЕРГЕР Мариа (DE), БУРКХАРДТ Нильс (DE), ШЛЕММЕР Карл-Хайнц (DE), ШТЕГМАНН Кристиан (DE), ШУМАХЕР Йоахим (DE), ВЕРНЕР Маттиас (DE), ХАЙЕРМАНН Йорг (DE), ХЕНГЕВЕЛЬД Виллем Ян (NL) 2 0 1 7 1 1 9 4 1 9 R U A Стр.: 2 2 0 1 7 1 1 9 4 1 9 R3 выбран из водорода, галогена, циано, C1-C4 алкила, причем алкил необязательно замещен ди- C1-C4 алкиламино, C1-C4 алкенила, C1-C4 алкилового сложного эфира, причем C1-C4 алкиловый сложный эфир необязательно замещен одним, двумя, тремя, четырьмя или пятью заместителями галоген, C3-C4 циклоалкилового сложного эфира, C3-C4 циклоалкила, карбоксила, карбоксамида, бензилового сложного эфира, -NH-COфенила, -CS-NH2, фенилсульфонила ...

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13-10-1981 дата публикации

SUBSTITUTED 1,3-DIARYL-2-IMINO-IMIDAZOLIDINES AND 2- IMINO-HEXAHYDRO-PYRIMIDINES AND A PROCESS FOR THE PREPARATION THEREOF

Номер: CA1110626A
Принадлежит: EGYT GYOGYSZERVEGYESZETI GYAR

ABSTRACT OF THE DISCLOSURE The invention relates to new compounds of the general formula (I),

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02-08-2012 дата публикации

ARYLALKYL ESTERS OF 4-AMINO-6-(SUBSTITUTED PHENYL)PICOLINATES AND ITS USE AS HERBICIDES

Номер: CA0002925262A1
Принадлежит: DOW AGROSCIENCES LLC

The invention relates to a compound of Formula (IA): (see formula (IA) wherein: Y represents C1-C8 alkyl, C3-C6 cycloalkyl, or phenyl substituted with 1-4 substituents independently selected from the group consisting of halo, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy, cyano, nitro and NR1R2, or where two adjacent substituents are taken together as ~O(CH2)n O~ or ~O(CH2)n~, wherein n=1 or 2; Z represents halo, C1-C3 alkoxy, or C2-C4 alkenyl; R1 and R2 independently represent H, C1-C6 alkyl, C3-C6 alkenyl, C3-C6 alkynyl, hydroxy, C1-C6 alkoxy, amino, or C1-C6 acyl; and R3 represents unsubstituted or substituted C7-C11 arylalkyl.

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30-07-1974 дата публикации

ACETYL GUANIDINE DERIVATIVES

Номер: CA0000952111A1
Принадлежит:

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21-12-1973 дата публикации

PHENYLACETYLGUANIDINES

Номер: FR0002034557B1
Автор: C Picard, J Bream
Принадлежит: Wander AG

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18-10-2016 дата публикации

ARYLALKYL ESTERS OF 4-AMINO-6-(SUBSTITUTED PHENYL)PICOLINATES AND ITS USE AS HERBICIDES

Номер: CA0002825878C
Принадлежит: DOW AGROSCIENCES LLC

The invention relates to a compound of Formula (IB): (See Formula IB) wherein: X represents H or F; Y represents C1-C8 alkyl, C3-C6 cycloalkyl, or phenyl substituted with 1-4 substituents independently selected from the group consisting of halo, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy, cyano, nitro and NR1R2; Z represents CI or C2-C4 alkenyl; R1 and R2 independently represent H, C1-C6 alkyl, or C1-C6 acyl; and R3 represents unsubstituted or substituted C7-C11 arylalkyl. The compound may be useful as a herbicide for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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24-12-1997 дата публикации

Номер: JP0002695220B2
Автор:
Принадлежит:

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29-11-1972 дата публикации

PHENYL ACETYL GUANIDINE DERIVATIVES

Номер: GB0001298112A
Принадлежит:

... 1298112 Phenylacetylguanidine derivatives DR A WANDER SA 4 Feb 1970 [20 Feb 1969 27 March 1969 7 Nov 1969] 5422/70 Heading C2C The invention comprises compounds of formula and their acid addition salts, wherein R 1 is H, Cl or Me, R 2 is Cl or Me, and either (a) R 3 , R 4 , R 5 , R 6 are each (up to C 6 ) alkyl, hydroxyalkyl or alkoxyalkyl, or up to 3 of them may be H, or (b) R 4 -R 5 is CH 2 CH 2 or CH 2 CH 2 CH 2 , and R 3 , R 6 are each H. These compounds are prepared by (1) reacting 2,6-R 1 R 2 C 6 H 3 CH 2 CO 2 H or a reactive derivative thereof with (2) (for compounds (a)) reacting (where R is a reactive group capable of being split off) with R 5 R 6 NH, (3) (for compounds (b)) (i) reducing the corresponding phenylacetylamino-imidazole or -pyrimidine, or (ii) reacting II with (CH 2 ) 2-3 (NH 2 ) 2 . Starting material.- is prepared from 2,6-Cl 2 C 6 H 3 CH 2 COCl and HN= C(SMe)NH 2 . Therapeutic compositions for the treatment of hypertonia by oral or parenteral administration, comprise ...

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11-10-1973 дата публикации

DIALCOHOL DERIVATIVES OF N-HETEROCYCLIC COMPOUNDS

Номер: AU0005853573A
Принадлежит:

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16-11-1979 дата публикации

NOUVELLES 1,3-DIARYL-2-IMINO-IMIDAZOLIDINES ET 1,3-DIARYL-2-IMINO-HEXAHYDRO-PYRIMIDINES SUBSTITUEES, PROCEDES DE PREPARATION DE CES COMPOSES ET MEDICAMENTS LES CONTENANT

Номер: FR0002423485A
Принадлежит:

Nouvelles 1,3-diaryl-2-imino-imidazolidines et 1,3-diaryl 2-imino-hexahydro-pyrimidines substituées qui correspondent à la formule générale ci-après : ...

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09-06-1995 дата публикации

CATALYTIC TRANSESTERIFICATION PROCESS FOR THE PREPARATION OF (METH-) ACRYLIC.

Номер: FR0002700769B1
Принадлежит: Roehm GmbH Darmstadt

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21-06-1991 дата публикации

Procédé de préparation de (méth)acrylate d'alkylimidazolidone.

Номер: FR0002655987A
Принадлежит:

On prépare un composé (I) en faisant réagir au moins un (méth)acrylate (II) avec un alcool hétérocyclique (III), en présence d'au moins un catalyseur choisi parmi les dialkyloxydes d'étain, les dialkyldialcoxydes d'étain. Les acrylates et méthacrylates d'alkylimidazolidone sont connus pour leur rôle dans la constitution de polymères utiles comme revêtements et adhésifs, et pour le traitement du papier et des textiles, ainsi que pour leur utilisation comme agents de traitement du cuir et dans la production de peintures en émulsion. (CF DESSIN DANS BOPI) (CF DESSIN DANS BOPI) R1 = H, CH3 ; A, B = groupe alkylène à chaîne droite ou ramifiée ayant de 2 à 5 atomes de carbone.

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29-07-1994 дата публикации

Catalytic process of cross esterification for the preparation of esters of acid (méth) acrylic

Номер: FR0002700769A1
Принадлежит: Roehm GmbH Darmstadt

Il est décrit un procédé catalytique de préparation d'esters d'acide (méth)acrylique de formule I (CF DESSIN DANS BOPI) où R1 = H ou CH3 et où A et B = groupements alkylène non ramifiés ou ramifiés à 2-5 atomes de carbone, par réaction d'esters d'acide (méth)acrylique de formule II (CF DESSIN DANS BOPI) où R2 = reste alkyle à 1-4 atomes de carbone en particulier, et d'alcools de formule III (CF DESSIN DANS BOPI) en présence d'un composé de plomb servant de catalyseur. Après la réaction, le catalyseur est séparé du mélange réactionnel par filtration. There is described a catalytic process for the preparation of (meth) acrylic acid esters of formula I (CF DRAWING IN BOPI) where R1 = H or CH3 and where A and B = unbranched or branched alkylene groups with 2-5 atoms of carbon, by reaction of (meth) acrylic acid esters of formula II (CF DRAWING IN BOPI) where R2 = alkyl residue with 1-4 carbon atoms in particular, and alcohols of formula III (CF DRAWING IN BOPI) BOPI) in the presence of a lead compound serving as a catalyst. After the reaction, the catalyst is separated from the reaction mixture by filtration.

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23-10-2017 дата публикации

비-금속 태닝 방법

Номер: KR0101789042B1
Принадлежит: 스탈 인터내셔날 비.브이.

... 연화된 하이드, 스킨 또는 펠트를 태닝 단계의 초기에 pH가 6 내지 10인 태닝 욕에서 적어도 화학식 I의 화합물과 화학식 II의 화합물의 혼합물인 태닝제(A)로 태닝하는 단계를 포함하여, 비-금속 태닝에 의해, 태닝된 가죽, 스킨 또는 펠트가 생성된다.화학식 I 화학식 II 상기 화학식 I 및 II에서, Hal은 불소 또는 염소이고, R1은 수소, C1-8-알킬 또는 화학식 III의 알킬렌옥시 라디칼이고, R2는 a) SO3M 또는 COOM으로 일- 또는 이-치환되고 임의로 하이드록실 또는 C1-4-알킬 또는 C1-4-알콕시로 또한 치환되는 페닐이거나, 또는 b) SO3M으로 일- 또는 이- 또는 삼-치환되고 임의로 하이드록실로 또한 치환되는 나프틸이거나, 또는 c) (SO3M) 또는 (COOM)으로 치환되는 C1-8-알킬렌이거나, 또는 d) 화학식 IV의 라디칼이거나, 또는 e) 화학식 IVa의 라디칼이고,R3은 수소 또는 염소이다.화학식 III 화학식 IV 화학식 IVa 상기 화학식 III, IV 및 IVa에서,p는 0 또는 1이고, Y는 수소 또는 -SO3M이고, q는 1 내지 10이고, M은 수소 또는 알칼리 금속 양이온 또는 암모늄 양이온이고, 상기 암모늄 양이온은 양성자화된 3급 아민 또는 4급 암모늄 양이온이다.

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20-05-2014 дата публикации

1,4,2-diazaphospholidine derivatives

Номер: US0008729304B2

The present invention relates to a 1,4,2-diazaphospholidine of the formula (1) wherein R1, R2 represent, independently of one another, saturated or mono- or polyunsaturated C1-C20-alkyl, -alkenyl, -alkynyl or C5-C40-aryl groups optionally substituted or interrupted by at least one heteroatom selected from the group consisting of N, O, S, and halogen, and X represents identical or different substituents selected from the group consisting of O, S, and NR2.

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27-02-2020 дата публикации

Piperidinylpyrazolopyrimidinones and their use

Номер: AU2015342021B2
Принадлежит: Davies Collison Cave Pty Ltd

The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

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09-01-1973 дата публикации

PROCESS FOR THE MANUFACTURE OF NEW FENACETIL-GUANIDIMAS

Номер: BR0007016868D0
Автор: BREAM J, PICARD C
Принадлежит: Wander Ag Dr A

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01-03-2013 дата публикации

Arylalkyl esters of 4-amino-6-(substituted phenyl)picolinates and 6-amino-2-(substituted phenyl)-4-pyrimidinecarboxylates and their use as herbicides

Номер: TW0201309646A
Принадлежит:

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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04-09-2013 дата публикации

NON-METAL TANNING PROCESS

Номер: EP2633087A1
Принадлежит:

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25-10-2012 дата публикации

Non-metal tanning process

Номер: AU2011323043A1
Принадлежит:

Tanned leather, skin or pelt is produced by non-metal tanning, comprising the step of tanning a bated hide, skin or pelt with a tanning agent (A), the tanning agent (A) being at least a mixture of compounds of formula (I) and formula (II), wherein Hal signifies fluorine or chlorine, R1 signifies hydrogen, C-alkyl or an alkyleneoxy radical of formula (III), - (- C alkylene - O -) - H (III) R2 signifies a) phenyl, mono- or di-substituted with SOM or COOM and optionally substituted also with hydroxyl or C-alkyl or Calkoxy, or b) naphthyl, mono- or di- or tri-substituted with SOM and optionally substituted also with hydroxyl, or c) C-alkylene, substituted with (S0M) or (COOM), or d) a radical of formula (IV), - (- C alkylene - O -) - Y (IV) e) or a radical of formula (IVa), -(Calkylene - O) -C alkylene - SOCH CH2O -Y (IVa) m signifies 1 or 2, P signifies 0 or 1, Y signifies hydrogen or -SOM, q is of from 1 to 10, M signifies hydrogen or an alkali metal cation or an ammonium cation, the ammonium ...

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04-05-2017 дата публикации

Piperidinylpyrazolopyrimidinones and their use

Номер: AU2015342021A1
Принадлежит: Davies Collison Cave Pty Ltd

The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

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28-07-1994 дата публикации

Nitrogen heterocycle-substd. (meth)acrylate] ester(s)

Номер: DE0004301673A1
Принадлежит:

A process for the prodn. of (meth)acrylate esters of formula (I) comprises transesterification of esters CH2=C(R1)COOR2 (II) with cpds. (III) in the presence of a catalyst contg. Pb cpds. (IV): In the formulae R1 = H or Me; A, B = opt. branched 1-5C alkylene R2 = 1-4C alkyl.Pref. (IV) are Pb(II) cpds., esp. PbO and/or Pb(OH), and/or Pb alcoholate and/or PbCO3 and/or Pb acylate and/or corresp. basic Pb cpds., in amts. of 0.01-10 ( 0.1-1) wt.% w.r.t. reaction mixt.. (II) is methyl methacrylate (MMA) and (III) is 1-(2-hydroxyethyl)-imidazolidin-2-one (2-hydroxyethyl-ethylene urea) (IIIA). Pref., reaction is carried out for 2-10 hrs. at 50-130 deg. C. without solvent.

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18-08-1970 дата публикации

NOVEL GUANIDINE DERIVATIVES, THEIR PREPARATION AND MEDICINES CONTAINING THE SAME

Номер: BE0000746168A1
Автор:
Принадлежит:

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03-05-2012 дата публикации

NON-METAL TANNING PROCESS

Номер: WO2012055483A1
Принадлежит: CLARIANT INTERNATIONAL LTD

Tanned leather, skin or pelt is produced by non-metal tanning, comprising the step of tanning a bated hide, skin or pelt with a tanning agent (A), the tanning agent (A) being at least a mixture of compounds of formula (I) and formula (II), wherein Hal signifies fluorine or chlorine, R1 signifies hydrogen, C 1-8 -alkyl or an alkyleneoxy radical of formula (III), - (- C 2-3 alkylene - O -) q - H (III) R2 signifies a) phenyl, mono- or di-substituted with SO 3 M or COOM and optionally substituted also with hydroxyl or C 1-4 -alkyl or C 1-4 alkoxy, or b) naphthyl, mono- or di- or tri-substituted with SO 3 M and optionally substituted also with hydroxyl, or c) C 1-8 -alkylene, substituted with (S0 3 M) or (COOM), or d) a radical of formula (IV), - (- C 2-3 alkylene - O -) p - Y (IV) e) or a radical of formula (IVa), -(C 2-3 alkylene - O) p -C 2-3 alkylene - SO 2 CH 2 CH2O -Y (IVa) m signifies 1 or 2, P signifies 0 or 1, Y signifies hydrogen or -SO 3 M, q is of from 1 to 10, M signifies hydrogen or an alkali metal cation or an ammonium cation, the ammonium cation being a protonated tertiary amine or a quaternary ammonium cation, R3 signifies hydrogen or chlorine, in a tanning bath, the tanning bath having a pH of from 6 to 10 at the beginning of tanning step.

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19-06-2013 дата публикации

1,4,2-DIAZAPHOSPHOLIDINE DERIVATIVES

Номер: EP2344510B1
Автор: RICHTER, Frank
Принадлежит: Bayer Intellectual Property GmbH

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15-05-1990 дата публикации

Preparation of cyclic N,N'-dimethylureas

Номер: US0004925940A1
Принадлежит: BASF Aktiengesellschaft

Cyclic N,N'-dimethylureas are prepared by catalytic hydrogenation of a cyclic urea which carries hydroxyl groups in the α-position to the two nitrogen atoms.

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24-05-1999 дата публикации

Номер: JP0002895633B2
Автор:
Принадлежит:

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27-05-2021 дата публикации

LATENT HARDENER WITH IMPROVED STORAGE STABILITY THROUGH A DRY SURFACE TREATMENT PROCESS, ONE-COMPONENT EPOXY ADHESIVE FORMULATION COMPRISING THE SAME, AND FABRICATION METHOD THEREOF

Номер: US20210155749A1

The present specification discloses a latent hardener in which only the surface of the hardener is selectively deactivated under a carbon dioxide or inert gas atmosphere, a one-component epoxy adhesive including the same, and a preparation method thereof.

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31-10-2017 дата публикации

Oxadiazine compounds and methods of use thereof

Номер: US0009802927B2

The present disclosure relates to oxadiazine compounds, pharmaceutical compositions comprising an effective amount of an oxadiazine compound and methods for using an oxadiazine compound in the treatment of a neurodegenerative disease, comprising administering to a subject in need thereof an effective amount of an oxadiazine compound.

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07-08-2013 дата публикации

YOU COVER WITH MATS DEARILALQUILO OF 4-AMINO (REPLACED FENIL) PICOLINATOS AND 6-AMINO (REPLACED FENIL) - 4-PIRIMIDINCARBOXILATOS AND ITS USE LIKE WEED KILLERS

Номер: AR0000085019A1
Автор:
Принадлежит:

Los ésteres de arilalquilo de ácido 4-aminopicolínico y 6-amino-4-pirimidincarboxilato son herbicidas para el control de malezas en especial de aquellas especies comunes a sistemas de cultivos de arroz y trigo y en programas de manejo de pasturas.Reivindicación 1: Un compuesto de la fórmula (1) en donde Y representa alquilo C1-8, cicloalquilo C3-6 o fenilo sustituido con 1 - 4 sustituyentes seleccionados, de modo independiente, de halógeno, alquilo C1-3, cicloalquilo C3-6, alcoxi C1-3, haloalquilo C1-3, haloalcoxi C1-3, ciano, nitro, NR1R2 o donde dos sustituyentes adyacentes se toman juntos como -O(CH2)nO- u -O(CH2)n- en donde n = 1 ó 2; Z representa halógeno, alcoxi C1-3 o alquenilo C2-4; R1 y R2 representan, de modo independiente, H, alquilo C1-6, C3-6 alquenilo, C3-6 alquinilo, hidroxi, alcoxi C1-6, amino o acilo C1-6; R3 representa arilalquilo C7-11 no sustituido o sustituido.

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22-10-1979 дата публикации

NYA SUBSTITUERADE 1,3-DIARYL-2-IMINO-IMIDAZOLIDINER OCH -2-IMINO-HEXAHYDRO-PYRIMIDINER OCH SETT FOR FRAMSTELLNING DERAV

Номер: SE0007903450L
Автор:
Принадлежит:

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13-11-2014 дата публикации

HETEROCYCLYL COMPOUNDS AND USES THEREOF

Номер: WO2014181287A1
Принадлежит:

The present invention provides heterocyclyl compounds of formula I, isotopic forms, stereoisomers or tautomers thereof, or pharmaceutically acceptable salts, solvates, N- oxides, S-oxides and polymorphs thereof, and processes for their preparation. The invention further relates to pharmaceutical compositions containing the compounds and their use in the treatment of inflammatory diseases, autoimmune disorders and other related disorders. The heterocyclyl compounds find use as Interleukin 17 (IL-17) inhibitors and Tumor Necrosis Factor alpha (TNF-α) inhibitors.

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05-07-1966 дата публикации

Номер: US0003259513A1
Автор:
Принадлежит:

Подробнее
10-09-1970 дата публикации

Номер: DE0002006895A1
Автор: BREAM J, PICARD C
Принадлежит:

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11-05-1993 дата публикации

Process for the preparation of alkylimidazolidone (meth) acrylate

Номер: US0005210199A1
Принадлежит: Atochem

At least one (meth)acrylate is reacted with a heterocyclic alcohol (III) in the presence of at least one catalyst chosen from dialkyltin oxides and dialkyltin dialkoxides. Alkylimidazolidone acrylates and methacrylates are known for the part they play in the constitution of polymers which can be used as coatings and adhesives and for the treatment of paper and textiles, and for their use as agents for the treatment of leather and in the production of emulsion paints. см. иллюстрацию в PDF-документе R1 =H, CH3 ; A, B=straight or branched chain alkylene group containing from 2 to 5 carbon atoms.

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16-08-2018 дата публикации

CHIMERIC COMPOUNDS TARGETING PROTEINS, COMPOSITIONS, METHODS, AND USES THEREOF

Номер: US20180230167A1
Принадлежит:

The present invention provides chimeric compounds that modulate protein function, to restore protein homeostasis, including cytokine, aiolos, and/or ikaros activity, TNF-alpha activity, CK1-alpha activity and cell-cell adhesion. The invention provides methods of modulating protein-mediated diseases, such as cytokine-mediated diseases, disorders, conditions, or responses. Compositions, including in combination with other cytokine and inflammatory mediators, are provided. Methods of treatment, amelioration, or prevention of protein-mediated diseases, disorders, and conditions, such as cytokine-mediated diseases, disorders, and conditions, including inflammation, fibromyalgia, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, psoriasis, psoriatic arthritis, inflammatory bowel diseases, Crohn's disease, ulcerative colitis, uveitis, inflammatory lung diseases, chronic obstructive pulmonary disease, Alzheimer's disease, organ transplant rejection, and cancer, are provided. 1116.-. (canceled)118. The pharmaceutical composition of claim 117 , wherein Q is C═O.119. The pharmaceutical composition of claim 117 , wherein n is 1.120. The pharmaceutical composition of claim 117 , wherein X is C═O.121. The pharmaceutical composition of claim 117 , wherein X is CH.122. The pharmaceutical composition of claim 117 , wherein Ris H.123. The pharmaceutical composition of claim 117 , wherein R claim 117 , R claim 117 , and R claim 117 , are each independently H claim 117 , hydroxyl claim 117 , halogen claim 117 , unsubstituted Cto Calkoxy claim 117 , optionally substituted amino claim 117 , optionally substituted Cto Cheterocyclyl claim 117 , unsubstituted Cto Calkyl claim 117 , unsubstituted Cto Ccycloalkyl claim 117 , or —CF; or Ris H and R claim 117 , R claim 117 , and R claim 117 , are each independently hydroxyl claim 117 , halogen claim 117 , unsubstituted Cto Calkoxy claim 117 , optionally substituted amino claim 117 , optionally substituted Cto Cheterocyclyl claim 117 ...

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02-07-1974 дата публикации

PHENYL ACETYLIMINO-IMIDAZOLINES AND-HEXAHYDROPYRIMIDINES

Номер: US0003822262A1
Автор:
Принадлежит: SANDOZ-WANDER INC.

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09-08-1966 дата публикации

Номер: US0003265512A1
Автор:
Принадлежит:

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31-12-2019 дата публикации

Extreme ultraviolet photoresist with high-efficiency electron transfer

Номер: US0010520813B2

A method includes forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer, a sensitizer, and a photo-acid generator (PAG), wherein the sensitizer includes a resonance ring that includes nitrogen and at least one double bond. The method further includes performing an exposing process to the photoresist layer. The method further includes developing the photoresist layer, thereby forming a patterned photoresist layer.

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18-01-1983 дата публикации

1,3-Diaryl-2-imino-imidazolidines and compounds

Номер: US4369325A
Автор:
Принадлежит:

A compound of the general formula (I), (I) is described wherein R1 and R5 each represent a phenyl group optionally substituted with 1 to 3 lower alkoxy, halo, lower alkyl, monohalo-(lower)-alkyl, dihalo-(lower)-alkyl and/or trihalo-(lower)-alkyl groups, R2 stands for hydrogen or a lower alkyl group optionally substituted with a hydroxy group or 1 to 3 halogen atoms, R3 and R4 each represent a hydrogen atom or a lower alkyl group, and R6 stands for a carbamoyl, thiocarbamoyl or amidino group having optionally one or two lower alkyl and/or lower alkoxycarbonyl substitutes, or a group of the general formula R7-CO-wherein R7 stands for a lower analkoxy group, an aryloxy group, or an aralkoxy group, and n is equal to 0, provided that when R1 and R5 each represent a phenyl group, R2and R3 may not stand for hydrogen or a pharmaceutically acceptable acid addition salt, a pure isomer or an isomeric mixture thereof. The compounds posses antiphlogistic and diuretic activity.

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19-06-1991 дата публикации

Process for the preparation of alkylimidazolidone (meth)acrylate

Номер: EP0000433135A1
Принадлежит:

A compound (I) is prepared by reacting at least one (meth)acrylate (II) with a heterocyclic alcohol (III) in the presence of at least one catalyst chosen from tin dialkyloxides and/or tin dialkyldialkoxides. Alkylimidazolidone acrylates and methacrylates are known for the part they play in the constitution of polymers which are useful as coatings and adhesives and for paper and textile treatment, as well as for their use as leather treatment agents and in the production of emulsion paints. R1 = H, CH3; A,B = alkylene group with a straight or branched chain containing from 2 to 5 carbon atoms.

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08-04-2010 дата публикации

1,4,2-DIAZAPHOSPHOLIDINE DERIVATIVES

Номер: WO2010037499A1
Принадлежит: BAYER MATERIALSCIENCE AG

Die vorliegende Erfindung betrifft neuartige 1,4,2-Diazaphospholidin-Derivate, ein Verfahren zu deren Herstellung sowie die Verwendung als Katalysatoren.

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26-07-1966 дата публикации

Номер: US0003262791A1
Автор:
Принадлежит:

Подробнее
27-11-2013 дата публикации

NON-METAL TANNING PROCESS

Номер: KR1020130129175A
Автор:
Принадлежит:

Подробнее
12-09-2019 дата публикации

CHIMERIC COMPOUNDS TARGETING PROTEINS, COMPOSITIONS, METHODS, AND USES THEREOF

Номер: US20190276474A1
Принадлежит:

The present invention provides chimeric compounds that modulate protein function, to restore protein homeostasis, including cytokine, aiolos, and/or ikaros activity, TNF-alpha activity, CK1-alpha activity and cell-cell adhesion. The invention provides methods of modulating protein-mediated diseases, such as cytokine-mediated diseases, disorders, conditions, or responses. Compositions, including in combination with other cytokine and inflammatory mediators, are provided. Methods of treatment, amelioration, or prevention of protein-mediated diseases, disorders, and conditions, such as cytokine-mediated diseases, disorders, and conditions, including inflammation, fibromyalgia, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, psoriasis, psoriatic arthritis, inflammatory bowel diseases, Crohn's disease, ulcerative colitis, uveitis, inflammatory lung diseases, chronic obstructive pulmonary disease, Alzheimer's disease, organ transplant rejection, and cancer, are provided. 1116-. (canceled)118. The pharmaceutical composition of claim 117 , wherein{'sub': 1', '1', '6', '1', '6', '3', '8, 'Ris hydroxyl, halo, nitro, optionally substituted amino, optionally substituted Cto Calkoxy, optionally substituted Cto Calkyl, or optionally substituted Cto Ccarbocyclyl;'}{'sub': 2', '3', '4', '1', '6', '1', '6, 'each of R, R, and Ris independently selected from the group consisting of H, hydroxyl, halo, nitro, optionally substituted amino, optionally substituted Cto Calkoxy, and optionally substituted amino Cto Calkyl.'}119. The pharmaceutical composition of claim 118 , wherein X is C═O.120. The pharmaceutical composition of claim 118 , wherein X is CH.121. The pharmaceutical composition of claim 120 , wherein n is 1.122. The pharmaceutical composition of claim 121 , wherein Ris H.123. The pharmaceutical composition of claim 122 , wherein each of R claim 122 , R claim 122 , and Ris independently H claim 122 , hydroxyl claim 122 , halo claim 122 , nitro claim 122 , ...

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18-08-1981 дата публикации

1,3-Diaryl-2-imino-imidazolidines and compositions thereof

Номер: US0004284642A
Автор:
Принадлежит:

The invention relates to new compounds of the general formula (I), (I) wherein R1 and R5 each represent a phenyl group, optionally substituted, R2 stands for hydrogen, formyl group, carboxy group, lower alkoxycarbonyl group, hydroxy-(lower)-alkoxycarbonyl group, or a lower alkyl group, optionally substituted, R3 and R4 each represent hydrogen atom or a lower alkyl group, with the proviso that when R1 and R5 each represent a phenyl group, R2 and R3 may not stand for hydrogen. These compounds possess valuable biological properties, and can be applied primarily as antiphlogistic or diuretic agents.

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30-10-1997 дата публикации

Base-catalysed reaction of 1,3-di:isocyanato alkyl cycloalkane

Номер: DE0019644932A1
Принадлежит:

Base-catalysed reaction products of 1,3-di-isocyanato-alkylcyclohexane R1(NCO)2 in presence of acyclic urethane groups or corresponding isomeric cyclic allophanate groups (and optionally higher homologues) of formula (I) and (II) respectively, are claimed. The products are obtained by reaction of 1,3-di-isocyanato-alkylcyclohexane with polyols of formula A(OH)x. (OH)y-A-(O-CO-NH-R1)x-y-NCOn-x+y (I) A = residue of x-hydric hydroxyl compound; R1 = residue of 1,3-di-isocyanato-alkylcyclohexane; n = number of NCO equivalents in the di-isocyanate components; x = number of OH equivalents in the hydroxy components; y = (x - n) which is number of optionally unreacted OH groups, i.e. 0-4; n - x + y = number of NCO groups in the urethane of not more than 4. The NCO/OH ratio is (0.5:1)-(200:1) and the content of urethane or allophanate groups is 0.05-48 wt% based on the reaction mass used. The process comprises urethane-formation and a simultaneous or subsequent poly-addition reaction with NCO groups ...

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27-02-2020 дата публикации

Application of Imidazopyridine Derivatives in Regenerative Medicine

Номер: US20200062719A1

A method of producing a pluripotent stem cell is provided. The method is comprising contacting a non-pluripotent donor cell obtained from a mammalian donor with a compound characterized by general formulas (1) and (3). Furthermore, methods for inducing OCT4 and NANOG, increasing histone 3 lysine methylation and the maintenance of pluripotency are provided. 3. The method according to claim 1 , wherein{'sup': I', 'a', '1', '2', '3', '4', 'o', 'm', 'p', 'm′', 'o′, 'sub': 3', '2, 'each R, R, R, R, R, R, R, R, R, R and R is independently selected from —H, —CH, —F, —Cl, —Br, —I, —OH, —NO, —CN or —OMe.'}4. The method according to claim 1 , wherein{'sup': '1', 'sub': '3', 'Ris selected from —CH, and —H;'}{'sup': '2', 'sub': '3', 'Ris selected from —CH, and —H;'}{'sup': '3', 'sub': '3', 'Ris selected from —CH, —H, —F, —Cl, and —Br;'}{'sup': '4', 'sub': '3', 'Ris selected from —CH, and —H;'}{'sup': o', 'o′, 'sub': '2', 'Rand R are selected from —NO, —F, and —H;'}{'sup': 'p', 'sub': 3', '2, 'Ris selected from —CH, —F, —Cl, —Br, —NO, —OMe, —OH, —CN, and —H;'}{'sup': m', 'm′, 'sub': '2', 'Rand R are selected from —Cl, —H, —F, —OH, —NO, and —OMe, and/or'}{'sup': 'z', 'Ris selected from —H and formula (2).'}5. The method according to claim 1 , wherein the compound according to formula (1) isa) N,N-dimethyl-2-(6-methyl-2-p-tolylimidazo[1,2-a]pyridine-3-yl)acetamid (100),b) 6-methyl-2-(p-tolyl)imidazo[1,2-a]pyridine (101),c) 2-(4-fluorophenyl)-6-methyl-imidazo[1,2-a]pyridine (102),d) 2-(4-chlorophenyl)-6-methyl-imidazo[1,2-a]pyridine (103),e) 2-(4-bromophenyl)-6-methyl-imidazo[1,2-a]pyridine (104),f) 6-methyl-2-(4-nitrophenyl)imidazo[1,2-a]pyridine (105),g) 2-(4-methoxyphenyl)-6-methyl-imidazo[1,2-a]pyridine (106),h) 4-(6-methylimidazo[1,2-a]pyridin-2-yl)phenol (107),i) 4-(6-methylimidazo[1,2-a]pyridin-2-yl)benzonitrile (108),j) 6-methyl-2-phenyl-imidazo[1,2-a]pyridine (109),k) 6-methyl-2-(3-nitrophenyl)imidazo[1,2-a]pyridine (110),l) 6-methyl-2-(2-nitrophenyl)imidazo[1,2-a]pyridine ...

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25-01-2018 дата публикации

COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE AND ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

Номер: US20180026205A1
Принадлежит:

Disclosed are a composition for an organic optoelectronic device includes at least one of a first host compound represented by a combination of Chemical Formula 1 and Chemical Formula 2, and at least one of a second host compound represented by a combination of Chemical Formula 3 and Chemical Formula 4, and an organic optoelectronic device including the same, and a display device. 5. The composition for an organic optoelectronic device as claimed in claim 4 , wherein the Arto Arare independently a substituted or unsubstituted phenyl group claim 4 , a substituted or unsubstituted biphenyl group claim 4 , a substituted or unsubstituted terphenyl group claim 4 , a substituted or unsubstituted naphthyl group claim 4 , or a substituted or unsubstituted triphenylene group claim 4 ,{'sup': '1', 'the Lis a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group,'}{'sup': 1', '3', '6', '11, 'Rto Rand Rto Rare independently hydrogen, deuterium, a substituted or unsubstituted C1 to C4 alkyl group, a substituted or unsubstituted phenyl group, or a combination thereof, and'}the “substituted” refers to replacement of at least one hydrogen by deuterium, a C1 to C4 alkyl group, or a C6 to C12 aryl group.7. The composition for an organic optoelectronic device as claimed in claim 6 , wherein the Land Lare independently a single bond claim 6 , a substituted or unsubstituted phenylene group claim 6 , a substituted or unsubstituted biphenylene group claim 6 , a substituted or unsubstituted terphenylene group claim 6 , or a substituted or unsubstituted quaterphenylene group claim 6 ,the ET is a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted triazinyl group, or a substituted or unsubstituted quinazolyl group,{'sup': 1', '2, 'the Yand Yare independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a ...

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23-04-2020 дата публикации

Extreme Ultraviolet Photoresist With High-Efficiency Electron Transfer

Номер: US20200124964A1
Принадлежит:

A method includes forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer, a sensitizer, and a photo-acid generator (PAG), wherein the sensitizer includes a resonance ring that includes nitrogen and at least one double bond. The method further includes performing an exposing process to the photoresist layer. The method further includes developing the photoresist layer, thereby forming a patterned photoresist layer. 1. A method comprising:forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer, a sensitizer, and a photo-acid generator (PAG), wherein the sensitizer includes a resonance ring that includes nitrogen and at least one double bond;performing an exposing process to the photoresist layer;performing a thermal treatment to the photoresist layer; anddeveloping the photoresist layer, thereby forming a patterned photoresist layer.2. The method of claim 1 , wherein the sensitizer is chemically bonded to the PAG.3. The method of claim 1 , wherein the resonance ring includes at least two nitrogen atoms.4. The method of claim 1 , wherein the sensitizer includes a second resonance ring containing nitrogen and at least one double bond.5. The method of claim 1 , wherein the sensitizer has an electron recombination energy within a range of about 165-170 kilocalories/mol.6. The method of claim 1 , wherein the sensitizer is an aromatic structure.7. The method of claim 1 , wherein the sensitizer includes a heterocyclic structure.8. The method of claim 1 , wherein the sensitizer includes a polar group of at least one of —OH claim 1 , —NH2 claim 1 , COOH claim 1 , and CONH2.9. The method of claim 1 , wherein the PAG comprises an absorb group that includes a structure with a plurality of rings claim 1 , wherein at least one of the rings is heterocyclic and includes at least one double bond.10. The method of claim 9 , wherein the structure includes one of: sulfur claim 9 , iodine claim 9 , or carbon.11 ...

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07-08-2014 дата публикации

1 4,2-diazaphospholidine derivatives

Номер: US20140221650A1
Автор: Frank Richter
Принадлежит: BAYER MATERIALSCIENCE AG

The present invention relates to novel 1,4,2-diazaphospholidine derivatives, to a process for preparation thereof and to use as catalysts.

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21-06-2018 дата публикации

Extreme Ultraviolet Photoresist With High-Efficiency Electron Transfer

Номер: US20180173101A1

A method includes forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer, a sensitizer, and a photo-acid generator (PAG), wherein the sensitizer includes a resonance ring that includes nitrogen and at least one double bond. The method further includes performing an exposing process to the photoresist layer. The method further includes developing the photoresist layer, thereby forming a patterned photoresist layer.

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09-11-2017 дата публикации

PROCESS FOR THE PREPARATION OF BREXPIPRAZOLE AND INTERMEDIATES THEREOF

Номер: US20170320862A1
Принадлежит: CADILA HEALTHCARE LIMITED

The present invention relates to Brexpiprazole having a purity of about 99.5% or more by area percentage of HPLC, having total impurities not more than 0.5% relative to brexpiprazole as measured by area percentage of HPLC, and having less than 0.1% 1-(benzo[b]thiophen-4-yl)piperazine or a salt thereof relative to brexpiprazole by area percentage of HPLC. The present invention also provides a composition comprising brexpiprazole having 1-(benzo[b]thiophen-4-yl)-piperazine or a salt thereof in an amount less than about 0.1% relative to brexpiprazole by area percentage of HPLC and process for the preparation of brexpiprazole. 1. Brexpiprazole having a purity of about 99.5% or more by area percentage of HPLC.2. The brexpiprazole according to having total impurities of not more than 0.5% relative to brexpiprazole as measured by area percentage of HPLC.3. The brexpiprazole according to having less than 0.1% 1-(benzo[b]thiophen-4-yl) piperazine or a salt thereof relative to brexpiprazole by area percentage of HPLC.4. The brexpiprazole according to substantially free from one: or more of7-(4-(4-(benzo[b]thiophen-4-yl)piperazin-1-yl)butoxy)-1-(4-(4-(benzo-[b]thiophen-4-yl) piperazin-1-yl)butyl)quinolin-2(1H)-one (impurity-S); 2,7-bis(4-(4-(benzo[b]thiophen-4-yl) piperazin-1-yl)butoxy)quinoline (impurity-T); and 7-(4-(4-(benzo[b]thiophen-4-yl) piperazin-1-yl)butoxy)-1,2-dihydro-quinoline(impurity-U), relative to brexpiprazole by area percentage of HPLC.5. The brexpiprazole according to claim 1 , which is crystallized from toluene.6. The brexpiprazole according to claim 5 , which is substantially free from residual solvents.7. The brexpiprazole according to claim 1 , comprising crystallizing brexpiprazole in one or more solvents.8. The brexpiprazole according to wherein the solvent comprises one or more of water claim 7 , methanol claim 7 , ethanol claim 7 , isopropanol claim 7 , butanol claim 7 , acetone claim 7 , methyl ethyl ketone claim 7 , methyl isobutylketone claim 7 , ...

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23-11-2017 дата публикации

Piperidinylpyrazolopyrimidinones and their use

Номер: US20170334917A1
Принадлежит: Bayer Pharma AG

The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

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23-11-2017 дата публикации

CHIMERIC COMPOUNDS TARGETING PROTEINS, COMPOSITIONS, METHODS, AND USES THEREOF

Номер: US20170334932A1
Принадлежит:

The present invention provides chimeric compounds that modulate protein function, to restore protein homeostasis, including cytokine, aiolos, and/or ikaros activity, TNF-alpha activity, CK1-alpha activity and cell-cell adhesion. The invention provides methods of modulating protein-mediated diseases, such as cytokine-mediated diseases, disorders, conditions, or responses. Compositions, including in combination with other cytokine and inflammatory mediators, are provided. Methods of treatment, amelioration, or prevention of protein-mediated diseases, disorders, and conditions, such as cytokine-mediated diseases, disorders, and conditions, including inflammation, fibromyalgia, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, psoriasis, psoriatic arthritis, inflammatory bowel diseases, Crohn's disease, ulcerative colitis, uveitis, inflammatory lung diseases, chronic obstructive pulmonary disease, Alzheimer's disease, organ transplant rejection, and cancer, are provided. 2116-. (canceled)117. The compound of claim 1 , wherein Q is C═O.118. The compound of claim 117 , wherein n is 1.119. The compound of claim 117 , wherein X is C═O.120. The compound of claim 117 , wherein X is CH.121. The compound of claim 117 , wherein Ris H.122. The compound of claim 117 , wherein R claim 117 , R claim 117 , R claim 117 , and R claim 117 , are each independently H claim 117 , hydroxyl claim 117 , halogen claim 117 , unsubstituted Cto Calkoxy claim 117 , optionally substituted amino claim 117 , optionally substituted Cto Cheterocyclyl claim 117 , unsubstituted Cto Calkyl claim 117 , unsubstituted Cto Ccycloalkyl claim 117 , or —CF.123. The compound of claim 122 , wherein R claim 122 , R claim 122 , R claim 122 , and R claim 122 , are each independently H claim 122 , hydroxyl claim 122 , halogen claim 122 , unsubstituted Cto Calkoxy claim 122 , unsubstituted Cto Calkyl claim 122 , optionally substituted Cto Cheterocyclyl claim 122 , or —CF.124. The compound of claim 117 , ...

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28-12-1971 дата публикации

Lubricating oils and fuels containing acylated nitrogen additives

Номер: US3630904A
Принадлежит: Lubrizol Corp

COMPOSITIONS OF MATTER PARTICULARLY USEFUL AS LUBRICANT AND FUEL ADDITIVES PREPARED BY REACTING VARIOUS NITROGENCONTAINING REACTANTS WITH A MONO-OR POLYCARBOXYLIC ACID ACYLATING AGENT CONTAINING AT LEAST ABOUT THIRTY ALIPHATIC CARBON ATOMS. THE NITROGEN-CONTAINING REACTANTS ARE CHARACTERIZED BY THE PRESENCE OF AT LEAST ONE N-SUBSTITUENT CORRESPONDING TO WHERE R IS 1-10 AND R'''' IS HYDROCARBYLENE OF UP TO 10 CARBON ATOMS. AN EXEMPLARY COMPOSITION IS ONE PREPARED BY REACTING POLYISOBUTENYL SUCCINIC ANHYDRIDE WITH THE REACTION PRODUCT OF N-(HYDROXYETHYL)-ETHYLENE DIAMINE AND ADIPIC ACID.

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04-12-2013 дата публикации

Arylalkyl esters of 4-amino-6-(substituted phenyl)picolinates and 6-amino-2-(substituted phenyl)-4-pyrimidinecarboxylates and their use as herbicides

Номер: EP2667716A1
Принадлежит: DOW AGROSCIENCES LLC

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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27-10-2015 дата публикации

Arylalkyl esters of 4-amino-6-(substituted phenyl)-picolinates and 6-amino-2-(substituted phenyl)-pyrimidinecarboxylates and their use as selective herbicides for crops

Номер: US9169217B2
Принадлежит: DOW AGROSCIENCES LLC

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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29-07-2015 дата публикации

Arylalkyl esters of 4-aminopicolinates and their use as herbicides

Номер: EP2899182A1
Принадлежит: DOW AGROSCIENCES LLC

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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11-12-2013 дата публикации

Arylalkyl esters of 4-mino-6-(substituted phenyl)picolinates, arylalkyl esters of 6-amino-2-(substituted phenyl)-4-pyrimidinecarboxylates, and applications thereof as herbicides

Номер: CN103442570A
Принадлежит: DOW AGROSCIENCES LLC

4-氨基吡啶-2-甲酸的芳烷基酯和6-氨基-嘧啶-4-甲酸的芳烷基酯是用于防治杂草的除草剂,尤其是对于稻和小麦种植制度常见的并且在牧草管理规划中的杂草物种。

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06-08-2015 дата публикации

Arylalkyl esters of 4-amino-6-(substituted phenyl)picolinates and 6-amino-2-(substituted phenyl)-4-pyrimidinecarboxylates and their use as herbicides

Номер: KR101542313B1

4-아미노피콜린산 및 6-아미노-4-피리미딘카르복실레이트의 아릴알킬 에스테르는 특히 쌀 및 밀과 같은 종의 경작 시스템 및 목초지 관리 프로그램에서의, 잡초 제어를 위한 제초제이다. The arylalkyl esters of 4-aminopicolinic acid and 6-amino-4-pyrimidinecarboxylate are herbicides for weed control, especially in the cultivation systems and grassland management programs of species such as rice and wheat.

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02-08-2012 дата публикации

Arylalkyl esters of 4-amino-6-(substituted phenyl)picolinates and 6-amino-2-(substituted phenyl)-4-pyrimidinecarboxylates and their use as herbicides

Номер: WO2012103042A1
Принадлежит: DOW AGROSCIENCES LLC

Arylalkyl esters of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are herbicides for control of weeds especially those species common to rice and wheat cropping systems and in pasture management programs.

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27-11-2019 дата публикации

Composition for organic optoelectronic device and organic optoelectronic device and display device

Номер: KR102049419B1
Принадлежит: 삼성에스디아이 주식회사

화학식 1 및 화학식 2의 조합으로 표현되는 적어도 1종의 제1 호스트 화합물, 그리고 화학식 3 및 하기 화학식 4의 조합으로 표현되는 적어도 1종의 제2 호스트 화합물을 포함하는 유기 광전자 소자용 조성물, 이를 적용한 유기 광전자 소자 및 표시 장치에 관한 것이다. 상기 화학식 1 내지 4에 대한 상세 내용은 명세서에서 정의한 바와 같다. Composition for an organic optoelectronic device comprising at least one first host compound represented by a combination of Formula 1 and Formula 2, and at least one second host compound represented by a combination of Formula 3 and Formula 4, An organic optoelectronic device and a display device. Details of the Chemical Formulas 1 to 4 are as defined in the specification.

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16-04-1995 дата публикации

PROCEDURE FOR THE PREPARATION OF (MET) ALKYLIMIDAZOLIDONE ACRYLATE.

Номер: ES2068364T3
Принадлежит: Elf Atochem SA

SE PREPARA UN COMPUESTO (I) HACIENDO REACCIONAR AL MENOS UN (MET)ACRILATO (II) CON UN ALCOHOL HETEROCICLICO (III), EN PRESENCIA DE AL MENOS UN CATALIZADOR ELEGIDO ENTRE LOS DIALKILOXIDOS DE ESTAÑO, LOS DIALKILDIALCOXIDOS DE ESTAÑO. LOS ACRILATOS Y METACRILATOS DE ALKILIMIDAZOLIDONA SON CONOCIDOS POR SU PAPEL EN LA CONSTITUCION DE POLIMEROS UTILES COMO REVESTIMIENTOS Y ADHESIVOS, Y PARA EL TRATAMIENTO DEL PAPEL Y DE LOS TEXTILES, ASI COMO PARA SU UTILIZACION COMO AGENTES DE TRATAMIENTO DEL CUERO Y EN LA PRODUCCION DE PINTURAS EN EMULSION. R SUB 1 = H, C SUB 3, A, B= GRUPO ALKILENO DE CADENA RECTA O RAMIFICADA QUE TIENE ENTRE 2 Y 5 ATOMOS DE CARBONO. A COMPOUND (I) IS PREPARED BY REACTING AT LEAST ONE (MET) ACRYLATE (II) WITH A HETERO CYCLIC ALCOHOL (III), IN THE PRESENCE OF AT LEAST ONE CATALYST CHOSEN AMONG THE TIN DIALKYLOXIDES. THE ACRYLATES AND METHACRYLATES OF ALKYLIMIDAZOLIDONE ARE KNOWN FOR THEIR ROLE IN THE CONSTITUTION OF USEFUL POLYMERS AS COATINGS AND ADHESIVES, AND FOR THE TREATMENT OF PAPER AND TEXTILE PRODUCTS, AS WELL AS A TREATMENT AND PURIFICATION AGENT. IN EMULSION. R SUB 1 = H, C SUB 3, A, B = ALKYLENE GROUP OF STRAIGHT OR BRANCHED CHAIN THAT HAS BETWEEN 2 AND 5 CARBON ATOMS.

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15-08-1979 дата публикации

PROCEDURE FOR PREPARING ADDITIVES FOR LUBRICANTS AND FUELS.

Номер: NL161180B
Автор:
Принадлежит: Lubrizol Corp

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31-03-2022 дата публикации

Pyrimidyl derivative, preparation method therefor and use thereof

Номер: WO2022063212A1
Принадлежит: 广州费米子科技有限责任公司

A pyrimidyl derivative, a preparation method therefor and the use thereof. The pyrimidyl derivative has a structure as represented by general formula (I). The pyrimidyl derivative can be used as a selective CDK7 inhibitor to address the effective treatment requirements of multiple cancers, especially transcription-dysregulated cancers. <img file="dest_path_image002.jpg" he="53.18" img-content="drawing" img-format="jpg" inline="yes" orientation="portrait" wi="106.89"/>

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13-09-2017 дата публикации

Piperidinylpyrazolopyrimidinones and their use

Номер: EP3215505A1
Принадлежит: Bayer Pharma AG

The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

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29-09-1971 дата публикации

Improvements in or relating to organic compounds

Номер: ZA701134B
Автор: C Picard, J Bream
Принадлежит: Wander A

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01-07-2018 дата публикации

Method for lithography patterning

Номер: TW201823865A
Автор: 林進祥, 王建惟, 賴韋翰

方法包括形成光阻層於基板上,其中光阻層包含聚合物、光敏劑、與光酸產生劑,其中光敏劑包含共振環,且共振環包含氮與至少一雙鍵。方法亦包括對光阻層進行曝光製程。方法亦包括顯影光阻層以形成圖案化的光阻層。

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06-11-2014 дата публикации

Tanning process without metal

Номер: ES2519366T3
Принадлежит: Stahl International BV

Un proceso para la producción de cuero, pieles o pelambres curtidos mediante curtido sin metal, que comprende el paso de curtir un pellejo, piel o pelambre macerados con un agente curtiente (A), y el agente curtiente (A) es al menos una mezcla de los compuestos de fórmula (I) y fórmula (II),**Fórmula** en las cuales Hal significa flúor o cloro, R1 significa hidrógeno, alquilo de C1-8 o un radical alquilenoxi de fórmula (III), -(-alquileno de C2-3 -O-)q-H (III) R2 significa a) fenilo, mono- o di-sustituido con SO3M o COOM y opcionalmente sustituido también con hidroxilo o alquilo de C1- 4 o alcoxi de C1-4, o b) naftilo, mono- o di- o tri-sustituido con SO3M y opcionalmente sustituido también con hidroxilo, o c) alquileno de C1-8, sustituido con (SO3M) o (COOM), o d) un radical de fórmula (IV), - (-alquileno de C2-3 - O -)p - Y (IV) e) o un radical de fórmula (IVa), -(alquileno de C2-3-O)p-alquileno de C2-3-SO2CH2CH2O-Y (IVa) m significa 1 o 2, p significa 0 o 1, Y significa hidrógeno o -SO3M, q es de 1 a 10, M significa hidrógeno o un catión de metal alcalino o un catión amonio, y el catión amonio es una amina terciaria protonizada o un catión de amonio cuaternario, R3 significa hidrógeno o cloro, en un baño de curtido, el baño de curtido tiene un pH de 6 a 10 al inicio del paso de curtiembre.

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01-06-2016 дата публикации

PIPERIDINILPIRAZOLOPIRIMIDINONAS AND USE OF THE SAME

Номер: UY36385A
Принадлежит: Bayer Pharma AG

La presente solicitud de patente se refiere a novedosas piperidinilpirazolopirimidinonas sustituidas, a los procesos para la preparación de las mismas, a los compuestos que pueden utilizarse en forma aislada o combinada en un método para el tratamiento y/o la profilaxis de enfermedades, en particular para el tratamiento y/o la profilaxis de sangrado agudo y recurrente en pacientes con o sin trastornos hemostáticos hereditarios o adquiridos subyacentes, donde el sangrado está asociado con una enfermedad o intervención médica a seleccionar a partir del conjunto que consiste en sangrado menstrual abundante, hemorragia post parto, shock hemorrágico, cistitis hemorrágicas, hemorragia gastrointestinal, etc.

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29-06-2018 дата публикации

The method of lithographic patterning

Номер: CN108227409A
Автор: 林进祥, 王建惟, 赖韦翰

光刻图案化的方法包括形成光致抗蚀剂层于基板上,其中光致抗蚀剂层包含聚合物、光敏剂、与光酸产生剂,其中光敏剂包含共振环,且共振环包含氮与至少一双键。方法亦包括对光致抗蚀剂层进行曝光工艺。方法亦包括显影光致抗蚀剂层以形成图案化的光致抗蚀剂层。

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27-06-2019 дата публикации

Five-membered heteroaryl ring derivative, pharmaceutical composition containing same, and application thereof

Номер: WO2019120256A1
Принадлежит: 上海迪诺医药科技有限公司

本发明公开了一种五元杂芳环衍生物(I)、其异构体、溶剂合物、溶剂合物的晶型、前药、稳定的同位素衍生物或药学上可接受的盐。本发明的五元杂芳环衍生物具有良好的IDO抑制作用,可以有效治疗、缓解和/或预防由于免疫抑制所引起的各种相关疾病,例如肿瘤、传染性疾病及自身免疫类疾病等。

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06-12-1979 дата публикации

Imidazolidine and hexahydropyrimidine derivatives

Номер: JPS54154765A
Принадлежит: Egyt Gyogyszervegyeszeti Gyar

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12-07-2017 дата публикации

PIPERIDINYLpyrazolOPYRIMIDINONES AND THE USE OF THEM

Номер: PE20170920A1
Принадлежит: Bayer Pharma AG

Se refiere a un compuesto de formula (I-A) o (I-B), donde: R1 es hidrogeno o alquilo C1-C5; R2 es hidrogeno, alquilo C1-C4, entre otros; R3 es hidrogeno, halogeno, entre otros. Tambien se refiere a un procedimiento para su preparacion. Dichos compuestos son piperidinilpirazolopirimidinonas sustituidas utiles en el tratamiento de sangrado agudo y recurrente en pacientes con o sin trastornos hemostaticos hereditarios o adquiridos Refers to a compound of formula (I-A) or (I-B), where: R1 is hydrogen or C1-C5 alkyl; R2 is hydrogen, C1-C4 alkyl, among others; R3 is hydrogen, halogen, among others. It also refers to a procedure for its preparation. Said compounds are substituted piperidinylpyrazolopyrimidinones useful in the treatment of acute and recurrent bleeding in patients with or without inherited or acquired hemostatic disorders.

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29-10-2014 дата публикации

Non-metal tanning process

Номер: CN102933725B
Принадлежит: CLARIANT INTERNATIONAL LTD

在鞣制浴中通过非金属鞣制制备鞣制皮革、小皮或生皮,包括用鞣剂(A)鞣制软化的大皮、小皮或生皮的步骤,所述鞣剂(A)为至少式(I)和(II)化合物的混合物;其中,Hal表示氟或氯;R1表示H、C 1-8 烷基或式(III)的亚烷氧基:-(-C 2-3 亚烷基-O-) q -H(III);R2表示a)苯基,其被SO 3 M或COOM单-或二取代且任选也被羟基或C 1-4 烷基或C 1-4 烷氧基取代;或b)萘基,其被SO 3 M单-、二-或三取代且任选也被羟基取代;或c)C 1-8 亚烷基,其被SO 3 M或COOM取代;或d)式(IV)的基团-(-C 2-3 亚烷基-O-) p -Y(IV),e)或式(IVa)的基团-(C 2-3 亚烷基-O) p -C 2-3 亚烷基-SO 2 CH 2 CH 2 O–Y(IVa);m表示1或2;p表示0或1;Y表示氢或-SO 3 M;q为1-10;M表示氢、碱金属阳离子或铵阳离子,所述铵阳离子为质子化的叔胺或季铵阳离子;R3表示氢或氯;所述鞣制浴在鞣制步骤开始时的pH值为6-10。 ;-(-C 2-3 亚烷基-O-) q -H (III);-(-C 2-3 亚烷基-O-) p -Y (IV);-(C 2-3 亚烷基-O) p -C 2-3 亚烷基-SO 2 CH 2 CH 2 O–Y (IVa)。

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05-07-1966 дата публикации

Anti-stripping agents

Номер: US3259513A
Принадлежит: Petrolite Corp

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16-06-2022 дата публикации

Chemical process

Номер: TW202222163A
Принадлежит: 瑞士商先正達農作物保護公司

本發明尤其提供了一種用於生產具有式 (I) 之化合物之方法

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22-03-2024 дата публикации

哒嗪酮类化合物

Номер: CN117751108A
Принадлежит: Medshine Discovery Inc

一系列哒嗪酮类化合物及其药学上可接受的盐,及其在制备治疗相关疾病的药物中的应用,具体公开了式(IV)化合物及其药学上可接受的盐。

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21-02-2024 дата публикации

三并環類化合物製備方法及其中間體

Номер: TWI833610B

本發明公開了三并環類化合物製備方法及其中間體,具體地,公開了一種製備式(I-10)所示化合物或其光學異構體的方法,其中,將式(I-8)所示化合物與式(I-9)所示化合物進行接觸,獲得式(I-10)所示化合物或其光學異構體,該製備方法簡單,收率高。 , ,

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01-10-2023 дата публикации

三并環類化合物製備方法及其中間體

Номер: TW202337887A

本發明公開了三并環類化合物製備方法及其中間體,具體地,公開了一種製備式(I-10)所示化合物或其光學異構體的方法,其中,將式(I-8)所示化合物與式(I-9)所示化合物進行接觸,獲得式(I-10)所示化合物或其光學異構體,該製備方法簡單,收率高。 , ,

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07-11-2023 дата публикации

Extreme ultraviolet photoresist with high-efficiency electron transfer

Номер: US11809080B2

A method includes forming a photoresist layer over a substrate, wherein the photoresist layer includes a polymer, a sensitizer, and a photo-acid generator (PAG), wherein the sensitizer includes a resonance ring that includes nitrogen and at least one double bond. The method further includes performing an exposing process to the photoresist layer. The method further includes developing the photoresist layer, thereby forming a patterned photoresist layer.

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20-07-2011 дата публикации

1,4,2-diazaphospholidin-derivate

Номер: EP2344510A1
Автор: Frank Richter
Принадлежит: BAYER MATERIALSCIENCE AG

Die vorliegende Erfindung betrifft neuartige 1,4,2-Diazaphospholidin-Derivate, ein Verfahren zu deren Herstellung sowie die Verwendung als Katalysatoren.

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25-08-2011 дата публикации

1,4,2-diazaphospholidine derivatives

Номер: US20110207927A1
Автор: Frank Richter
Принадлежит: BAYER MATERIALSCIENCE AG

The present invention relates to novel 1,4,2-diazaphospholidine derivatives, to a process for preparation thereof and to use as catalysts.

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31-08-2011 дата публикации

1,4,2-二氮杂磷杂环戊烷衍生物

Номер: CN102171231A
Автор: F·里希特
Принадлежит: BAYER MATERIALSCIENCE AG

本发明涉及新型1,4,2-二氮杂磷杂环戊烷衍生物,涉及制备它的方法和涉及作为催化剂的用途。

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04-06-2014 дата публикации

1,4,2-二氮杂磷杂环戊烷衍生物

Номер: CN102171231B
Автор: F·里希特
Принадлежит: BAYER MATERIALSCIENCE AG

本发明涉及新型1,4,2-二氮杂磷杂环戊烷衍生物,涉及制备它的方法和涉及作为催化剂的用途。

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05-01-2024 дата публикации

一种杂环衍生物及其在医药上的应用

Номер: CN117355508A
Принадлежит: Tibet Haisike Pharmaceutical Co ltd

涉及一种通式(I)所述的化合物或者其立体异构体、互变异构体、氘代物、溶剂化物、前药、代谢产物、药学上可接受的盐或共晶,及其中间体和制备方法,以及在制备治疗与JAK激酶活性或表达量相关疾病的药物中的应用。

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31-03-2022 дата публикации

Proceso químico para la síntesis de compuestos de piridazina sustituidos

Номер: UY39381A
Принадлежит: SYNGENTA CROP PROTECTION AG

La presente invención proporciona, entre otras cosas, un proceso para producir un compuesto de fórmula (I) donde los sustituyentes son tal como se definen en la reivindicación 1. La presente invención proporciona además compuestos intermedios utilizados en dicho proceso y métodos para producir dichos compuestos intermedios.

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17-02-2022 дата публикации

Process for the preparation of pyridazinone derivatives

Номер: CA3188929A1
Принадлежит: Syngenta Crop Protection AG Switzerland

The present invention provides, inter alia, a process for producing a compound of formula (I) wherein the substituents are as defined in claim 1. The present invention further provides intermediate compounds utilised in said process, and methods for producing said intermediate compounds.

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14-03-2023 дата публикации

Processo para a preparação de derivados de piridazinona

Номер: BR112023002696A2
Принадлежит: SYNGENTA CROP PROTECTION AG

PROCESSO PARA A PREPARAÇÃO DE DERIVADOS DE PIRIDAZINONA. A presente invenção proporciona, entre outros, um processo para produzir um composto da fórmula (I) em que os substituintes são como definidos na reivindicação 1. A presente invenção proporciona adicionalmente compostos intermediários utilizados no referido processo e métodos para produzir os referidos compostos intermediários.

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02-03-2023 дата публикации

Process for the preparation of pyridazinone derivatives

Номер: AU2021324123A1
Принадлежит: Syngenta Crop Protection AG Switzerland

The present invention provides, inter alia, a process for producing a compound of formula (I) wherein the substituents are as defined in claim 1. The present invention further provides intermediate compounds utilised in said process, and methods for producing said intermediate compounds.

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12-05-2023 дата публикации

哒嗪酮衍生物的制备方法

Номер: CN116113630A
Принадлежит: Syngenta Crop Protection AG Switzerland

本发明尤其提供了一种用于生产具有式(I)的化合物的方法,其中取代基如权利要求1中所定义。本发明进一步提供了在所述方法中使用的中间体化合物、以及用于生产所述中间体化合物的方法。

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14-09-2023 дата публикации

ピリダジノン誘導体の調製プロセス

Номер: JP2023539451A

本発明はとりわけ、式(I)の化合物(ここで、置換基は請求項1に定義されているとおりである)を生成するプロセスを提供する。本発明はさらに、前記プロセスにおいて用いられる中間体化合物、及び、前記中間体化合物を生成する方法を提供する。【化1】TIFF2023539451000137.tif41150

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21-06-2023 дата публикации

Process for the preparation of pyridazinone derivatives

Номер: EP4196474A1
Принадлежит: Syngenta Crop Protection AG Switzerland

The present invention provides, inter alia, a process for producing a compound of formula (I) wherein the substituents are as defined in claim 1. The present invention further provides intermediate compounds utilised in said process, and methods for producing said intermediate compounds.

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15-03-1995 дата публикации

Verfahren zur herstellung von alkylimidazolidone(meth)acrylat.

Номер: ATE118486T1
Принадлежит: Atochem Elf Sa

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17-04-2023 дата публикации

피리다지논 유도체의 제조 공정

Номер: KR20230051228A
Принадлежит: 신젠타 크롭 프로텍션 아게

본 발명은 특히 화학식 I의 화합물의 제조 공정을 제공한다: [화학식 I] (상기 식에서, 치환기는 제1항에 정의된 바와 같음). 본 발명은 상기 공정에 이용되는 중간체 화합물 및 상기 중간체 화합물의 제조 방법을 추가로 제공한다.

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11-03-2020 дата публикации

Improvements in or relating to curing agents

Номер: GB2576875A
Принадлежит: Hexcel Composites Ltd

A curative composition comprising a combination of adipic acid dihydrazide and/or isophthalic dihydrazide and a clathrate in which the guest compound of the clathrate comprises an imidazole, an imidazoline or diazabicycloalkanes (DBCA). Also disclosed is a resin formulation comprising a thermosetting resin, e.g. epoxy resin, and the curative composition and use of the resin formulation as a matrix in fibre reinforced composites.

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22-07-2022 дата публикации

苯并咪唑化合物及其用途

Номер: CN114773331A

本发明提出了一种有效抑制IRAK4活性的新化合物,其为式I所示化合物、其互变异构体、立体异构体、水合物、溶剂化物、药学上可接受的盐或前药,其制备方法,以及其在制备药物中的用途。

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11-01-2024 дата публикации

Process for the preparation of pyridazinone derivatives

Номер: US20240010637A1
Принадлежит: Syngenta Crop Protection AG Switzerland

The present invention provides, inter alia, a process for producing a compound of formula (I) wherein the substituents are as defined in claim 1 . The present invention further provides intermediate compounds utilised in said process, and methods for producing said intermediate compounds.

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17-10-2018 дата публикации

Improvements in or relating to curing agents

Номер: GB201814139D0
Автор:
Принадлежит: Hexcel Composites Ltd

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01-07-2021 дата публикации

Improvements in or relating to curing agents

Номер: US20210198420A1
Принадлежит: Hexcel Composites Ltd

A curative system comprising a combination of adipic acid dihydrazide and/or isophthalic dihydrazide and a clathrate in which the guest compound of the clathrate comprises an imidazole, an imidazoline or diazabicycloalkanes (DBCA).

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22-04-2021 дата публикации

Methods and compositions for treating urea cycle disorders

Номер: US20210114996A1
Принадлежит: Camp4 Therapeutics Corp

Provided are methods and compositions for the treating a patient with a urea cycle disorder. Methods and compositions are also provided for modulating genes encoding enzymes that participate in the urea cycle by altering gene signaling networks.

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04-04-2023 дата публикации

유기 재료 조성물 및 그 응용

Номер: KR20230044349A

본 발명은 유기 재료 조성물 및 그 응용에 대해 제공하고, 함유된 화합물 사이의 배합을 통해 이루어진 상기 유기 재료 조성물을 유기 기능층 재료로 할 경우, 소자는 낮은 구동 전압, 높은 전류 효율 및 높은 수명을 가질 수 있게 된다.

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