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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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Форма поиска

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 45. Отображено 45.
01-06-2004 дата публикации

Process for imidazo[4,5-c]pyridin-4-amines

Номер: US0006743920B2

A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 4-phenoxy-1H-imidazo[4,5-c]pyridine and aminating the 4-phenoxy-1H-imidazo[4,5-c]pyridine to provide a 1H-imidazo[4,5-c]pyridin-4-amine.

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18-06-2009 дата публикации

ELECTRET WEBS WITH CHARGE-ENHANCING ADDITIVES

Номер: CA0002708117A1
Принадлежит:

Electret webs are presented which include a blend of a thermoplastic resin and a charge additive. The charge additives include ester-substituted and amide-substituted trianilino triazine materials. The webs prepared from the blends may be in the form of films or non-woven fibrous webs. Non-woven microfiber webs are useful as filtration media.

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17-11-2011 дата публикации

Electret webs with charge-enhancing additives

Номер: AU2008335536B2
Принадлежит:

Electret webs are presented which include a blend of a thermoplastic resin and a charge additive. The charge additives include ester-substituted and amide-substituted trianilino triazine materials. The webs prepared from the blends may be in the form of films or non-woven fibrous webs. Non-woven microfiber webs are useful as filtration media.

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25-08-2015 дата публикации

ELECTRET WEBS WITH CHARGE-ENHANCING ADDITIVES

Номер: CA0002708117C

Electret webs are presented which include a blend of a thermoplastic resin and a charge additive. The charge additives include ester- substituted and amide-substituted trianilino triazine materials. The webs prepared from the blends may be in the form of films or non-woven fibrous webs. Non-woven microfiber webs are useful as filtration media.

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24-09-2013 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US0008541438B2

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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21-06-2012 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: AU2005283085B2
Принадлежит:

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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09-01-2014 дата публикации

SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES

Номер: US20140011777A1
Принадлежит: 3M INNOVATIVE PROPERTIES COMPANY

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed. 2. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of in combination with a pharmaceutically acceptable carrier.3. The compound or salt of selected from the group consisting of:1-[(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol;1-[(4-amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol;1-[4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol;1-[(4-amino-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol;1-[4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol;1-{[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclobutanol;1-[(4-amino-2-hydroxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol; and1-{[4-amino-2-(2-hydroxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclobutanol.4. The compound or salt of selected from the group consisting of:1-[(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclohexanol;1-[(4-amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclohexanol;1-[(4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclohexanol;1-[(4-amino-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclohexanol;1-[(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclohexanol;1-{[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclohexanol;1-{[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclohexanol;1-{[4-amino-2-(hydroxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclohexanol;1-[2-(4-amino ...

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19-12-2003 дата публикации

Process for imidazo(4,5-c)pyridin-4-amines

Номер: AU2003233519A8
Принадлежит:

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19-12-2003 дата публикации

PROCESS FOR IMIDAZO(4,5-C)PYRIDIN-4-AMINES

Номер: AU2003233519A1
Принадлежит:

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29-10-2009 дата публикации

1-AMINO IMIDAZO-CONTAINING COMPOUNDS AND METHODS

Номер: US2009270443A1
Принадлежит:

Imidazo-containing compounds (e.g., imidazonaphthyridines, imidazopyridines) with an amino substituent at the 1-position, pharmaceutical compositions containing the compounds and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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11-05-2017 дата публикации

SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES

Номер: US20170129891A1
Принадлежит:

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed. 3. The compound or salt of wherein p is 0.4. The compound or salt of wherein m is 1.5. The compound or salt of wherein Z is selected from the group consisting of a bond and Calkylene.6. The compound or salt of wherein Z is —(CH)-A′—(CH)—.7. The compound or salt of wherein A′ is —O—.8. The compound or salt of wherein A′ is —N(R)— or —N(Q-R)—.9. The compound or salt of wherein Q is —S(O)— and Ris Calkyl.12. The compound or salt of wherein R′ is hydroxy.13. The compound or salt of wherein Ris hydrogen claim 2 , Calkyl claim 2 , HO—Calkylenyl claim 2 , or Calkyl-O—Calkylenyl.14. The compound or salt of claim 2 , wherein R′ is selected from the group consisting of —NHand —NH-Q-R claim 2 , wherein:{'sub': 2', '6', '8', '8', '1-4, 'Q is selected from the group consisting of —C(O)—, —C(O)—O—, —S(O)—, and —C(R)—N(R)—, wherein Ris selected from hydrogen and Calkyl; and'}{'sub': '4', 'Ris alkyl, aryl, arylalkylene, heteroaryl, and heterocyclyl, wherein the aryl group can be unsubstituted or substituted by acetylamino, alkyl, alkoxy, cyano, and halogen.'}15. The compound or salt of wherein:{'sub': 2', '4, 'claim-text': [{'sub': '1-2', 'X is Calkylene;'}, {'sub': 0-2', '2', '8', '6', '6', '6', '8', '6', '8', '6', '8', '6', '9, 'Y is selected from the group consisting of —S(O)—, —S(O)—N(R)—, —C(R)—, —C(R)—O—, —O—C(R)—, —O—C(O)—O—, —N(R)-Q-, —C(R)—N(R)—, —O—C(R)—N(R)—, and —C(R)—N(OR)—; and'}, {'sub': '4', 'Ris alkyl.'}], 'Ris selected from the group consisting of hydrogen, ...

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02-05-2006 дата публикации

Process for imidazo[4,5-c]pyridin-4-amines

Номер: US0007038053B2

A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine and converting a 7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine to a 1H-imidazo[4,5-c]pyridin-4-amine.

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10-09-2013 дата публикации

Electret webs with charge-enhancing additives

Номер: US0008529671B2

Electret webs are presented which include a blend of a thermoplastic resin and a charge additive. The charge additives include ester-substituted and amide-substituted trianilino triazine materials. The webs prepared from the blends may be in the form of films or non-woven fibrous webs. Non-woven microfiber webs are useful as filtration media.

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28-09-2005 дата публикации

Ether substituted imidazopyridines

Номер: CN0001674894A
Принадлежит:

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13-12-2007 дата публикации

Substituted Imidazoquinolines, Imidazopyridines, and Imidazonaphthyridines

Номер: US2007287724A1
Принадлежит:

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, 1,5-naphthyridines, 1,5-tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Подробнее
28-09-2004 дата публикации

Ether substituted imidazopyridines

Номер: US0006797718B2

Imidazopyridine compounds that contain an ether or thioether functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases. Methods of preparing the compounds and intermediates useful in the preparation of the compounds are also disclosed.

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24-10-2006 дата публикации

Ether substituted imidazopyridines

Номер: US0007125890B2

Imidazopyridine compounds that contain an ether or thioether functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases. Methods of preparing the compounds and intermediates useful in the preparation of the compounds are also disclosed.

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24-01-2017 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US0009550773B2

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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14-04-2015 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US0009006264B2

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Подробнее
13-09-2005 дата публикации

Process for imidazo[4,5-c]pyridin-4-amines

Номер: US0006943255B2

A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 7H-imidazo[4,5-c]tetrazolo[1,5-alpha]pyridine and converting a 7H-imidazo[4,5-c]tetrazolo[1,5-alpha]pyridine to a 1H-imidazo[4,5-c]pyridin-4-amine.

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08-02-2011 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US0007884207B2

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Подробнее
03-11-2005 дата публикации

Process for imidazo[4,5-c]pyridin-4-amines

Номер: US2005245516A1
Принадлежит:

A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine and converting a 7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine to a 1H-imidazo[4,5-c]pyridin-4-amine.

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22-05-2007 дата публикации

Ether substituted imidazopyridines

Номер: US0007220758B2

Imidazopyridine compounds that contain an ether or thioether functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases. Methods of preparing the compounds and intermediates useful in the preparation of the compounds are also disclosed.

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10-12-2009 дата публикации

METHOD FOR SUBSTITUTED IH-IMIDAZO[4,5-C] PYRIDINES

Номер: US2009306388A1
Принадлежит:

Methods for preparing compounds of the Formulas IV and I are disclosed. The methods include combining a compound of the Formula II: with a benzylamine of the Formula III: in the presence of an acid to provide a 1H-imidazo[4,5-c]pyridine compound of the Formula IV.

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15-12-2015 дата публикации

Method of making alpha, omega-diiodoperfluoroalkanes

Номер: US9212119B2

A method of making ,-diiodoperfluoroalkanes includes combining: diatomic iodine, at least one perfluoroalkylene oxide represented by the formula wherein Rf represents a perfluoroalkyl group; and at least one of: a) a first metallic compound comprising nickel, and a second metallic compound comprising molybdenum that is compositionally different from the first metallic compound; or b) a metallic alloy comprising from 50 to 70 percent by weight of nickel and from 20 to 40 percent by weight of molybdenum, based on the total weight of the metallic alloy, thereby producing at least one product represented by the formula I(CF2)nI, wherein n independently represents an integer in the range of from 1 to 11. The total weight of the at least one product wherein n is 3 or greater exceeds the total weight of the at least one product wherein n is 1 or 2 by a factor of at least 4.

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10-04-2018 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US0009938275B2

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Подробнее
24-11-2010 дата публикации

Electret webs with charge-enhancing additives

Номер: CN0101896657A
Принадлежит:

Electret webs are presented which include a blend of a thermoplastic resin and a charge additive. The charge additives include ester-substituted and amide-substituted trianilino triazine materials. The webs prepared from the blends may be in the form of films or non-woven fibrous webs. Non-woven microfiber webs are useful as filtration media.

Подробнее
06-08-2015 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US20150218162A1
Принадлежит: 3M Innovative Properties Co

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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09-08-2018 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: US20180222906A1
Принадлежит: 3M Innovative Properties Co

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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17-09-2015 дата публикации

METHOD OF MAKING ALPHA, OMEGA-DIIODOPERFLUOROALKANES

Номер: US20150259270A1
Принадлежит:

A method of making α,ω-diiodoperfluoroalkanes includes combining: diatomic iodine, at least one perfluoroalkylene oxide represented by the formula wherein Rrepresents a perfluoroalkyl group; and at least one of: a) a first metallic compound comprising nickel, and a second metallic compound comprising molybdenum that is compositionally different from the first metallic compound; or b) a metallic alloy comprising from 50 to 70 percent by weight of nickel and from 20 to 40 percent by weight of molybdenum, based on the total weight of the metallic alloy, thereby producing at least one product represented by the formula I(CF)I, wherein n independently represents an integer in the range of from 1 to 11. The total weight of the at least one product wherein n is 3 or greater exceeds the total weight of the at least one product wherein n is 1 or 2 by a factor of at least 4. 2. The method of claim 1 , wherein component iii) comprises both the first metallic compound and the second metallic compound.3. The method of claim 1 , wherein the first metallic compound comprises a powder.4. The method of claim 1 , wherein the second metallic compound further comprises nickel claim 1 , and wherein the weight ratio of the molybdenum to the nickel in the second metallic compound is at least 0.28.5. The method of claim 1 , wherein the second metallic compound further comprises nickel claim 1 , and wherein the weight ratio of the molybdenum to the nickel in the second metallic compound is at least 0.4.6. The method of claim 1 , wherein the molybdenum comprises at least 16 percent by weight of the second metallic compound.7. The method of claim 1 , wherein the method is carried out in a chemical reactor having an inner surface in contact with the components claim 1 , and wherein at least a portion of the inner surface comprises the first metallic compound or the second metallic compound.8. The method of claim 1 , wherein component iii) comprises the metallic alloy.9. The method of claim 8 , ...

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23-08-2007 дата публикации

Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines

Номер: WO2006028545A3

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Подробнее
01-09-2010 дата публикации

Electret webs with charge-enhancing additives

Номер: EP2222908A1
Принадлежит: 3M Innovative Properties Co

Electret webs are presented which include a blend of a thermoplastic resin and a charge additive. The charge additives include ester-substituted and amide-substituted trianilino triazine materials. The webs prepared from the blends may be in the form of films or non-woven fibrous webs. Non-woven microfiber webs are useful as filtration media.

Подробнее
11-12-2003 дата публикации

Process for imidazo[4,5-c]pyridin-4-amines

Номер: WO2003101949A2
Принадлежит: 3M INNOVATIVE PROPERTIES COMPANY

A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 4-phenoxy-1H-imidazo[4,5-c]pyridine and aminating the 4-phenoxy-1H-imidazo[4,5-c]pyridine to provide a 1H-imidazo[4,5-c]pyridin-4-amine.

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18-12-2003 дата публикации

Ether substituted imidazopyridines

Номер: CA2488801A1
Принадлежит: Individual

Imidazopyridine compounds that contain an ether functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases. Methods of preparing the compounds and intermediates useful in the preparation of the compounds are also disclosed.

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16-06-2005 дата публикации

PROCESS FOR IMIDAZO[4,5-c]PYRIDIN-4-AMINES

Номер: WO2004110991A3

A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine and converting a 7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridine to a 1H-imidazo[4,5-c]pyridin-4-amine.

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21-08-2008 дата публикации

Method for substituted 1h-imidazo[4,5-c]pyridines

Номер: WO2007092641A3

Methods for preparing compounds of the Formulas IV and I are disclosed. The methods include combining a compound of the Formula II: with a benzylamine of the Formula III: in the presence of an acid to provide a 1H-imidazo[4,5-c]pyridine compound of the Formula IV.

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18-04-2024 дата публикации

Stabilizing copolymer, adhesive composition, method of making the same, and article including the same

Номер: WO2024079569A1
Принадлежит: 3M INNOVATIVE PROPERTIES COMPANY

An adhesive composition comprises an acrylic copolymer having pendant organosiloxane groups, pendant polyether groups, and optionally acidic groups. An article comprises a substrate having the adhesive composition adhered thereto. A method of making the adhesive composition is also disclosed. Certain acrylic copolymers are disclosed.

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