EA201891964A1 - СПОСОБ ПОЛУЧЕНИЯ МЕТИЛ{4,6-ДИАМИНО-2-[1-(2-ФТОРБЕНЗИЛ)-1H-ПИРАЗОЛО[3,4-b]ПИРИДИН-3-ИЛ]ПИРИМИДИН-5-ИЛ}МЕТИЛКАРБАМАТА И ЕГО ОЧИСТКИ ДЛЯ ПРИМЕНЕНИЯ В КАЧЕСТВЕ ФАРМАЦЕВТИЧЕСКОГО БИОЛОГИЧЕСКИ АКТИВНОГО ВЕЩЕСТВА - Google Patents
СПОСОБ ПОЛУЧЕНИЯ МЕТИЛ{4,6-ДИАМИНО-2-[1-(2-ФТОРБЕНЗИЛ)-1H-ПИРАЗОЛО[3,4-b]ПИРИДИН-3-ИЛ]ПИРИМИДИН-5-ИЛ}МЕТИЛКАРБАМАТА И ЕГО ОЧИСТКИ ДЛЯ ПРИМЕНЕНИЯ В КАЧЕСТВЕ ФАРМАЦЕВТИЧЕСКОГО БИОЛОГИЧЕСКИ АКТИВНОГО ВЕЩЕСТВАInfo
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- EA201891964A1 EA201891964A1 EA201891964A EA201891964A EA201891964A1 EA 201891964 A1 EA201891964 A1 EA 201891964A1 EA 201891964 A EA201891964 A EA 201891964A EA 201891964 A EA201891964 A EA 201891964A EA 201891964 A1 EA201891964 A1 EA 201891964A1
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- Eurasian Patent Office
- Prior art keywords
- diamino
- active substance
- pyrazoolo
- methylcarbammate
- methil
- Prior art date
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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Abstract
Настоящее изобретение касается способа получения метил{4,6-диамино-2-[1-(2-фторобензил)-1H-пиразоло[3,4-b]пиридин-3-ил]пиримидин-5-ил}метилкарбамата формулы (I)а также способа очистки исходного продукта соединения формулы (I) для применения в качестве фармацевтически активного вещества, причем для очистки метил{4,6-диамино-2-[1-(2-фторобензил)-1H-пиразоло[3,4-b]пиридин-3-ил]пиримидин-5-ил}метилкарбамат-сульфинилдиметана (1:1), т.е. в данном способе очистки соединение формулы (II)выделяют как промежуточную ступень или получают как промежуточную ступень, при необходимости в смеси.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP09177371 | 2009-11-27 |
Publications (2)
Publication Number | Publication Date |
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EA201891964A1 true EA201891964A1 (ru) | 2019-01-31 |
EA036422B1 EA036422B1 (ru) | 2020-11-09 |
Family
ID=43536603
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
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EA201891964A EA036422B1 (ru) | 2009-11-27 | 2010-11-22 | Способ получения метил-{4,6-диамино-2-[1-(2-фторбензил)-1h-пиразоло[3,4-b]пиридин-3-ил]пиримидин-5-ил}метилкарбамата |
EA201590948A EA031632B1 (ru) | 2009-11-27 | 2010-11-22 | СПОСОБ ПОЛУЧЕНИЯ МЕТИЛ{4,6-ДИАМИНО-2-[1-(2-ФТОРБЕНЗИЛ)-1H-ПИРАЗОЛО[3,4-b]ПИРИДИН-3-ИЛ]ПИРИМИДИН-5-ИЛ}МЕТИЛКАРБАМАТА |
EA201270636A EA022813B1 (ru) | 2009-11-27 | 2010-11-22 | СПОСОБ ОЧИСТКИ МЕТИЛ{4,6-ДИАМИНО-2-[1-(2-ФТОРБЕНЗИЛ)-1Н-ПИРАЗОЛО[3,4-b]ПИРИДИН-3-ИЛ]ПИРИМИДИН-5-ИЛ}МЕТИЛКАРБАМАТА И ЕГО ПРОИЗВОДНОЕ В ВИДЕ СУЛЬФИНИЛДИМЕТАНА |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
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EA201590948A EA031632B1 (ru) | 2009-11-27 | 2010-11-22 | СПОСОБ ПОЛУЧЕНИЯ МЕТИЛ{4,6-ДИАМИНО-2-[1-(2-ФТОРБЕНЗИЛ)-1H-ПИРАЗОЛО[3,4-b]ПИРИДИН-3-ИЛ]ПИРИМИДИН-5-ИЛ}МЕТИЛКАРБАМАТА |
EA201270636A EA022813B1 (ru) | 2009-11-27 | 2010-11-22 | СПОСОБ ОЧИСТКИ МЕТИЛ{4,6-ДИАМИНО-2-[1-(2-ФТОРБЕНЗИЛ)-1Н-ПИРАЗОЛО[3,4-b]ПИРИДИН-3-ИЛ]ПИРИМИДИН-5-ИЛ}МЕТИЛКАРБАМАТА И ЕГО ПРОИЗВОДНОЕ В ВИДЕ СУЛЬФИНИЛДИМЕТАНА |
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JP2013512252A (ja) | 2009-11-27 | 2013-04-11 | ジェンザイム・コーポレーション | グルコシルセラミドシンターゼの阻害剤としての非晶質及び結晶型のgenz112638ヘミ酒石酸塩 |
PE20180203A1 (es) * | 2009-11-27 | 2018-01-31 | Adverio Pharma Gmbh | Procedimiento para la preparacion de {4,6-diamino-2-[1-(2-fluorobencil)-1h-pirazolo[3,4-b]piridin-3-il]pirimidin-5-il}metilcarbamato de metilo y su purificacion para su uso como principio activo farmaceutico |
DE102010021637A1 (de) | 2010-05-26 | 2011-12-01 | Bayer Schering Pharma Aktiengesellschaft | Substituierte 5-Fluor-1H-Pyrazolopyridine und ihre Verwendung |
DE102010043379A1 (de) | 2010-11-04 | 2012-05-10 | Bayer Schering Pharma Aktiengesellschaft | Substituierte 6-Fluor-1H-Pyrazolo[4,3-b]pyridine und ihre Verwendung |
DE102010043380A1 (de) | 2010-11-04 | 2012-05-10 | Bayer Schering Pharma Aktiengesellschaft | Benzyl-substituierte Carbamate und ihre Verwendung |
UA111754C2 (uk) | 2011-10-06 | 2016-06-10 | Байєр Фарма Акцієнгезелльшафт | Заміщені бензиліндазоли для застосування як інгібіторів bub1-кінази для лікування гіперпроліферативних захворювань |
WO2013076168A1 (de) | 2011-11-25 | 2013-05-30 | Bayer Pharma Aktiengesellschaft | Verfahren zur herstellung von substituierten 5-fluor-1h-pyrazolopyridinen |
EA201500852A1 (ru) * | 2013-02-21 | 2016-02-29 | Адверио Фарма Гмбх | Формы метил {4,6-диамино-2-[1-(2-фторбензил)-1н-пиразоло[3,4-в]пиридино-3-ил]пиримидино-5-ил}метил карбамата |
CN104327107A (zh) * | 2013-10-17 | 2015-02-04 | 广东东阳光药业有限公司 | 一种氟喹诺酮类抗菌药物的制备方法 |
US10350206B2 (en) | 2014-09-19 | 2019-07-16 | Bayer Pharma Aktiengesellschaft | Benzyl substituted indazoles as BUB1 inhibitors |
WO2016113415A1 (en) | 2015-01-16 | 2016-07-21 | Sandoz Ag | Process for the preparation of riociguat essentially free from genotoxic impurities |
CN105367568B (zh) * | 2015-11-18 | 2019-08-20 | 浙江京新药业股份有限公司 | 一种制备利奥西呱的方法 |
CN105294686B (zh) * | 2015-11-30 | 2017-03-22 | 郑州大明药物科技有限公司 | 一种利奥西呱的制备方法 |
CN108463224A (zh) | 2015-12-14 | 2018-08-28 | 铁木医药有限公司 | sGC刺激剂用于胃肠功能障碍治疗的应用 |
WO2017103760A1 (en) * | 2015-12-15 | 2017-06-22 | Alembic Pharmaceuticals Limited | Novel polymorph of riociguat and its process for the preparation |
CN108069960A (zh) * | 2016-11-15 | 2018-05-25 | 江苏豪森药业集团有限公司 | 利奥西呱中间体的制备方法 |
WO2018096550A1 (en) * | 2016-11-28 | 2018-05-31 | Msn Laboratories Private Limited, R&D Center | Process for the preparation of methyl 4,6-diamino-2-[1-(2-fluorobenzyl)-1h-pyrazolo[3,4-b]pyridin-3-yl]-5-pyrimidinyl(methyl)carbamate and its polymorphs thereof |
WO2018111795A2 (en) | 2016-12-13 | 2018-06-21 | Ironwood Pharmaceuticals, Inc. | Use of sgc stimulators for the treatment of esophageal motility disorders |
WO2018130226A1 (zh) * | 2017-01-16 | 2018-07-19 | 苏州科睿思制药有限公司 | 利奥西呱的新晶型及其制备方法和用途 |
WO2020014504A1 (en) | 2018-07-11 | 2020-01-16 | Cyclerion Therapeutics, Inc. | USE OF sGC STIMULATORS FOR THE TREATMENT OF MITOCHONRIAL DISORDERS |
JP2023514532A (ja) * | 2020-02-03 | 2023-04-06 | アドヴェリオ・ファーマ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | メチル{4,6-ジアミノ-2-[5-フルオロ-1-(2-フルオロベンジル)-1H-ピラゾロ[3,4-b]ピリジン-3-イル]ピリミジン-5-イル}カルバメートのナノ製剤 |
CN111689961A (zh) * | 2020-06-01 | 2020-09-22 | 江苏华阳制药有限公司 | 一种利奧西呱的新晶型及其制备方法 |
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CN112316932B (zh) * | 2020-11-13 | 2022-03-01 | 中国石油大学(北京) | 一种粗对苯二甲酸加氢精制催化剂及其制备方法和应用 |
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