JOP20220148A1 - عملية لانتاج استرات أسيلوكسي مثيل من حمض (4s)- (4-سيانو-2-ميثوكسي فنيل)-5-ايثوكسي-2، 8-ثنائي مثيل-1، 4-ثنائي هيدرو-1، 6-نفثيريدين-3-كربوكسيليك - Google Patents
عملية لانتاج استرات أسيلوكسي مثيل من حمض (4s)- (4-سيانو-2-ميثوكسي فنيل)-5-ايثوكسي-2، 8-ثنائي مثيل-1، 4-ثنائي هيدرو-1، 6-نفثيريدين-3-كربوكسيليكInfo
- Publication number
- JOP20220148A1 JOP20220148A1 JOP/2022/0148A JOP20220148A JOP20220148A1 JO P20220148 A1 JOP20220148 A1 JO P20220148A1 JO P20220148 A JOP20220148 A JO P20220148A JO P20220148 A1 JOP20220148 A1 JO P20220148A1
- Authority
- JO
- Jordan
- Prior art keywords
- producing
- naphthyridin
- methoxyphenyl
- dihydro
- ethoxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B57/00—Separation of optically-active compounds
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
- C12N9/18—Carboxylic ester hydrolases (3.1.1)
- C12N9/20—Triglyceride splitting, e.g. by means of lipase
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y301/00—Hydrolases acting on ester bonds (3.1)
- C12Y301/01—Carboxylic ester hydrolases (3.1.1)
- C12Y301/01003—Triacylglycerol lipase (3.1.1.3)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
يتعلق هذا الاختراع بعملية لانتاج استرات أسيلوكسي مثيل من حمض (4S)- (4-سيانو-2-ميثوكسي فنيل)-5-ايثوكسي-2، 8-ثنائي مثيل-1، 4-ثنائي هيدرو-1، 6-نفثيريدين-3-كربوكسيليك بالصيغة (IIa) عن طريق الاستبانة اللاتماثلية لمركب بالصيغة (II) باستخدام هيدرولاز. كما يتعلق هذا الاختراع بعملية لانتاج (4S)-4-(4-سيانو-2-ميثوكسي فنيل)-5-ايثوكسي-2، 8-ثنائي مثيل-1، 4-ثنائي هيدرو-1، 6-نفثيريدين-3-كربوكساميد بالصيغة (Ia) حيث تشتمل العملية على الاستبانة اللاتماثلية للمركب بالصيغة (II) باستخدام هيدرولاز. ويتعلق هذا الاختراع أيضاً باستخدام هيدرولاز في عملية لانتاج مركب بالصيغة (IIa). كما يتعلق هذا الاختراع أيضاً باستخدام هيدرولاز في عملية لانتاج مركب بالصيغة (Ia)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP19203821 | 2019-10-17 | ||
| PCT/EP2020/078611 WO2021074077A1 (de) | 2019-10-17 | 2020-10-12 | Verfahren zur herstellung von acyloxymethylestern der (4s) -(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridin-3-carbonsäure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JOP20220148A1 true JOP20220148A1 (ar) | 2023-01-30 |
Family
ID=68281309
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JOP/2022/0148A JOP20220148A1 (ar) | 2019-10-17 | 2020-10-12 | عملية لانتاج استرات أسيلوكسي مثيل من حمض (4s)- (4-سيانو-2-ميثوكسي فنيل)-5-ايثوكسي-2، 8-ثنائي مثيل-1، 4-ثنائي هيدرو-1، 6-نفثيريدين-3-كربوكسيليك |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US12365679B2 (ar) |
| EP (1) | EP4045500A1 (ar) |
| JP (1) | JP7757278B2 (ar) |
| KR (1) | KR20220084102A (ar) |
| CN (1) | CN114555599B (ar) |
| AU (1) | AU2020365314A1 (ar) |
| BR (1) | BR112022005605A2 (ar) |
| CA (1) | CA3157823A1 (ar) |
| CL (1) | CL2022000941A1 (ar) |
| CO (1) | CO2022004464A2 (ar) |
| CR (1) | CR20220161A (ar) |
| IL (1) | IL292194B1 (ar) |
| JO (1) | JOP20220148A1 (ar) |
| MX (1) | MX2022004480A (ar) |
| PE (1) | PE20221414A1 (ar) |
| WO (1) | WO2021074077A1 (ar) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4045499A1 (de) * | 2019-10-17 | 2022-08-24 | Bayer Aktiengesellschaft | Verfahren zur herstellung von 2-cyanoethyl (4s)-4-(4-cyano-2-methoxy-phenyl)-5-hydroxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridin-3-carboxylat durch racemat-spaltung mittels diastereomerer weinsäureester |
| CN114214375B (zh) * | 2021-12-27 | 2024-03-19 | 江苏威凯尔医药科技有限公司 | (r)-3-(4-卤代-1h-吡唑-1-基)-3-环戊基丙酸酯的制备方法 |
| CN115340539B (zh) * | 2022-01-19 | 2024-02-27 | 奥锐特药业股份有限公司 | 制备非奈利酮及其中间体的方法 |
| EP4511365A1 (en) | 2022-04-18 | 2025-02-26 | Teva Pharmaceuticals International GmbH | Processes for the preparation of finerenone |
| US20250115601A1 (en) * | 2022-05-16 | 2025-04-10 | Glenmark Life Sciences Limited | Process for the preparation of finerenone and intermediates thereof |
| CN115322194B (zh) * | 2022-08-23 | 2024-04-09 | 浙江国邦药业有限公司 | 一种非奈利酮中间体羧酸拆分方法 |
| CN121949317A (zh) * | 2023-01-12 | 2026-05-01 | 上海新礼泰药业有限公司 | 非奈利酮及其中间体的制备方法 |
| CN116218942B (zh) * | 2023-03-07 | 2025-07-25 | 常州制药厂有限公司 | 一种非奈利酮关键中间体及成品的制备方法 |
| CN116715664B (zh) * | 2023-06-12 | 2025-01-17 | 常州制药厂有限公司 | 一种非奈利酮关键中间体的制备方法 |
| CN117964619B (zh) * | 2024-01-30 | 2025-07-18 | 浙江神洲药业有限公司 | 一种非奈利酮及其制备方法以及非奈利酮中间体 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5234821A (en) * | 1990-09-01 | 1993-08-10 | Kazuo Achiwa | Process for preparing 1,4 dihydropyridine compounds |
| DE102007009494A1 (de) * | 2007-02-27 | 2008-08-28 | Bayer Healthcare Ag | Substituierte 4-Aryl-1, 4-dihydro-1,6-naphthyridinamide und ihre Verwendung |
| KR100848935B1 (ko) * | 2007-05-16 | 2008-07-29 | 주식회사 대희화학 | 생체 촉매 효소를 이용한 광학 선택적 가수분해방법 |
| CU20090172A7 (es) | 2009-10-09 | 2011-10-05 | Ct De Investigación Y Desarrollo De Medicamentos | Sistemas tricíclicos y tetracíclicos con actividad sobre el sistema nervioso central y vascular |
| ES2828704T3 (es) | 2014-08-01 | 2021-05-27 | Bayer Pharma AG | Procedimiento para la preparación de (4S)-4-(4-ciano-2-metoxifenil)-5-etoxi-2,8-dimetil-1,4-dihidro-1,6-naftiridin-3-carboxamida y su purificación para su uso como principio activo farmacéutico |
| RU2715226C2 (ru) * | 2015-08-21 | 2020-02-26 | Байер Фарма Акциенгезельшафт | Способ получения (4s)-4-(4-циано-2-метоксифенил)-5-этокси-2,8-диметил-1,4-дигидро-1,6-нафтиридин-3-карбоксамида и выделения (4s)-4-(4-циано-2-метоксифенил)-5-этокси-2,8-диметил-1,4-дигидро-1,6-нафтиридин-3-карбоксамида посредством электрохимических методов |
| RS59055B1 (sr) * | 2015-08-21 | 2019-08-30 | Bayer Pharma AG | Postupak za proizvodnju (4s)-4-(4-cijano-2-metoksifenil)-5-etoksi-2,8-dimetil-1,4-dihidro-1,6-naftiridin-3-karboksamida i njegovo prečišćavanje u svrhu upotrebe kao farmaceutski aktivne supstance |
| CN108473488A (zh) * | 2015-08-21 | 2018-08-31 | 拜耳制药股份公司 | (4s)-和(4r)-4-(4-氰基-2-甲氧基苯基)-5-乙氧基-2,8-二甲基-1,4-二氢-1,6-萘啶-3-甲酰胺的代谢物的制备方法及其用途 |
| CN106279000B (zh) | 2016-08-15 | 2019-06-18 | 哈尔滨商业大学 | 1,4-二氢-2,6-二甲基-4-(3-硝基苯基)-3,5-吡啶二羧酸单甲酯的制备方法 |
| CN108409731B (zh) * | 2018-03-07 | 2020-11-20 | 西华大学 | 芳基取代的1H-吡啶[3,4-b]吲哚-3-羧酸甲酯的手性拆分 |
-
2020
- 2020-10-12 JO JOP/2022/0148A patent/JOP20220148A1/ar unknown
- 2020-10-12 KR KR1020227015997A patent/KR20220084102A/ko active Pending
- 2020-10-12 PE PE2022000593A patent/PE20221414A1/es unknown
- 2020-10-12 CN CN202080072389.4A patent/CN114555599B/zh active Active
- 2020-10-12 WO PCT/EP2020/078611 patent/WO2021074077A1/de not_active Ceased
- 2020-10-12 CR CR20220161A patent/CR20220161A/es unknown
- 2020-10-12 CA CA3157823A patent/CA3157823A1/en active Pending
- 2020-10-12 EP EP20789970.9A patent/EP4045500A1/de active Pending
- 2020-10-12 BR BR112022005605A patent/BR112022005605A2/pt not_active Application Discontinuation
- 2020-10-12 US US17/769,241 patent/US12365679B2/en active Active
- 2020-10-12 MX MX2022004480A patent/MX2022004480A/es unknown
- 2020-10-12 IL IL292194A patent/IL292194B1/en unknown
- 2020-10-12 JP JP2022522986A patent/JP7757278B2/ja active Active
- 2020-10-12 AU AU2020365314A patent/AU2020365314A1/en active Pending
-
2022
- 2022-04-07 CO CONC2022/0004464A patent/CO2022004464A2/es unknown
- 2022-04-13 CL CL2022000941A patent/CL2022000941A1/es unknown
-
2025
- 2025-06-26 US US19/251,732 patent/US20250326751A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CN114555599A (zh) | 2022-05-27 |
| US12365679B2 (en) | 2025-07-22 |
| BR112022005605A2 (pt) | 2022-07-19 |
| CO2022004464A2 (es) | 2022-04-29 |
| CR20220161A (es) | 2022-06-17 |
| IL292194A (en) | 2022-06-01 |
| US20250326751A1 (en) | 2025-10-23 |
| US20240150344A1 (en) | 2024-05-09 |
| CL2022000941A1 (es) | 2022-11-11 |
| MX2022004480A (es) | 2022-05-06 |
| CA3157823A1 (en) | 2021-04-22 |
| WO2021074077A1 (de) | 2021-04-22 |
| KR20220084102A (ko) | 2022-06-21 |
| EP4045500A1 (de) | 2022-08-24 |
| PE20221414A1 (es) | 2022-09-20 |
| JP7757278B2 (ja) | 2025-10-21 |
| AU2020365314A1 (en) | 2022-05-12 |
| JP2022553225A (ja) | 2022-12-22 |
| CN114555599B (zh) | 2024-06-07 |
| IL292194B1 (en) | 2026-02-01 |
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