CU24275B1 - Derivados de cicloalquilo pirrolo [2,3-d] pirimidina-4-il amino útiles como inhibidores de quinasas janus relacionadas y composiciones farmacéuticas que contienen tales compuestos - Google Patents
Derivados de cicloalquilo pirrolo [2,3-d] pirimidina-4-il amino útiles como inhibidores de quinasas janus relacionadas y composiciones farmacéuticas que contienen tales compuestosInfo
- Publication number
- CU24275B1 CU24275B1 CUP2015000078A CU20150078A CU24275B1 CU 24275 B1 CU24275 B1 CU 24275B1 CU P2015000078 A CUP2015000078 A CU P2015000078A CU 20150078 A CU20150078 A CU 20150078A CU 24275 B1 CU24275 B1 CU 24275B1
- Authority
- CU
- Cuba
- Prior art keywords
- derivatives
- inhibitors
- cyclalquylcal
- pirimidina
- pirrolo
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D487/04—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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
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- Health & Medical Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
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- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pulmonology (AREA)
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- Neurosurgery (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361767947P | 2013-02-22 | 2013-02-22 | |
| PCT/IB2014/058889 WO2014128591A1 (fr) | 2013-02-22 | 2014-02-11 | Dérivés de pyrrolo[2,3-d]pyrimidine en tant qu'inhibiteurs de janus kinases (jak) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CU20150078A7 CU20150078A7 (es) | 2016-01-29 |
| CU24275B1 true CU24275B1 (es) | 2017-10-05 |
Family
ID=50151346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CUP2015000078A CU24275B1 (es) | 2013-02-22 | 2014-02-11 | Derivados de cicloalquilo pirrolo [2,3-d] pirimidina-4-il amino útiles como inhibidores de quinasas janus relacionadas y composiciones farmacéuticas que contienen tales compuestos |
Country Status (48)
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
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| MX354133B (es) | 2010-08-18 | 2018-02-14 | Samumed Llc | Dicetonas e hidroxicetonas como activadores de la trayectoria de señalizacion de catenina. |
| AU2014209141B2 (en) | 2013-01-24 | 2018-05-10 | Palvella Therapeutics, Inc. | Compositions for transdermal delivery of mTOR inhibitors |
| WO2014128591A1 (fr) | 2013-02-22 | 2014-08-28 | Pfizer Inc. | Dérivés de pyrrolo[2,3-d]pyrimidine en tant qu'inhibiteurs de janus kinases (jak) |
| EP3456325A3 (fr) | 2013-02-22 | 2019-05-22 | Samumed, LLC | Gamma-dicétones en tant qu'activateurs de la voie de signalisation wnt/ -caténine |
| WO2016024185A1 (fr) * | 2014-08-12 | 2016-02-18 | Pfizer Inc. | Dérivés de pyrrolo[2,3-d]pyrimidine utiles pour inhiber la janus kinase |
| SI3206686T1 (sl) | 2014-08-20 | 2020-03-31 | Samumed, Llc | Gama-diketoni za zdravljenje in preprečevanje staranja kože in gub |
| PL3305788T3 (pl) * | 2015-05-29 | 2021-03-08 | Wuxi Fortune Pharmaceutical Co., Ltd | Inhibitor kinazy janusowej |
| US11773106B2 (en) | 2015-10-16 | 2023-10-03 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US12365689B2 (en) | 2015-10-16 | 2025-07-22 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US11365198B2 (en) | 2015-10-16 | 2022-06-21 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| SG10201913989QA (en) | 2015-10-16 | 2020-03-30 | Abbvie Inc | PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-a]PYRROLO[2,3-e]-PYRAZIN-8-YL)-N-(2,2,2-TRIFLUOROETHYL)PYRROLIDINE-1-CARBOXAMIDE AND SOLID STATE FORMS THEREOF |
| US10550126B2 (en) | 2015-10-16 | 2020-02-04 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| CN106831779B (zh) * | 2015-11-28 | 2019-07-19 | 南昌弘益药业有限公司 | 一类jak激酶抑制剂的新化合物 |
| US10973913B2 (en) | 2016-02-16 | 2021-04-13 | Washington University | JAK inhibitors and uses thereof |
| CN110520097B (zh) | 2017-01-06 | 2023-10-27 | 帕尔维拉治疗股份有限公司 | Mtor抑制剂的无水组合物及其使用方法 |
| CN108794480A (zh) * | 2017-04-28 | 2018-11-13 | 天津药物研究院有限公司 | 吡咯并嘧啶类化合物、其制备方法和用途 |
| MD3762368T2 (ro) | 2018-03-08 | 2022-07-31 | Incyte Corp | Compuși diol aminopirazină ca inhibitori ai PI3K-Y |
| WO2020010003A1 (fr) | 2018-07-02 | 2020-01-09 | Incyte Corporation | DÉRIVÉS D'AMINOPYRAZINE UTILISÉS EN TANT QU'INHIBITEURS DE PI3K-γ |
| EP3817743A4 (fr) | 2018-07-02 | 2022-07-06 | Palvella Therapeutics, Inc. | Compositions anhydres d'inhibiteurs de mtor et méthodes d'utilisation |
| ES3045115T3 (en) | 2018-07-06 | 2025-11-27 | Pfizer | Manufacturing process and intermediates for a pyrrolo[2,3- d]pyrimidine compound and use thereof |
| BR112021008742A2 (pt) * | 2018-11-05 | 2021-08-10 | Avista Pharma Solutions, Inc. | compostos químicos |
| FI3915989T3 (fi) * | 2019-01-30 | 2023-09-20 | Felicamed Biotechnology Co Ltd | Jak:n estäjä ja sen valmistusmenetelmä |
| JP7561497B2 (ja) | 2019-02-15 | 2024-10-04 | ファイザー・インク | 結晶性ピリミジニル-3,8-ジアザビシクロ[3.2.1]オクタニルメタノン化合物およびその使用 |
| KR102737181B1 (ko) | 2019-03-14 | 2024-12-02 | 상하이 시너지 파마슈티컬 사이언시스 코., 엘티디. | Jak 억제제 및 그 제조방법과 의약분야에서의 응용 |
| WO2020261041A1 (fr) * | 2019-06-27 | 2020-12-30 | Glenmark Life Sciences Limited | Procédé pour la préparation d'abrocitinib |
| US12569487B2 (en) | 2019-09-11 | 2026-03-10 | Pfizer Inc. | Treatment of hidradenitis with jak inhibitors |
| WO2021062163A1 (fr) | 2019-09-27 | 2021-04-01 | Disc Medicine, Inc. | Procédés de traitement de la myélofibrose et d'affections associées |
| US20230149407A1 (en) | 2020-04-04 | 2023-05-18 | Pfizer Inc. | Methods of Treating Coronavirus Disease 2019 |
| CN113637018A (zh) | 2020-04-27 | 2021-11-12 | 苏州晶云药物科技股份有限公司 | 磺酰胺类化合物的晶型及其制备方法 |
| WO2021231798A1 (fr) | 2020-05-13 | 2021-11-18 | Disc Medicine, Inc. | Anticorps anti-hémojuvéline (hjv) pour le traitement de la myélofibrose |
| US20230219963A1 (en) * | 2020-05-28 | 2023-07-13 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine derivatives |
| CA3191607A1 (fr) * | 2020-09-08 | 2022-03-17 | Gilles Ouvry | Nouveaux composes inhibiteur de jak, leur procede de synthese et leur utilisation |
| AU2021341899A1 (en) * | 2020-09-11 | 2023-05-25 | Galderma Holding SA | Novel jak inhibitor compounds, method for synthesizing same and use thereof |
| EP4288058A1 (fr) | 2021-02-02 | 2023-12-13 | Pfizer Inc. | Régime posologique pour le traitement de l'eczéma de la main chronique |
| WO2023014049A1 (fr) * | 2021-08-02 | 2023-02-09 | 한국화학연구원 | Nouveau dérivé de pyrrolopyrimidine, son procédé de préparation et composition pharmaceutique le comprenant en tant que principe actif pour la prévention ou le traitement d'une maladie hépatique métabolique |
| CN118255769A (zh) * | 2022-12-28 | 2024-06-28 | 格格巫(珠海)生物科技有限公司 | 一种立体异构体的制备方法及中间体 |
| ES2993658B2 (es) | 2023-06-27 | 2025-07-02 | Moehs Iberica Sl | (3-(metil(7h-pirrolo[2,3-d]pirimidin-4-il)amino)ciclobutilo)carbamato de bencilo o una sal del mismo, procedimiento para su preparacion y su uso en la sintesis de abrocitinib |
| WO2025008772A2 (fr) | 2023-07-06 | 2025-01-09 | Pfizer Ireland Pharmaceuticals | Procédé de fabrication amélioré et intermédiaires pour un composé pyrrolo[2,3-d]pyrimidine et leur utilisation |
| ES3040374A1 (es) | 2024-04-30 | 2025-10-30 | Moehs Iberica Sl | Cocristales de N-{cis-3-[metil(7H-pirrolo[2,3-d]pirimidin-4-il)amino]ciclobutil}propano-1-sulfonamida |
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| JPH06329675A (ja) | 1993-05-20 | 1994-11-29 | Teijin Ltd | 4―置換アルキルアミノ―ピロロ[2,3―d]ピリミジン誘導体 |
| JPH06329674A (ja) | 1993-05-20 | 1994-11-29 | Teijin Ltd | 4―置換シクロヘキシルアミノ―ピロロ[2,3―d]ピリミジン |
| JPH08134068A (ja) | 1994-11-02 | 1996-05-28 | Teijin Ltd | 4―置換アルキルアミノ―ピロロ[2,3―d]ピリミジン誘導体 |
| US6051578A (en) | 1996-02-12 | 2000-04-18 | Pfizer Inc. | Pyrazolopyrimidines for treatment of CNS disorders |
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