TN2015000355A1 - Derives de pyrrolo [2, 3-d] pyrimidine servant d'inhibiteurs de kinases de type janus (jak) - Google Patents
Derives de pyrrolo [2, 3-d] pyrimidine servant d'inhibiteurs de kinases de type janus (jak)Info
- Publication number
- TN2015000355A1 TN2015000355A1 TN2015000355A TN2015000355A TN2015000355A1 TN 2015000355 A1 TN2015000355 A1 TN 2015000355A1 TN 2015000355 A TN2015000355 A TN 2015000355A TN 2015000355 A TN2015000355 A TN 2015000355A TN 2015000355 A1 TN2015000355 A1 TN 2015000355A1
- Authority
- TN
- Tunisia
- Prior art keywords
- jak
- pyrrolo
- kinase inhibitors
- janus
- pyrimidine derivatives
- Prior art date
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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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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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)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Pulmonology (AREA)
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- Biomedical Technology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Communicable Diseases (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
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Abstract
Il est décrit dans le présent mémoire des dérivés de pyrrolo (2,3 -d) pyramide, leur utilisation comme inhibiteurs de kinase janus (JAK) et des compositions pharmaceutiques les contenant
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 (1)
Publication Number | Publication Date |
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TN2015000355A1 true TN2015000355A1 (fr) | 2017-01-03 |
Family
ID=50151346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TN2015000355A TN2015000355A1 (fr) | 2013-02-22 | 2015-08-18 | Derives de pyrrolo [2, 3-d] pyrimidine servant d'inhibiteurs de kinases de type janus (jak) |
Country Status (47)
Families Citing this family (30)
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BR112013003631B1 (pt) | 2010-08-18 | 2021-10-13 | Samumed, Llc | Beta- e gama-dicetonas e gama-hidroxicetonas e composições farmacêuticas que as compreendem |
WO2014117035A1 (fr) | 2013-01-24 | 2014-07-31 | Transderm, Inc. | Compositions pour une administration transdermique d'inhibiteurs de mtor |
PL2968249T3 (pl) | 2013-02-22 | 2019-06-28 | Samumed, Llc | Gamma-diketony jako aktywatory szlaku sygnałowego Wnt/beta-kateniny |
ES2647525T3 (es) | 2013-02-22 | 2017-12-22 | Pfizer Inc. | Derivados de pirrolo[2,3-d]pirimidina como inhibidores de janus cinasas (JAK) |
JP6585158B2 (ja) * | 2014-08-12 | 2019-10-02 | ファイザー・インク | ヤヌスキナーゼの阻害に有用なピロロ[2,3−d]ピリミジン誘導体 |
HUE046741T2 (hu) | 2014-08-20 | 2020-03-30 | Samumed Llc | Gamma-diketonok bõröregedés és ráncok megelõzésére és kezelésére |
AU2016271904B2 (en) * | 2015-05-29 | 2018-05-10 | Wuxi Fortune Pharmaceutical Co.,Ltd | Janus kinase inhibitor |
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 |
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 |
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 |
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 |
CA3049402A1 (fr) | 2017-01-06 | 2018-07-12 | Palvella Therapeutics Llc | Compositions anhydres d'inhibiteurs de mtor et methodes d'utilisation |
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 |
HUE057970T2 (hu) | 2018-03-08 | 2022-06-28 | Incyte Corp | Aminopirazindiol-vegyületek mint PI3K-Y inhibitorok |
EP3817743A4 (fr) | 2018-07-02 | 2022-07-06 | Palvella Therapeutics, Inc. | Compositions anhydres d'inhibiteurs de mtor et méthodes d'utilisation |
US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
EP3817810A1 (fr) | 2018-07-06 | 2021-05-12 | Pfizer Inc. | Processus de fabrication et intermédiaires pour un composé de pyrrolo[2,3-d]pyrimidine et utilisation associée |
WO2020096948A1 (fr) * | 2018-11-05 | 2020-05-14 | Avista Pharma Solutions, Inc. | Composés chimiques |
KR20210120074A (ko) * | 2019-01-30 | 2021-10-06 | 가르가멜 (주하이) 바이오테크 리미티드 | Jak 억제제 및 그 제조 방법 |
AU2020222083B2 (en) | 2019-02-15 | 2022-11-17 | Pfizer Inc. | Crystalline pyrimidinyl-3,8-diazabicyclo(3.2.1)octanylmethanone compound and use thereof |
EP3939979A4 (fr) | 2019-03-14 | 2022-04-06 | Shanghai Synergy Pharmaceutical Sciences Co., Ltd | Inhibiteur de kinase jak, son procédé de préparation et ses applications dans le domaine de la médecine |
WO2020261041A1 (fr) * | 2019-06-27 | 2020-12-30 | Glenmark Life Sciences Limited | Procédé pour la préparation d'abrocitinib |
CA3153676A1 (fr) | 2019-09-11 | 2021-03-18 | Pfizer Inc. | Traitement de l'hidradenite avec des inhibiteurs de jak |
IL297050A (en) | 2020-04-04 | 2022-12-01 | Pfizer | Methods of treating the 2019 corona virus disease |
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 |
CA3184647A1 (fr) * | 2020-05-28 | 2021-12-02 | Pfizer Inc. | Derives de pyrrolo [2,3-d] pyrimidine |
AU2021341899A1 (en) * | 2020-09-11 | 2023-05-25 | Galderma Holding SA | Novel jak inhibitor compounds, method for synthesizing same and use thereof |
CN116847850A (zh) | 2021-02-02 | 2023-10-03 | 辉瑞公司 | 治疗慢性手部湿疹的给药方案 |
KR20230019801A (ko) * | 2021-08-02 | 2023-02-09 | 한국화학연구원 | 신규한 피롤로 피리미딘 유도체 화합물, 이의 제조방법, 및 이를 유효성분으로 포함하는 대사성 간질환의 예방 또는 치료용 약학적 조성물 |
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