HUS2200003I1 - Pirrolo [2,3-D]pirimidin származékok mint a Janus-kinázok (JAK) inhibitorai - Google Patents
Pirrolo [2,3-D]pirimidin származékok mint a Janus-kinázok (JAK) inhibitoraiInfo
- Publication number
- HUS2200003I1 HUS2200003I1 HUS2200003C HUS2200003C HUS2200003I1 HU S2200003 I1 HUS2200003 I1 HU S2200003I1 HU S2200003 C HUS2200003 C HU S2200003C HU S2200003 C HUS2200003 C HU S2200003C HU S2200003 I1 HUS2200003 I1 HU S2200003I1
- Authority
- HU
- Hungary
- Prior art keywords
- jak
- pyrrolo
- inhibitors
- pyrimidine derivatives
- janus kinases
- 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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- 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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- 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
- A61K31/535—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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- 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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- C—CHEMISTRY; METALLURGY
- 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
-
- 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)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Transplantation (AREA)
- Ophthalmology & Optometry (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
- Vascular Medicine (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361767947P | 2013-02-22 | 2013-02-22 | |
EP14705887.9A EP2958921B1 (en) | 2013-02-22 | 2014-02-11 | Pyrrolo [2, 3 -d]pyrimidine derivatives as inhibitors of janus kinases (jak) |
Publications (1)
Publication Number | Publication Date |
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HUS2200003I1 true HUS2200003I1 (hu) | 2022-02-28 |
Family
ID=50151346
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HUE17191163A HUE041778T2 (hu) | 2013-02-22 | 2014-02-11 | Pirrolo[2,3-d]pirimidin-származékok és egy vagy több további szer kombinációja Janus-típusú kinázok (JAK) gátlóiként |
HUE14705887A HUE037192T2 (hu) | 2013-02-22 | 2014-02-11 | Pirrolo [2,3-D]pirimidin származékok mint a Janus-kinázok (JAK) inhibitorai |
HUS2200003C HUS2200003I1 (hu) | 2013-02-22 | 2022-01-17 | Pirrolo [2,3-D]pirimidin származékok mint a Janus-kinázok (JAK) inhibitorai |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HUE17191163A HUE041778T2 (hu) | 2013-02-22 | 2014-02-11 | Pirrolo[2,3-d]pirimidin-származékok és egy vagy több további szer kombinációja Janus-típusú kinázok (JAK) gátlóiként |
HUE14705887A HUE037192T2 (hu) | 2013-02-22 | 2014-02-11 | Pirrolo [2,3-D]pirimidin származékok mint a Janus-kinázok (JAK) inhibitorai |
Country Status (47)
Families Citing this family (32)
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RU2016124136A (ru) | 2010-08-18 | 2018-12-03 | СЭМЬЮМЕД, ЭлЭлСи | Дикетоны и гидроксикетоны в качестве активатора сигнального пути катенина |
EP2948134B1 (en) | 2013-01-24 | 2020-03-04 | Palvella Therapeutics, Inc. | Compositions for transdermal delivery of mtor inhibitors |
RS58432B1 (sr) | 2013-02-22 | 2019-04-30 | Samumed Llc | Gama-diketoni kao aktivatori wnt/beta-kateninakog signalnog puta |
TR201902525T4 (tr) * | 2013-02-22 | 2019-03-21 | Pfizer | Janus ile alakalı kinazların (jak) inhibitörleri olarak bir veya daha fazla ilave ajan ile pirolo [2,3-d]pirimidin türevlerinin kombinasyonu. |
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 |
LT3206686T (lt) | 2014-08-20 | 2020-01-10 | Samumed, Llc | Gama-diketonai, skirti senėjančios odos ir raukšlių gydymui ir profilaktikai |
PT3305788T (pt) * | 2015-05-29 | 2020-09-25 | Wuxi Fortune Pharmaceutical Co Ltd | Inibidor da janus cinase |
SG10201913993QA (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 |
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 |
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 |
EP3565520A4 (en) | 2017-01-06 | 2020-08-19 | Palvella Therapeutics, Inc. | Anhydrous compositions of MTOR inhibitors and method of use |
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 |
UA128288C2 (uk) | 2018-03-08 | 2024-05-29 | Інсайт Корпорейшн | СПОЛУКИ АМІНОПІРАЗИНДІОЛУ ЯК ІНГІБІТОРИ PI3K-<font face="Symbol">g</font> |
JP2021530463A (ja) | 2018-07-02 | 2021-11-11 | パルヴェラ セラピューティクス、インク. | mTOR阻害剤の無水組成物および使用方法 |
US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
MX2020013896A (es) * | 2018-07-06 | 2021-03-09 | Pfizer | Proceso de fabricacion e intermediarios para un compuesto de pirrolo[2,3-d]pirimidina y su uso. |
EP3877389A4 (en) * | 2018-11-05 | 2022-07-13 | Avista Pharma Solutions, Inc. | CHEMICAL COMPOUNDS |
WO2020155931A1 (zh) * | 2019-01-30 | 2020-08-06 | 格格巫(珠海)生物科技有限公司 | 一种jak抑制剂及其制备方法 |
AU2020222083B2 (en) | 2019-02-15 | 2022-11-17 | Pfizer Inc. | Crystalline pyrimidinyl-3,8-diazabicyclo(3.2.1)octanylmethanone compound and use thereof |
KR20210134738A (ko) | 2019-03-14 | 2021-11-10 | 상하이 시너지 파마슈티컬 사이언시스 코., 엘티디. | Jak 억제제 및 그 제조방법과 의약분야에서의 응용 |
US20220259209A1 (en) * | 2019-06-27 | 2022-08-18 | Glenmark Life Sciences Limited | Process for the preparation of abrocitinib |
EP4028007A1 (en) * | 2019-09-11 | 2022-07-20 | Pfizer Inc. | Treatment of hidradenitis with jak inhibitors |
AU2021248720A1 (en) | 2020-04-04 | 2022-11-03 | 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 |
EP4157845A1 (en) * | 2020-05-28 | 2023-04-05 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine derivatives |
AU2021341899A1 (en) * | 2020-09-11 | 2023-05-25 | Galderma Holding SA | Novel jak inhibitor compounds, method for synthesizing same and use thereof |
MX2023008904A (es) | 2021-02-02 | 2023-08-09 | Pfizer | Regimen de dosificacion para el tratamiento del eczema cronico de manos. |
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 |
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 |
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