JP6854817B2 - Pi3k−ガンマ阻害薬としての複素環式化合物 - Google Patents
Pi3k−ガンマ阻害薬としての複素環式化合物 Download PDFInfo
- Publication number
- JP6854817B2 JP6854817B2 JP2018523015A JP2018523015A JP6854817B2 JP 6854817 B2 JP6854817 B2 JP 6854817B2 JP 2018523015 A JP2018523015 A JP 2018523015A JP 2018523015 A JP2018523015 A JP 2018523015A JP 6854817 B2 JP6854817 B2 JP 6854817B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- amino
- pyrazolo
- chloro
- carboxamide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CC*=C(*)C(*)=C(*)C*=*(C1N)[C@@]1(C1*)C1=C Chemical compound CC*=C(*)C(*)=C(*)C*=*(C1N)[C@@]1(C1*)C1=C 0.000 description 15
- FEGIMHQVLPQEGD-DMKDYFKLSA-N C/N=C\C(\c(nc(c(Cl)c1)C#N)c1C(OC)=O)=C/N Chemical compound C/N=C\C(\c(nc(c(Cl)c1)C#N)c1C(OC)=O)=C/N FEGIMHQVLPQEGD-DMKDYFKLSA-N 0.000 description 1
- IETMYICKLMTBEK-UHFFFAOYSA-N CC(c(cc(c1cnc[n]11)Cl)c1N(CCN1C)CC1=O)NC(Cc1c(NCC=C2)[n]2nc1N)=O Chemical compound CC(c(cc(c1cnc[n]11)Cl)c1N(CCN1C)CC1=O)NC(Cc1c(NCC=C2)[n]2nc1N)=O IETMYICKLMTBEK-UHFFFAOYSA-N 0.000 description 1
- YMCCNIOPQLOCFE-UHFFFAOYSA-N CC(c(cc1C)c(-c2ccccc2)[n]2c1c(C(F)(F)F)nc2C)=O Chemical compound CC(c(cc1C)c(-c2ccccc2)[n]2c1c(C(F)(F)F)nc2C)=O YMCCNIOPQLOCFE-UHFFFAOYSA-N 0.000 description 1
- XNVVPZBBXWZSSX-UHFFFAOYSA-N CC(c(cc1Cl)c(C2CCCCC2)[n]2c1cnc2)=O Chemical compound CC(c(cc1Cl)c(C2CCCCC2)[n]2c1cnc2)=O XNVVPZBBXWZSSX-UHFFFAOYSA-N 0.000 description 1
- UJDFHXXASSWZMU-UHFFFAOYSA-N CC(c1cc(N)c(C)c([N+]([O-])=O)c1OC(F)F)=O Chemical compound CC(c1cc(N)c(C)c([N+]([O-])=O)c1OC(F)F)=O UJDFHXXASSWZMU-UHFFFAOYSA-N 0.000 description 1
- HGDYONGBMAZAHS-UHFFFAOYSA-N CCOC(c1c(cccc2OC)[n]2nc1)=O Chemical compound CCOC(c1c(cccc2OC)[n]2nc1)=O HGDYONGBMAZAHS-UHFFFAOYSA-N 0.000 description 1
- YGJIBZHBUJQENT-MAAUZLAYSA-N CCOc1c(C#N)nc(/C(/C=N)=C/N)c(C(OC)=O)c1 Chemical compound CCOc1c(C#N)nc(/C(/C=N)=C/N)c(C(OC)=O)c1 YGJIBZHBUJQENT-MAAUZLAYSA-N 0.000 description 1
- LRDRDEWLQNUQEG-XFXZXTDPSA-N CN(C(C(C=C(/C1=C/N)O)=C(C2=CCCC=C2)N1N)=O)OC Chemical compound CN(C(C(C=C(/C1=C/N)O)=C(C2=CCCC=C2)N1N)=O)OC LRDRDEWLQNUQEG-XFXZXTDPSA-N 0.000 description 1
- CSYTZFVQPQUJLG-UHFFFAOYSA-N COC(c(cc1Cl)c(-c2cc(F)ccc2)nc1C#N)=O Chemical compound COC(c(cc1Cl)c(-c2cc(F)ccc2)nc1C#N)=O CSYTZFVQPQUJLG-UHFFFAOYSA-N 0.000 description 1
- YAZWIYPZVULADL-UHFFFAOYSA-N COC(c1c(N)nc2[n]1nc(C1C=NC=C(CO)C1)cc2)=O Chemical compound COC(c1c(N)nc2[n]1nc(C1C=NC=C(CO)C1)cc2)=O YAZWIYPZVULADL-UHFFFAOYSA-N 0.000 description 1
- QNKWCRPFGNCECQ-GJORDYMCSA-N C[C@@H]([C@H](C)/C(/O)=C/C(C)=O)C(C)=[NH+2] Chemical compound C[C@@H]([C@H](C)/C(/O)=C/C(C)=O)C(C)=[NH+2] QNKWCRPFGNCECQ-GJORDYMCSA-N 0.000 description 1
- GUQFVDKBVSOKAE-UHFFFAOYSA-N Cc1cnc(C)c(C(OC)=O)c1 Chemical compound Cc1cnc(C)c(C(OC)=O)c1 GUQFVDKBVSOKAE-UHFFFAOYSA-N 0.000 description 1
- BCCOTPMCAQSJLX-UHFFFAOYSA-N O=Cc(cc(c1cnc[n]11)Cl)c1N(CC1)CCS1(=O)=O Chemical compound O=Cc(cc(c1cnc[n]11)Cl)c1N(CC1)CCS1(=O)=O BCCOTPMCAQSJLX-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562252050P | 2015-11-06 | 2015-11-06 | |
| US62/252,050 | 2015-11-06 | ||
| PCT/US2016/060468 WO2017079519A1 (en) | 2015-11-06 | 2016-11-04 | Heterocyclic compounds as pi3k-gamma inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018532760A JP2018532760A (ja) | 2018-11-08 |
| JP2018532760A5 JP2018532760A5 (https=) | 2019-12-12 |
| JP6854817B2 true JP6854817B2 (ja) | 2021-04-07 |
Family
ID=57460598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018523015A Expired - Fee Related JP6854817B2 (ja) | 2015-11-06 | 2016-11-04 | Pi3k−ガンマ阻害薬としての複素環式化合物 |
Country Status (19)
| Country | Link |
|---|---|
| US (4) | US10065963B2 (https=) |
| EP (2) | EP4086259A1 (https=) |
| JP (1) | JP6854817B2 (https=) |
| AR (1) | AR106595A1 (https=) |
| CY (1) | CY1125245T1 (https=) |
| DK (1) | DK3371190T3 (https=) |
| ES (1) | ES2915550T3 (https=) |
| HR (1) | HRP20220599T1 (https=) |
| HU (1) | HUE059324T2 (https=) |
| LT (1) | LT3371190T (https=) |
| MA (1) | MA43169B1 (https=) |
| MD (1) | MD3371190T2 (https=) |
| PL (1) | PL3371190T3 (https=) |
| PT (1) | PT3371190T (https=) |
| RS (1) | RS63359B1 (https=) |
| SI (1) | SI3371190T1 (https=) |
| SM (1) | SMT202200250T1 (https=) |
| TW (2) | TWI744256B (https=) |
| WO (1) | WO2017079519A1 (https=) |
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| US20180185368A1 (en) | 2014-11-06 | 2018-07-05 | Lysosomal Therapeutics Inc. | Substituted pyrrolo[1,2-a]pyrimidines and their use in the treatment of medical disorders |
| US20170333435A1 (en) | 2014-11-06 | 2017-11-23 | Lysosomal Therapeutics Inc. | Substituted imidazo[1,5-a]pyrimidines and their use in the treatment of medical disorders |
| EP4406616A3 (en) | 2014-11-06 | 2024-11-06 | Bial-R&D Investments, S.A. | Substituted pyrazolo(1,5-a)pyrimidines and their use in the treatment of medical disorders |
| WO2016130501A1 (en) | 2015-02-09 | 2016-08-18 | Incyte Corporation | Aza-heteroaryl compounds as pi3k-gamma inhibitors |
| PT3371190T (pt) | 2015-11-06 | 2022-07-08 | Incyte Corp | Compostos heterocíclicos como inibidores de pi3k-gamma |
| US20170190689A1 (en) | 2016-01-05 | 2017-07-06 | Incyte Corporation | Pyridine and pyridimine compounds as pi3k-gamma inhibitors |
| AU2017222958B2 (en) * | 2016-02-25 | 2019-07-18 | Asceneuron S. A. | Glycosidase inhibitors |
| AU2017246455B2 (en) | 2016-04-06 | 2021-09-30 | Bial - R&D Investments, S.A. | Pyrazolo[1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| CA3020305A1 (en) | 2016-04-06 | 2017-10-12 | Lysosomal Therapeutics Inc. | Imidazo [1,5-a]pyrimidinyl carboxamide compounds and their use in the treatment of medical disorders |
| EP3440081A4 (en) | 2016-04-06 | 2019-09-18 | Lysosomal Therapeutics Inc. | PYRROLO [1,2-A] PYRIMIDINYL-CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDER |
| WO2017192931A1 (en) | 2016-05-05 | 2017-11-09 | Lysosomal Therapeutics Inc. | SUBSTITUTED IMDAZO[1,2-α]PYRIDINES, SUBSTITUTED IMIDAZO[1,2-α]PYRAZINES, RELATED COMPOUNDS, AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS |
| KR102530515B1 (ko) | 2016-05-05 | 2023-05-09 | 비알 - 알&디 인베스트먼츠, 에스.에이. | 치환된 이미다조[1,2-b]피리다진, 치환된 이미다조[1,5-b]피리다진, 관련 화합물, 및 의학적 장애의 치료에서의 그의 용도 |
| US10138248B2 (en) | 2016-06-24 | 2018-11-27 | Incyte Corporation | Substituted imidazo[2,1-f][1,2,4]triazines, substituted imidazo[1,2-a]pyridines, substituted imidazo[1,2-b]pyridazines and substituted imidazo[1,2-a]pyrazines as PI3K-γ inhibitors |
| TWI795381B (zh) | 2016-12-21 | 2023-03-11 | 比利時商健生藥品公司 | 作為malt1抑制劑之吡唑衍生物 |
| CN111182903A (zh) * | 2017-07-28 | 2020-05-19 | 特普医药公司 | 巨环化合物及其用途 |
| KR102717072B1 (ko) | 2017-10-18 | 2024-10-15 | 인사이트 코포레이션 | Pi3k-감마 저해제로서의 3차 하이드록시기로 치환된 축합된 이미다졸 유도체 |
| WO2019120212A1 (zh) * | 2017-12-19 | 2019-06-27 | 基石药业(苏州)有限公司 | Ido抑制剂 |
| CR20250050A (es) | 2018-09-05 | 2025-03-19 | Incyte Corp | Formas cristalinas de un inhibidor de fosfoinositida 3–quinasa (pi3k) (divisional 2021-0165) |
| CA3134814A1 (en) | 2019-03-26 | 2020-10-01 | Ventyx Biosciences, Inc. | Tyk2 pseudokinase ligands |
| EP3953345B1 (en) | 2019-04-11 | 2023-04-05 | Janssen Pharmaceutica NV | Pyridine rings containing derivatives as malt1 inhibitors |
| CN114206332B (zh) | 2019-06-04 | 2024-08-23 | 艾库斯生物科学有限公司 | 2,3,5-三取代吡唑并[1,5-a]嘧啶化合物 |
| AU2020289537A1 (en) | 2019-06-06 | 2021-11-25 | Aligos Therapeutics, Inc. | Heterocyclic compounds |
| JP7635228B2 (ja) | 2019-11-08 | 2025-02-25 | ベンティックス バイオサイエンシーズ,インク. | Tyk2偽キナーゼリガンド |
| CN116348453B (zh) * | 2021-04-25 | 2025-07-04 | 烨辉医药科技(上海)有限公司 | 杂芳族甲酰胺化合物及其用途 |
| WO2025146216A1 (zh) * | 2024-01-05 | 2025-07-10 | 成都赜灵生物医药科技有限公司 | 六并五氮杂环酰胺类化合物及其用途 |
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| TWI744256B (zh) | 2021-11-01 |
| SI3371190T1 (sl) | 2022-08-31 |
| US20200031837A1 (en) | 2020-01-30 |
| US20190062336A1 (en) | 2019-02-28 |
| US20170129899A1 (en) | 2017-05-11 |
| TWI824309B (zh) | 2023-12-01 |
| PL3371190T3 (pl) | 2022-11-07 |
| EP3371190A1 (en) | 2018-09-12 |
| DK3371190T3 (da) | 2022-05-23 |
| US10065963B2 (en) | 2018-09-04 |
| HRP20220599T1 (hr) | 2022-06-24 |
| US20230009843A1 (en) | 2023-01-12 |
| LT3371190T (lt) | 2022-08-10 |
| EP3371190B1 (en) | 2022-03-30 |
| ES2915550T3 (es) | 2022-06-23 |
| MA43169A (fr) | 2018-09-12 |
| JP2018532760A (ja) | 2018-11-08 |
| EP4086259A1 (en) | 2022-11-09 |
| CY1125245T1 (el) | 2025-03-28 |
| US11091491B2 (en) | 2021-08-17 |
| PT3371190T (pt) | 2022-07-08 |
| HUE059324T2 (hu) | 2022-11-28 |
| SMT202200250T1 (it) | 2022-07-21 |
| US11773102B2 (en) | 2023-10-03 |
| US10472368B2 (en) | 2019-11-12 |
| MD3371190T2 (ro) | 2022-09-30 |
| MA43169B1 (fr) | 2022-05-31 |
| WO2017079519A1 (en) | 2017-05-11 |
| TW201726679A (zh) | 2017-08-01 |
| TW202204362A (zh) | 2022-02-01 |
| AR106595A1 (es) | 2018-01-31 |
| RS63359B1 (sr) | 2022-07-29 |
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