AU2015276699B2 - Pyridino[1,2-a]pyrimidone analogue used as PI3K inhibitor - Google Patents
Pyridino[1,2-a]pyrimidone analogue used as PI3K inhibitor Download PDFInfo
- Publication number
- AU2015276699B2 AU2015276699B2 AU2015276699A AU2015276699A AU2015276699B2 AU 2015276699 B2 AU2015276699 B2 AU 2015276699B2 AU 2015276699 A AU2015276699 A AU 2015276699A AU 2015276699 A AU2015276699 A AU 2015276699A AU 2015276699 B2 AU2015276699 B2 AU 2015276699B2
- Authority
- AU
- Australia
- Prior art keywords
- group
- alkyl
- pharmaceutically acceptable
- compound
- reaction
- 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.)
- Active
Links
- 0 *C1CCCCC1 Chemical compound *C1CCCCC1 0.000 description 6
- RUBMBYZJQIWAFP-UHFFFAOYSA-N CC(NCCOC)=C Chemical compound CC(NCCOC)=C RUBMBYZJQIWAFP-UHFFFAOYSA-N 0.000 description 1
- UXZYDDQCFKCKLQ-UHFFFAOYSA-N CCCOC(C1=CN=C(C=CC(Br)=C2)N2C1=O)=O Chemical compound CCCOC(C1=CN=C(C=CC(Br)=C2)N2C1=O)=O UXZYDDQCFKCKLQ-UHFFFAOYSA-N 0.000 description 1
- DKPDGQQHSCKRFC-UHFFFAOYSA-N CCOC(C(C(OCC)=C)=CNc1ncc(C)cc1)=C Chemical compound CCOC(C(C(OCC)=C)=CNc1ncc(C)cc1)=C DKPDGQQHSCKRFC-UHFFFAOYSA-N 0.000 description 1
- TVCXVUHHCUYLGX-UHFFFAOYSA-N Cc1ccc[nH]1 Chemical compound Cc1ccc[nH]1 TVCXVUHHCUYLGX-UHFFFAOYSA-N 0.000 description 1
- WGOLHUGPTDEKCF-UHFFFAOYSA-N Nc(cc1)ncc1Br Chemical compound Nc(cc1)ncc1Br WGOLHUGPTDEKCF-UHFFFAOYSA-N 0.000 description 1
- PDQWZDOYLGXLAE-UHFFFAOYSA-N OCC1=CN=C(C=CC(Br)=C2)N2C1=O Chemical compound OCC1=CN=C(C=CC(Br)=C2)N2C1=O PDQWZDOYLGXLAE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410271282.9A CN105461711B (zh) | 2014-06-17 | 2014-06-17 | 作为PI3K抑制剂的吡啶并[1,2-a]嘧啶酮类似物 |
| CN201410271282.9 | 2014-06-17 | ||
| CN201510324348 | 2015-06-12 | ||
| CN201510324348.0 | 2015-06-12 | ||
| PCT/CN2015/081518 WO2015192760A1 (zh) | 2014-06-17 | 2015-06-16 | 作为pi3k抑制剂的吡啶并[1,2-a]嘧啶酮类似物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2015276699A1 AU2015276699A1 (en) | 2017-01-19 |
| AU2015276699B2 true AU2015276699B2 (en) | 2019-10-10 |
Family
ID=54934872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2015276699A Active AU2015276699B2 (en) | 2014-06-17 | 2015-06-16 | Pyridino[1,2-a]pyrimidone analogue used as PI3K inhibitor |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9856256B2 (enExample) |
| EP (1) | EP3159341B8 (enExample) |
| JP (1) | JP6680774B2 (enExample) |
| KR (1) | KR102495840B1 (enExample) |
| CN (1) | CN106470992B (enExample) |
| AU (1) | AU2015276699B2 (enExample) |
| CA (1) | CA2951971C (enExample) |
| EA (1) | EA032642B1 (enExample) |
| ES (1) | ES2754264T3 (enExample) |
| TW (1) | TWI628180B (enExample) |
| WO (1) | WO2015192760A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017101847A1 (zh) * | 2015-12-16 | 2017-06-22 | 正大天晴药业集团股份有限公司 | 吡啶并[1,2-a]嘧啶酮类似物、其晶型、其中间体及其制备方法 |
| CN110386932A (zh) | 2018-04-20 | 2019-10-29 | 艾科思莱德制药公司 | 用于抗肿瘤疗法中的双重atm和dna-pk抑制剂 |
| CN113316575B (zh) * | 2019-01-24 | 2022-03-18 | 江苏奥赛康药业有限公司 | 作为TGF-βR1激酶抑制剂的5-(4-吡啶氧基)吡唑类化合物 |
| BR112022010561A2 (pt) | 2019-12-02 | 2022-11-16 | Storm Therapeutics Ltd | Compostos poli-heterocíclicos como inibidores de mettl3 |
| US20230132982A1 (en) * | 2020-02-10 | 2023-05-04 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Use of pyrido[1,2-a]pyrimidinone compound in treating lymphoma |
| US20230119759A1 (en) | 2020-03-10 | 2023-04-20 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Pharmaceutical combination comprising pyridino[1,2-a]pyrimidinone compound |
| EP4197539A4 (en) * | 2020-09-15 | 2024-09-11 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Use of pyrido[1,2-a]pyrimidinone compound in treating peripheral t cell lymphoma |
| WO2022121929A1 (zh) * | 2020-12-08 | 2022-06-16 | 正大天晴药业集团股份有限公司 | 吡啶并[1,2-a]嘧啶酮化合物的治疗妇科肿瘤的用途 |
| WO2023169488A1 (zh) * | 2022-03-09 | 2023-09-14 | 正大天晴药业集团股份有限公司 | 包括吡啶并[1,2-a]嘧啶酮化合物和EGFR抑制剂的药物组合 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014022128A1 (en) * | 2012-07-29 | 2014-02-06 | Calitor Sciences, Llc | Pi3 kinase modulators and methods of use |
| WO2014110297A1 (en) * | 2013-01-09 | 2014-07-17 | Gilead Sciences, Inc. | (hetero) arylacetamide derivatives as antiretroviral agents |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7709473B2 (en) * | 2003-10-10 | 2010-05-04 | Pfizer Inc. | Substituted 2H-[1,2,4]triazolo[4,3-a]pyrazines as GSK-3 inhibitors |
| JP5642963B2 (ja) * | 2006-06-30 | 2014-12-17 | スネシス ファーマシューティカルズ,インコーポレイティド | ピリジノニルpdk1阻害剤 |
| EP2211615A4 (en) * | 2007-10-22 | 2010-10-13 | Glaxosmithkline Llc | PYRIDOSULFONAMIDE DERIVATIVES AS PI3 KINASE INHIBITORS |
| AU2009260447B2 (en) * | 2008-05-30 | 2012-03-29 | Amgen Inc. | Inhibitors of PI3 kinase |
| EA026385B9 (ru) * | 2010-07-02 | 2017-08-31 | Джилид Сайэнс, Инк. | Конденсированные гетероциклические соединения в качестве модуляторов ионных каналов |
| WO2012037108A1 (en) * | 2010-09-13 | 2012-03-22 | Glaxosmithkline Llc | Aminoquinoline derivatives as antiviral agents |
| US9284315B2 (en) * | 2011-11-17 | 2016-03-15 | Zuanzhu Pharma Co., Ltd. | Three-ring PI3K and/or mTOR inhibitor |
| CN103539777B (zh) * | 2012-07-13 | 2016-03-02 | 广东东阳光药业有限公司 | Pi3激酶调节剂及其使用方法和用途 |
| RU2658912C1 (ru) * | 2014-06-17 | 2018-06-26 | Шанхай Цзя Тань Фарматек Ко. Лтд. | АНАЛОГ ПИРИДИНО[1,2-А]ПИРИМИДОНА, ИСПОЛЬЗУЕМЫЙ В КАЧЕСТВЕ ИНГИБИТОРА mTOR/PI3K |
-
2015
- 2015-06-16 KR KR1020177000523A patent/KR102495840B1/ko active Active
- 2015-06-16 CN CN201580027396.1A patent/CN106470992B/zh active Active
- 2015-06-16 AU AU2015276699A patent/AU2015276699B2/en active Active
- 2015-06-16 EP EP15810067.7A patent/EP3159341B8/en active Active
- 2015-06-16 ES ES15810067T patent/ES2754264T3/es active Active
- 2015-06-16 JP JP2017518397A patent/JP6680774B2/ja active Active
- 2015-06-16 US US15/319,726 patent/US9856256B2/en active Active
- 2015-06-16 CA CA2951971A patent/CA2951971C/en active Active
- 2015-06-16 EA EA201790016A patent/EA032642B1/ru not_active IP Right Cessation
- 2015-06-16 WO PCT/CN2015/081518 patent/WO2015192760A1/zh not_active Ceased
- 2015-06-17 TW TW104119646A patent/TWI628180B/zh active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014022128A1 (en) * | 2012-07-29 | 2014-02-06 | Calitor Sciences, Llc | Pi3 kinase modulators and methods of use |
| WO2014110297A1 (en) * | 2013-01-09 | 2014-07-17 | Gilead Sciences, Inc. | (hetero) arylacetamide derivatives as antiretroviral agents |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2951971A1 (en) | 2015-12-23 |
| EA201790016A1 (ru) | 2017-06-30 |
| TWI628180B (zh) | 2018-07-01 |
| EP3159341B8 (en) | 2020-01-08 |
| JP2017519821A (ja) | 2017-07-20 |
| KR20170016465A (ko) | 2017-02-13 |
| US9856256B2 (en) | 2018-01-02 |
| US20170137420A1 (en) | 2017-05-18 |
| CA2951971C (en) | 2024-09-10 |
| EP3159341A1 (en) | 2017-04-26 |
| EA032642B1 (ru) | 2019-06-28 |
| EP3159341A4 (en) | 2018-05-16 |
| KR102495840B1 (ko) | 2023-02-03 |
| ES2754264T3 (es) | 2020-04-16 |
| AU2015276699A1 (en) | 2017-01-19 |
| CN106470992B (zh) | 2018-11-06 |
| EP3159341B1 (en) | 2019-08-21 |
| TW201625612A (zh) | 2016-07-16 |
| WO2015192760A1 (zh) | 2015-12-23 |
| JP6680774B2 (ja) | 2020-04-15 |
| CN106470992A (zh) | 2017-03-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) |