BR112014029708A2 - composto de pirrolo[2,1-f][1,2,4]triazina, método de preparação de compostos de pirrolo[2,1-f][1,2,4]triazina e uso do composto de pirrolo[2,1-f][1,2,4]triazina - Google Patents
composto de pirrolo[2,1-f][1,2,4]triazina, método de preparação de compostos de pirrolo[2,1-f][1,2,4]triazina e uso do composto de pirrolo[2,1-f][1,2,4]triazina Download PDFInfo
- Publication number
- BR112014029708A2 BR112014029708A2 BR112014029708A BR112014029708A BR112014029708A2 BR 112014029708 A2 BR112014029708 A2 BR 112014029708A2 BR 112014029708 A BR112014029708 A BR 112014029708A BR 112014029708 A BR112014029708 A BR 112014029708A BR 112014029708 A2 BR112014029708 A2 BR 112014029708A2
- Authority
- BR
- Brazil
- Prior art keywords
- pyrrolo
- triazine
- triazine compound
- preparing
- compound
- Prior art date
Links
- -1 pyrrolo [2,1-f] [1,2,4] triazine compound Chemical class 0.000 title abstract 6
- 238000000034 method Methods 0.000 title abstract 3
- KGRPHHFLPMPUBB-UHFFFAOYSA-N pyrrolo[2,1-f][1,2,4]triazine Chemical class C1=NC=NN2C=CC=C21 KGRPHHFLPMPUBB-UHFFFAOYSA-N 0.000 title abstract 3
- 108091007960 PI3Ks Proteins 0.000 abstract 2
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 abstract 2
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 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
- A61K31/535—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
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
-
- 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
- C07D498/08—Bridged 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
Abstract
resumo composto de pirrolo[2,1-f][1,2,4]triazina, método de preparação de compostos de pirrolo[2,1-f][1,2,4]triazina e uso do composto de pirrolo[2,1-f][1,2,4]triazina a presente invenção se refere a um composto de pirrolo[2,1-f][1,2,4]triazina, um isômero do mesmo ou um sal, éster ou hidrato farmaceuticamente aceitável do mesmo, e a um método de preparação e aplicação do mesmo. o composto de pirrolo[2,1-f][1,2,4]triazina tem uma estrutura expressa na fórmula geral (i). (i) o composto de pirrolo[2,1-f][1,2,4]triazina expresso na fórmula geral (i) pode inibir uma via de sinalização de fosfatidilinositol-3 quinase (p13k), sendo assim utilizado no preparo de medicamentos para tratar doenças relacionadas com fosfatidilinositol-3 quinase, tal como câncer. 1/1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210177980.3A CN103450204B (zh) | 2012-05-31 | 2012-05-31 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
CN201210177980.3 | 2012-05-31 | ||
PCT/CN2013/074559 WO2013177983A1 (zh) | 2012-05-31 | 2013-04-23 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
Publications (3)
Publication Number | Publication Date |
---|---|
BR112014029708A2 true BR112014029708A2 (pt) | 2017-06-27 |
BR112014029708A8 BR112014029708A8 (pt) | 2021-09-08 |
BR112014029708B1 BR112014029708B1 (pt) | 2023-05-02 |
Family
ID=49672377
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112014029708-8A BR112014029708B1 (pt) | 2012-05-31 | 2013-04-23 | Composto de pirrolo[2,1-f][1,2,4]triazina e método de preparação de compostos de pirrolo[2,1-f][1,2,4]triazina |
Country Status (14)
Country | Link |
---|---|
US (1) | US9447101B2 (pt) |
EP (1) | EP2857403B1 (pt) |
JP (1) | JP6067107B2 (pt) |
KR (1) | KR101824299B1 (pt) |
CN (1) | CN103450204B (pt) |
AU (1) | AU2013270326B2 (pt) |
BR (1) | BR112014029708B1 (pt) |
CA (1) | CA2874062C (pt) |
ES (1) | ES2703934T3 (pt) |
HK (1) | HK1203499A1 (pt) |
MX (1) | MX359207B (pt) |
RU (1) | RU2589053C1 (pt) |
SG (1) | SG11201407752YA (pt) |
WO (1) | WO2013177983A1 (pt) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9724352B2 (en) * | 2012-05-31 | 2017-08-08 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Pyrrolo[2,1-F[1,2,4]triazine compounds, preparation methods and applications thereof |
US9447105B2 (en) | 2013-01-24 | 2016-09-20 | Council Of Scientific & Industrial Research | Triazine compounds and a process for preparation thereof |
WO2016064958A1 (en) | 2014-10-22 | 2016-04-28 | Bristol-Myers Squibb Company | Heteroaryl substituted pyrrolotriazine amine compounds as pi3k inhibitors |
EP3209664B1 (en) | 2014-10-22 | 2020-06-03 | Bristol-Myers Squibb Company | Bicyclic heteroaryl amine compounds as pi3k inhibitors |
WO2017004134A1 (en) * | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
JP2018528951A (ja) * | 2015-08-31 | 2018-10-04 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | TGFβ受容体アンタゴニスト |
CN109641909B (zh) * | 2016-06-25 | 2022-01-11 | 苏州开拓药业股份有限公司 | 雷帕霉素信号通路抑制剂的机理靶标及其治疗应用 |
CN109111447A (zh) * | 2017-06-23 | 2019-01-01 | 中国科学院上海药物研究所 | 7-位取代吡咯并三嗪类化合物或其药学上可用的盐,及其制备方法和用途 |
WO2019034076A1 (zh) * | 2017-08-15 | 2019-02-21 | 南京明德新药研发股份有限公司 | Fgfr抑制剂及其医药用途 |
GB201720989D0 (en) * | 2017-12-15 | 2018-01-31 | Glaxosmithkline Ip Dev Ltd | Chemical compounds |
MX2022003217A (es) * | 2019-09-19 | 2022-06-29 | Totus Medicines Inc | Conjugados terapeuticos. |
CN112851563A (zh) * | 2020-12-30 | 2021-05-28 | 安徽金鼎医药股份有限公司 | N-氨基-3-氮杂双环[3,3,0]辛烷盐酸盐的合成工艺 |
WO2023035614A1 (zh) * | 2021-09-10 | 2023-03-16 | 上海海和药物研究开发股份有限公司 | 包含PI3Kα抑制剂的药物组合 |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6867300B2 (en) | 2000-11-17 | 2005-03-15 | Bristol-Myers Squibb Company | Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors |
TWI329112B (en) | 2002-07-19 | 2010-08-21 | Bristol Myers Squibb Co | Novel inhibitors of kinases |
TW200420565A (en) | 2002-12-13 | 2004-10-16 | Bristol Myers Squibb Co | C-6 modified indazolylpyrrolotriazines |
MY145634A (en) | 2003-12-29 | 2012-03-15 | Bristol Myers Squibb Co | Pyrrolotriazine compounds as kinase inhibitors |
US7713973B2 (en) | 2004-10-15 | 2010-05-11 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
US7151176B2 (en) | 2004-10-21 | 2006-12-19 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
TW200635927A (en) | 2004-12-22 | 2006-10-16 | Bristol Myers Squibb Co | Synthetic process |
US7232901B2 (en) | 2005-07-01 | 2007-06-19 | Bristol-Myers Squibb Company | Intermediates useful in preparing certain pyrrolotriazine compounds and process for making such intermediates |
US7514435B2 (en) | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
JP5185930B2 (ja) | 2006-07-07 | 2013-04-17 | ブリストル−マイヤーズ スクイブ カンパニー | ピロロトリアジンキナーゼ阻害剤 |
AU2007282535B9 (en) * | 2006-08-08 | 2013-06-20 | Chugai Seiyaku Kabushiki Kaisha | Pyrimidine derivative as PI3K inhibitor and use thereof |
US7888352B2 (en) * | 2006-12-07 | 2011-02-15 | Piramed Limited | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
US8148522B2 (en) | 2007-01-02 | 2012-04-03 | Bristol-Myers Squibb Company | Intermediate useful in preparing certain pyrrolotriazine compounds and a process for making the intermediate |
EP2134716A1 (en) | 2007-04-18 | 2009-12-23 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US8124759B2 (en) | 2007-05-09 | 2012-02-28 | Abbott Laboratories | Inhibitors of protein kinases |
MX2010004260A (es) * | 2007-10-16 | 2010-04-30 | Wyeth Llc | Compuestos de tienopirimidina y pirazolopirimidina y su uso como inhibidores de mtor cinasa y pi3 cinasa. |
CL2009000241A1 (es) * | 2008-02-07 | 2010-09-03 | Chugai Pharmaceutical Co Ltd | Compuestos derivados de 5-(2-morfolin-4-il-7h-pirrolo[2,3-d]pirimidin-4-il)pirimidin-2-ilamina; proceso de preparacion; composicion farmaceutica; y uso de los compuestos para tratar o prevenir una enfermedad proliferativa tal como el cancer. |
WO2010002472A1 (en) | 2008-07-02 | 2010-01-07 | Ambit Biosciences Corporation | Jak kinase modulating compounds and methods of use thereof |
WO2010002954A1 (en) * | 2008-07-02 | 2010-01-07 | Wyeth | (2-aryl-7h-pyrrolo[2,3-d]pyrimidin-4-yl)morpholine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
US8513284B2 (en) * | 2009-02-13 | 2013-08-20 | Ucb Pharma, S.A. | Fused pyridine and pyrazine derivatives as kinase inhibitors |
CA2756759C (en) * | 2009-04-16 | 2017-11-07 | Joaquin Pastor Fernandez | Imidazopyrazines for use as kinase inhibitors |
WO2011089400A1 (en) * | 2010-01-22 | 2011-07-28 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Inhibitors of pi3 kinase |
US20130131057A1 (en) * | 2010-05-13 | 2013-05-23 | Centro Nacional De Investigaciones Oncologicas (Cnio | New bicyclic compounds as pi3-k and mtor inhibitors |
CN102675323B (zh) * | 2012-06-01 | 2014-04-09 | 南京药石药物研发有限公司 | 吡咯并[2,1-f][1,2,4]三嗪衍生物及其抗肿瘤用途 |
-
2012
- 2012-05-31 CN CN201210177980.3A patent/CN103450204B/zh active Active
-
2013
- 2013-04-23 JP JP2015514329A patent/JP6067107B2/ja active Active
- 2013-04-23 AU AU2013270326A patent/AU2013270326B2/en active Active
- 2013-04-23 RU RU2014147863/04A patent/RU2589053C1/ru active
- 2013-04-23 ES ES13798006T patent/ES2703934T3/es active Active
- 2013-04-23 WO PCT/CN2013/074559 patent/WO2013177983A1/zh active Application Filing
- 2013-04-23 MX MX2014014622A patent/MX359207B/es active IP Right Grant
- 2013-04-23 CA CA2874062A patent/CA2874062C/en active Active
- 2013-04-23 EP EP13798006.6A patent/EP2857403B1/en active Active
- 2013-04-23 BR BR112014029708-8A patent/BR112014029708B1/pt active IP Right Grant
- 2013-04-23 KR KR1020147033824A patent/KR101824299B1/ko active IP Right Grant
- 2013-04-23 US US14/403,014 patent/US9447101B2/en active Active
- 2013-04-23 SG SG11201407752YA patent/SG11201407752YA/en unknown
-
2015
- 2015-04-27 HK HK15104065.5A patent/HK1203499A1/xx unknown
Also Published As
Publication number | Publication date |
---|---|
MX2014014622A (es) | 2015-08-10 |
CN103450204A (zh) | 2013-12-18 |
EP2857403A1 (en) | 2015-04-08 |
EP2857403A4 (en) | 2015-10-21 |
HK1203499A1 (en) | 2015-10-30 |
MX359207B (es) | 2018-09-19 |
BR112014029708A8 (pt) | 2021-09-08 |
RU2589053C1 (ru) | 2016-07-10 |
AU2013270326B2 (en) | 2016-07-14 |
BR112014029708B1 (pt) | 2023-05-02 |
CA2874062A1 (en) | 2013-12-05 |
JP6067107B2 (ja) | 2017-01-25 |
SG11201407752YA (en) | 2015-01-29 |
US9447101B2 (en) | 2016-09-20 |
CA2874062C (en) | 2015-09-22 |
JP2015518010A (ja) | 2015-06-25 |
KR101824299B1 (ko) | 2018-03-14 |
ES2703934T3 (es) | 2019-03-13 |
US20150141644A1 (en) | 2015-05-21 |
WO2013177983A1 (zh) | 2013-12-05 |
AU2013270326A1 (en) | 2014-12-18 |
EP2857403B1 (en) | 2018-10-10 |
CN103450204B (zh) | 2016-08-17 |
KR20150009565A (ko) | 2015-01-26 |
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B07D | Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette] | ||
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B06U | Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette] | ||
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B07A | Application suspended after technical examination (opinion) [chapter 7.1 patent gazette] | ||
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Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 23/04/2013, OBSERVADAS AS CONDICOES LEGAIS. PATENTE CONCEDIDA CONFORME ADI 5.529/DF, QUE DETERMINA A ALTERACAO DO PRAZO DE CONCESSAO. |
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B25A | Requested transfer of rights approved |
Owner name: SHANGHAI HAIHE PHARMACEUTICAL CO., LTD. (CN) |
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B25D | Requested change of name of applicant approved |
Owner name: HAIHE BIOPHARMA CO., LTD. (CN) |
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B25G | Requested change of headquarter approved |
Owner name: HAIHE BIOPHARMA CO., LTD. (CN) |