HK1203499A1 - Pyrrolo[2,1-f][1,2,4]triazine compound, and preparation method and application thereof [21-f][124] - Google Patents

Pyrrolo[2,1-f][1,2,4]triazine compound, and preparation method and application thereof [21-f][124]

Info

Publication number
HK1203499A1
HK1203499A1 HK15104065.5A HK15104065A HK1203499A1 HK 1203499 A1 HK1203499 A1 HK 1203499A1 HK 15104065 A HK15104065 A HK 15104065A HK 1203499 A1 HK1203499 A1 HK 1203499A1
Authority
HK
Hong Kong
Prior art keywords
pyrrolo
preparation
application
triazine compound
triazine
Prior art date
Application number
HK15104065.5A
Other languages
English (en)
Chinese (zh)
Inventor
楊春皓
蒙凌華
陳艷紅
王祥
譚村
李家鵬
丁健
陳奕
Original Assignee
Shanghai Inst Materia Medica
Shanghai Haihe Pharmaceutical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shanghai Inst Materia Medica, Shanghai Haihe Pharmaceutical Co Ltd filed Critical Shanghai Inst Materia Medica
Publication of HK1203499A1 publication Critical patent/HK1203499A1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53861,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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
    • C07D498/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
HK15104065.5A 2012-05-31 2015-04-27 Pyrrolo[2,1-f][1,2,4]triazine compound, and preparation method and application thereof [21-f][124] HK1203499A1 (en)

Applications Claiming Priority (2)

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
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 (1)

Publication Number Publication Date
HK1203499A1 true HK1203499A1 (en) 2015-10-30

Family

ID=49672377

Family Applications (1)

Application Number Title Priority Date Filing Date
HK15104065.5A HK1203499A1 (en) 2012-05-31 2015-04-27 Pyrrolo[2,1-f][1,2,4]triazine compound, and preparation method and application thereof [21-f][124]

Country Status (14)

Country Link
US (1) US9447101B2 (es)
EP (1) EP2857403B1 (es)
JP (1) JP6067107B2 (es)
KR (1) KR101824299B1 (es)
CN (1) CN103450204B (es)
AU (1) AU2013270326B2 (es)
BR (1) BR112014029708B1 (es)
CA (1) CA2874062C (es)
ES (1) ES2703934T3 (es)
HK (1) HK1203499A1 (es)
MX (1) MX359207B (es)
RU (1) RU2589053C1 (es)
SG (1) SG11201407752YA (es)
WO (1) WO2013177983A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
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
WO2016064957A1 (en) 2014-10-22 2016-04-28 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
US10292985B2 (en) * 2015-08-31 2019-05-21 Bristol-Myers Squibb Company TGF beta receptor antagonists
CA3028822C (en) * 2016-06-25 2021-06-22 Suzhou Kintor Pharmaceuticals, Inc. Mechanistic target of rapamycin signaling pathway inhibitors and therapeutic applications thereof
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
CN111247150B (zh) * 2017-08-15 2022-11-08 石药集团中奇制药技术(石家庄)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)

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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
DE602005023333D1 (de) 2004-10-15 2010-10-14 Takeda Pharmaceutical Kinaseinhibitoren
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
EP2041138B1 (en) 2006-07-07 2014-06-25 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
US8022205B2 (en) * 2006-08-08 2011-09-20 Chugai Seiyaku Kabushiki Kaisha Pyrimidine derivatives as PI3K inhibitor and use thereof
PE20081679A1 (es) * 2006-12-07 2008-12-18 Hoffmann La Roche Compuestos del inhibidor de fosfoinositida 3-cinasa y metodos de uso
WO2008083398A2 (en) 2007-01-02 2008-07-10 Bristol-Myers Squibb Company Intermediate useful in preparing certain pyrrolotriazine compounds and a process for making the intermediate
JP5319659B2 (ja) 2007-04-18 2013-10-16 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
US8124759B2 (en) 2007-05-09 2012-02-28 Abbott Laboratories Inhibitors of protein kinases
US8129371B2 (en) * 2007-10-16 2012-03-06 Wyeth Llc Thienopyrimidine and pyrazolopyrimidine compounds and their use as mTOR kinase and PI3 kinase inhibitors
TW200938201A (en) * 2008-02-07 2009-09-16 Chugai Pharmaceutical Co Ltd Pyrrolopyrimidine derivative as PI3K inhibitor and 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
WO2010002472A1 (en) 2008-07-02 2010-01-07 Ambit Biosciences Corporation Jak kinase modulating compounds and methods of use thereof
EP2396315B1 (en) * 2009-02-13 2016-08-31 UCB Biopharma SPRL Quinoline derivatives as pi3k kinase inhibitors
EA022629B1 (ru) * 2009-04-16 2016-02-29 Фундасьон Сентро Насиональ Де Инвестигасьонес Онколохикас Карлос Iii Имидазопираны для применения в качестве ингибиторов киназ
WO2011089400A1 (en) * 2010-01-22 2011-07-28 Centro Nacional De Investigaciones Oncológicas (Cnio) Inhibitors of pi3 kinase
WO2011141713A1 (en) * 2010-05-13 2011-11-17 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

Also Published As

Publication number Publication date
CN103450204B (zh) 2016-08-17
EP2857403A4 (en) 2015-10-21
BR112014029708B1 (pt) 2023-05-02
CA2874062C (en) 2015-09-22
BR112014029708A2 (pt) 2017-06-27
SG11201407752YA (en) 2015-01-29
BR112014029708A8 (pt) 2021-09-08
MX359207B (es) 2018-09-19
EP2857403B1 (en) 2018-10-10
JP6067107B2 (ja) 2017-01-25
EP2857403A1 (en) 2015-04-08
MX2014014622A (es) 2015-08-10
AU2013270326A1 (en) 2014-12-18
RU2589053C1 (ru) 2016-07-10
ES2703934T3 (es) 2019-03-13
WO2013177983A1 (zh) 2013-12-05
KR101824299B1 (ko) 2018-03-14
AU2013270326B2 (en) 2016-07-14
US20150141644A1 (en) 2015-05-21
CA2874062A1 (en) 2013-12-05
CN103450204A (zh) 2013-12-18
KR20150009565A (ko) 2015-01-26
JP2015518010A (ja) 2015-06-25
US9447101B2 (en) 2016-09-20

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