MX2022003401A - Compuesto de piridona fusionada y metodo de preparacion del mismo y uso del mismo. - Google Patents

Compuesto de piridona fusionada y metodo de preparacion del mismo y uso del mismo.

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Publication number
MX2022003401A
MX2022003401A MX2022003401A MX2022003401A MX2022003401A MX 2022003401 A MX2022003401 A MX 2022003401A MX 2022003401 A MX2022003401 A MX 2022003401A MX 2022003401 A MX2022003401 A MX 2022003401A MX 2022003401 A MX2022003401 A MX 2022003401A
Authority
MX
Mexico
Prior art keywords
preparation
method therefor
compound
pyridone compound
fused
Prior art date
Application number
MX2022003401A
Other languages
English (en)
Inventor
Haibing Guo
Yang Liu
Jianbiao Peng
Jun Fan
Shuchun Guo
Fang Bao
Original Assignee
Shanghai Jemincare Pharmaceuticals 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 Jemincare Pharmaceuticals Co Ltd filed Critical Shanghai Jemincare Pharmaceuticals Co Ltd
Publication of MX2022003401A publication Critical patent/MX2022003401A/es

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    • 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
    • C07D498/22Heterocyclic 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 four or more hetero rings
    • 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
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
    • A61K31/53831,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/22Heterocyclic 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 systems contains four or more hetero rings
    • 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
    • C07D498/12Heterocyclic 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 three hetero rings
    • C07D498/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/22Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

En la presente invención se describe un compuesto de piridona fusionada, y un método de preparación para este y un uso de este. Específicamente, la presente invención describe un compuesto de la fórmula (I-B), un isómero óptico del mismo y una sal farmacéuticamente aceptable del mismo, y el uso del compuesto como un inhibidor de KRAS. (ver fórmula).
MX2022003401A 2019-09-20 2020-09-21 Compuesto de piridona fusionada y metodo de preparacion del mismo y uso del mismo. MX2022003401A (es)

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
CN201910892032 2019-09-20
CN201911129688 2019-11-18
CN201911157939 2019-11-22
CN202010054188 2020-01-17
CN202010102546 2020-02-19
CN202010230303 2020-03-27
CN202010306926 2020-04-17
CN202010367694 2020-04-30
CN202010967317 2020-09-15
PCT/CN2020/116510 WO2021052499A1 (zh) 2019-09-20 2020-09-21 稠合吡啶酮类化合物及其制备方法和应用

Publications (1)

Publication Number Publication Date
MX2022003401A true MX2022003401A (es) 2022-07-13

Family

ID=74883935

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2022003401A MX2022003401A (es) 2019-09-20 2020-09-21 Compuesto de piridona fusionada y metodo de preparacion del mismo y uso del mismo.

Country Status (14)

Country Link
US (1) US20220389029A1 (es)
EP (1) EP4043464A4 (es)
JP (1) JP2022549171A (es)
KR (1) KR20220086573A (es)
CN (2) CN114728968A (es)
AU (1) AU2020350745A1 (es)
BR (1) BR112022005193A2 (es)
CA (1) CA3155066A1 (es)
CL (1) CL2022000666A1 (es)
CO (1) CO2022004686A2 (es)
IL (1) IL291467A (es)
MX (1) MX2022003401A (es)
TW (1) TWI761961B (es)
WO (1) WO2021052499A1 (es)

Families Citing this family (20)

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WO2019217307A1 (en) 2018-05-07 2019-11-14 Mirati Therapeutics, Inc. Kras g12c inhibitors
JP2022517222A (ja) 2019-01-10 2022-03-07 ミラティ セラピューティクス, インコーポレイテッド Kras g12c阻害剤
EP4021444A4 (en) 2019-08-29 2023-01-04 Mirati Therapeutics, Inc. G12D KRAS INHIBITORS
CN114761012A (zh) 2019-09-24 2022-07-15 米拉蒂治疗股份有限公司 组合疗法
KR20220106980A (ko) 2019-10-28 2022-08-01 머크 샤프 앤드 돔 코포레이션 Kras g12c 돌연변이체의 소분자 억제제
EP4053118A4 (en) * 2019-10-30 2023-01-04 Genfleet Therapeutics (Shanghai) Inc. SUBSTITUTED HETEROCYCLIC CONDENSED CYCLIC COMPOUND, METHOD FOR PREPARATION AND PHARMACEUTICAL USE
IL294048A (en) 2019-12-20 2022-08-01 Mirati Therapeutics Inc sos1 inhibitors
EP4129997A4 (en) * 2020-04-03 2024-01-24 Medshine Discovery Inc OCTAHYDROPYRAZINODIAZANAPHTHYRIDINDIONE COMPOUNDS
US20230295163A1 (en) * 2020-08-21 2023-09-21 Zhejiang Hisun Pharmaceutical Co., Ltd. Tetracyclic derivative, method for preparing same and use thereof in medicine
WO2022143995A1 (zh) * 2020-12-31 2022-07-07 正大天晴药业集团股份有限公司 四环类化合物及其医药用途
WO2022199669A1 (zh) * 2021-03-25 2022-09-29 上海济煜医药科技有限公司 稠合吡啶酮类化合物盐型、晶型及其应用
CN116848111A (zh) * 2021-03-26 2023-10-03 浙江海正药业股份有限公司 一种kras抑制剂关键中间体及其制备方法
CN115124533A (zh) * 2021-03-26 2022-09-30 浙江海正药业股份有限公司 四环类衍生物、其制备方法和其医药上的用途
CN116113632A (zh) * 2021-03-30 2023-05-12 浙江海正药业股份有限公司 杂环类衍生物、其制备方法及其医药上的用途
WO2022223037A1 (zh) * 2021-04-22 2022-10-27 劲方医药科技(上海)有限公司 Kras抑制剂的盐或多晶型物
AU2022314009A1 (en) * 2021-07-23 2024-01-25 Suzhou Zanrong Pharma Limited Kras g12d inhibitors and uses thereof
WO2023030517A1 (en) * 2021-09-06 2023-03-09 Suzhou Zanrong Pharma Limited Kras g12c inhibitors and uses thereof
TW202327593A (zh) * 2021-12-24 2023-07-16 大陸商勁方醫藥科技(上海)有限公司 Kras抑制劑的多晶型物及其製備方法和用途
CN116327956A (zh) * 2022-04-01 2023-06-27 劲方医药科技(上海)有限公司 药物组合物、其用途及癌症的治疗方法
WO2024081674A1 (en) 2022-10-11 2024-04-18 Aadi Bioscience, Inc. Combination therapies for the treatment of cancer

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EP3055290B1 (en) * 2013-10-10 2019-10-02 Araxes Pharma LLC Inhibitors of kras g12c
JO3556B1 (ar) * 2014-09-18 2020-07-05 Araxes Pharma Llc علاجات مدمجة لمعالجة السرطان
MX2017012979A (es) * 2015-04-10 2017-11-28 Araxes Pharma Llc Compuestos de quinazolina sustituidos y metodos de uso de los mismos.
JP6789239B2 (ja) * 2015-04-15 2020-11-25 アラクセス ファーマ エルエルシー Krasの縮合三環系インヒビターおよびその使用の方法
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US20200010479A1 (en) * 2017-02-03 2020-01-09 The University Of North Carolina At Chapel Hill Inhibitors of microbial beta-glucuronidase enzymes and uses thereof
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JOP20190272A1 (ar) * 2017-05-22 2019-11-21 Amgen Inc مثبطات kras g12c وطرق لاستخدامها
TW201938561A (zh) * 2017-12-08 2019-10-01 瑞典商阿斯特捷利康公司 化學化合物
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EP4053118A4 (en) * 2019-10-30 2023-01-04 Genfleet Therapeutics (Shanghai) Inc. SUBSTITUTED HETEROCYCLIC CONDENSED CYCLIC COMPOUND, METHOD FOR PREPARATION AND PHARMACEUTICAL USE

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Publication number Publication date
CA3155066A1 (en) 2021-03-25
IL291467A (en) 2022-05-01
JP2022549171A (ja) 2022-11-24
CN116947885A (zh) 2023-10-27
EP4043464A4 (en) 2023-10-04
EP4043464A1 (en) 2022-08-17
KR20220086573A (ko) 2022-06-23
TWI761961B (zh) 2022-04-21
CL2022000666A1 (es) 2022-10-14
WO2021052499A1 (zh) 2021-03-25
TW202126654A (zh) 2021-07-16
CN114728968A (zh) 2022-07-08
AU2020350745A1 (en) 2022-04-07
CO2022004686A2 (es) 2022-07-08
US20220389029A1 (en) 2022-12-08
BR112022005193A2 (pt) 2022-08-16

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