CN115803316A - 吡啶酮类化合物及其制备方法和应用 - Google Patents

吡啶酮类化合物及其制备方法和应用 Download PDF

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Publication number
CN115803316A
CN115803316A CN202180049358.1A CN202180049358A CN115803316A CN 115803316 A CN115803316 A CN 115803316A CN 202180049358 A CN202180049358 A CN 202180049358A CN 115803316 A CN115803316 A CN 115803316A
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alkyl
compound
cancer
halogen
alkoxy
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程辉敏
温晓明
刘志强
张国刚
魏勇
齐珍珍
牛春意
张佩宇
赖力鹏
马健
温书豪
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Shenzhen Jingtai Technology Co Ltd
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Shenzhen Jingtai Technology Co Ltd
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    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/69Two or more oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

本发明公开一种吡啶酮类化合物及其制备方法及应用。具体地,本发明涉及式I化合物,其可用于治疗与肠易激综合征(IBS)和其他胃肠道障碍相关的疾病,以及治疗RET和/或TRK功能性障碍或调节RET和/或TRK活性的癌症、炎症性肠病、神经退行性疾病、慢性疼痛、急性疼痛、炎性疾病、克氏锥虫感染、与骨重建调节失衡有关的疾病。

Description

PCT国内申请,说明书已公开。

Claims (18)

  1. PCT国内申请,权利要求书已公开。
CN202180049358.1A 2020-07-23 2021-07-23 吡啶酮类化合物及其制备方法和应用 Pending CN115803316A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2020107197514 2020-07-23
CN202010719751 2020-07-23
PCT/CN2021/108286 WO2022017524A1 (zh) 2020-07-23 2021-07-23 吡啶酮类化合物及其制备方法和应用

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CN115803316A true CN115803316A (zh) 2023-03-14

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TW (1) TWI786742B (zh)
WO (1) WO2022017524A1 (zh)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105051027A (zh) * 2013-03-15 2015-11-11 葛兰素史密斯克莱知识产权发展有限公司 作为转染期间重排(ret)激酶抑制剂的吡啶衍生物
CN107001341A (zh) * 2014-10-16 2017-08-01 拜耳医药股份有限公司 含有磺亚胺基的氟化苯并呋喃基‑嘧啶衍生物
CN107074768A (zh) * 2014-09-10 2017-08-18 葛兰素史克知识产权发展有限公司 作为转染重排(ret)激酶抑制剂的吡啶酮衍生物
CN107250110A (zh) * 2014-09-10 2017-10-13 葛兰素史克知识产权发展有限公司 作为转染重排(ret)抑制剂的新化合物
CN111343987A (zh) * 2017-11-10 2020-06-26 安杰斯制药公司 作为trk激酶抑制剂之巨环化合物及其用途

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Publication number Priority date Publication date Assignee Title
PE20060664A1 (es) * 2004-09-15 2006-08-04 Novartis Ag Amidas biciclicas como inhibidores de cinasa
CA2587207A1 (en) * 2004-11-23 2006-06-01 Merck & Co., Inc. Niacin receptor agonists, compositions containing such compounds and methods of treatment
WO2009097972A1 (de) * 2008-02-05 2009-08-13 Sanofi-Aventis Sf5-derivate als par1-inhibitoren, ihre herstellung und verwendung als arzneimittel

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105051027A (zh) * 2013-03-15 2015-11-11 葛兰素史密斯克莱知识产权发展有限公司 作为转染期间重排(ret)激酶抑制剂的吡啶衍生物
CN107074768A (zh) * 2014-09-10 2017-08-18 葛兰素史克知识产权发展有限公司 作为转染重排(ret)激酶抑制剂的吡啶酮衍生物
CN107250110A (zh) * 2014-09-10 2017-10-13 葛兰素史克知识产权发展有限公司 作为转染重排(ret)抑制剂的新化合物
CN107001341A (zh) * 2014-10-16 2017-08-01 拜耳医药股份有限公司 含有磺亚胺基的氟化苯并呋喃基‑嘧啶衍生物
CN111343987A (zh) * 2017-11-10 2020-06-26 安杰斯制药公司 作为trk激酶抑制剂之巨环化合物及其用途

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Title
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JONATHAN D. MACDONALD ET AL.: "Discovery and Optimization of Salicylic Acid-Derived Sulfonamide Inhibitors of the WD Repeat-Containing Protein 5–MYC Protein–Protein Interaction", JOURNAL OF MEDICINAL CHEMISTRY, vol. 62, no. 24, 14 November 2019 (2019-11-14), pages 11232 - 11259, XP055888346, DOI: 10.1021/acs.jmedchem.9b01411 *
STEFANO ALTOMONTE ET AL.: "The pentafluorosulfanyl group in cannabinoid receptor ligands: synthesis and comparison with trifluoromethyl and tert-butyl analogues", RSC ADV., vol. 4, 15 April 2014 (2014-04-15), pages 20164 - 20176 *

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WO2022017524A1 (zh) 2022-01-27
TWI786742B (zh) 2022-12-11

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