MX2022009765A - Preparacion de un antagonista del purinorreceptor 3 p2x (p2x3). - Google Patents

Preparacion de un antagonista del purinorreceptor 3 p2x (p2x3).

Info

Publication number
MX2022009765A
MX2022009765A MX2022009765A MX2022009765A MX2022009765A MX 2022009765 A MX2022009765 A MX 2022009765A MX 2022009765 A MX2022009765 A MX 2022009765A MX 2022009765 A MX2022009765 A MX 2022009765A MX 2022009765 A MX2022009765 A MX 2022009765A
Authority
MX
Mexico
Prior art keywords
antagonist
preparation
methyl
processes
methylcarbamol
Prior art date
Application number
MX2022009765A
Other languages
English (en)
Spanish (es)
Inventor
Nathalie Chauret
Jeremy Green
David R Kronenthal
Karine Villeneuve
Original Assignee
Bellus Health Cough Inc
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 Bellus Health Cough Inc filed Critical Bellus Health Cough Inc
Publication of MX2022009765A publication Critical patent/MX2022009765A/es

Links

Classifications

    • 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/40Esters thereof
    • C07F9/4003Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/4006Esters of acyclic acids which can have further substituents on alkyl
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
MX2022009765A 2020-02-14 2021-02-12 Preparacion de un antagonista del purinorreceptor 3 p2x (p2x3). MX2022009765A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202062977004P 2020-02-14 2020-02-14
US202163144902P 2021-02-02 2021-02-02
PCT/IB2021/000130 WO2021161109A1 (en) 2020-02-14 2021-02-12 Preparation of a p2x3 antagonist

Publications (1)

Publication Number Publication Date
MX2022009765A true MX2022009765A (es) 2022-09-09

Family

ID=77292130

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2022009765A MX2022009765A (es) 2020-02-14 2021-02-12 Preparacion de un antagonista del purinorreceptor 3 p2x (p2x3).

Country Status (11)

Country Link
US (1) US12503470B2 (https=)
EP (1) EP4103572A4 (https=)
JP (1) JP7693691B2 (https=)
KR (1) KR20220140804A (https=)
CN (1) CN115427419B (https=)
AU (1) AU2021219992A1 (https=)
BR (1) BR112022015818A2 (https=)
CA (1) CA3184277A1 (https=)
IL (1) IL295394A (https=)
MX (1) MX2022009765A (https=)
WO (1) WO2021161109A1 (https=)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7578602B2 (ja) 2019-02-25 2024-11-06 グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー3)、リミテッド P2x3修飾薬での治療
WO2022156783A1 (zh) * 2021-01-22 2022-07-28 武汉人福创新药物研发中心有限公司 咪唑并吡啶类化合物的制备方法及其中间体
CN114805237B (zh) * 2021-01-22 2026-04-21 武汉人福创新药物研发中心有限公司 杂环类化合物的制备方法及其中间体
WO2022161462A1 (zh) * 2021-01-29 2022-08-04 上海海雁医药科技有限公司 吗啉衍生物及其药物组合物和用途
WO2023021328A1 (en) * 2021-08-17 2023-02-23 Bellus Health Cough Inc. Preparation of a p2x3 antagonist
EP4577528A1 (en) * 2022-08-25 2025-07-02 14245563 Canada Inc. Preparation of a p2x3 antagonist
WO2025125445A1 (en) 2023-12-12 2025-06-19 Glaxosmithkline Intellectual Property (No.3) Limited Process of manufacture of p2x3 antagonists including camlipixant
WO2025191081A1 (en) 2024-03-15 2025-09-18 Glaxosmithkline Intellectual Property (No.3) Limited Crystalline form of camlipixant
WO2026022326A1 (en) 2024-07-25 2026-01-29 Glaxosmithkline Intellectual Property (No.3) Limited P2x3 antagonist formulation

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2010229142A1 (en) * 2009-03-23 2011-10-13 Merck Sharp & Dohme Corp. P2X3, receptor antagonists for treatment of pain
CN102358739B (zh) * 2011-04-29 2013-02-20 中国科学院广州生物医药与健康研究院 咪唑[1,2-a]吡啶和咪唑醛类化合物的合成方法
DK3381917T3 (da) * 2013-01-31 2021-10-18 Bellus Health Cough Inc Imidazopyridinforbindelser og anvendelser deraf
US10111883B1 (en) 2017-09-18 2018-10-30 Bellus Health Cough Inc. Selective P2X3 modulators
KR102797127B1 (ko) * 2018-12-29 2025-04-21 우한 크리에이터나 사이언스 앤드 테크놀로지 컴퍼니, 리미티드 헤테로고리계 화합물, 중간체, 이의 제조 방법 및 용도
EP4103564A4 (en) * 2020-02-14 2024-05-01 GlaxoSmithKline Intellectual Property (No.3) Limited P2X3 MODULATORS
WO2021244634A1 (zh) 2020-06-05 2021-12-09 武汉人福创新药物研发中心有限公司 咪唑并吡啶类化合物及其用途
EP4169921A4 (en) 2020-06-29 2024-06-19 Wuhan LL Science and Technology Development Co., Ltd. Crystalline form of heterocyclic compound, preparation method therefor and application thereof
WO2022156783A1 (zh) 2021-01-22 2022-07-28 武汉人福创新药物研发中心有限公司 咪唑并吡啶类化合物的制备方法及其中间体
CN114805237B (zh) 2021-01-22 2026-04-21 武汉人福创新药物研发中心有限公司 杂环类化合物的制备方法及其中间体

Also Published As

Publication number Publication date
JP7693691B2 (ja) 2025-06-17
IL295394A (en) 2022-10-01
BR112022015818A2 (pt) 2022-10-25
US20230101612A1 (en) 2023-03-30
JP2023513738A (ja) 2023-04-03
KR20220140804A (ko) 2022-10-18
CA3184277A1 (en) 2021-08-19
CN115427419A (zh) 2022-12-02
EP4103572A4 (en) 2024-03-06
WO2021161109A1 (en) 2021-08-19
CN115427419B (zh) 2026-04-21
EP4103572A1 (en) 2022-12-21
US12503470B2 (en) 2025-12-23
AU2021219992A1 (en) 2022-09-01

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