CN106604916A - 钾离子竞争性酸阻滞剂的晶型及其制备方法 - Google Patents

钾离子竞争性酸阻滞剂的晶型及其制备方法 Download PDF

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CN106604916A
CN106604916A CN201580047199.6A CN201580047199A CN106604916A CN 106604916 A CN106604916 A CN 106604916A CN 201580047199 A CN201580047199 A CN 201580047199A CN 106604916 A CN106604916 A CN 106604916A
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crystalline form
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solution
precipitate
ray powder
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CN106604916B (zh
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唐红伟
孙长安
王瑞军
袁恒立
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Jiangsu Hansoh Pharmaceutical Group Co Ltd
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    • 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
    • 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
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

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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)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

本发明涉及钾离子竞争性酸阻滞剂即1‑[5‑(2‑氟苯基)‑1‑(吡啶‑3‑基磺酰基)‑1H‑吡咯‑3‑基]‑N‑甲基甲胺富马酸盐(以下简称式I)的晶型及其制备方法,其X射线粉末衍射特征峰如附图1所示。本发明所提供的式I晶型性状稳定,可重复性好,适合药物开发。

Description

PCT国内申请,说明书已公开。

Claims (14)

  1. PCT国内申请,权利要求书已公开。
CN201580047199.6A 2014-11-12 2015-11-09 钾离子竞争性酸阻滞剂的晶型及其制备方法 Active CN106604916B (zh)

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CN201410637759.0A CN105646451A (zh) 2014-11-12 2014-11-12 钾离子竞争性酸阻滞剂的晶型及其制备方法
CN2014106377590 2014-11-12
PCT/CN2015/094120 WO2016074597A1 (zh) 2014-11-12 2015-11-09 钾离子竞争性酸阻滞剂的晶型及其制备方法

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US (1) US10538506B2 (zh)
EP (1) EP3219710B1 (zh)
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US9898175B2 (en) 2014-08-05 2018-02-20 Fibar Group S.A. Home network manager for home automation
CN105315258A (zh) * 2015-05-16 2016-02-10 南京海纳医药科技有限公司 富马酸沃诺拉赞多晶型及其制备方法
US10912769B2 (en) 2016-09-29 2021-02-09 Jiangsu Jibeier Pharmaceutical Co. Ltd. 1-[(pyridin-3-yl-sulfonyl)-1H-pyrrol-3-yl] methanamine derivative and pharmaceutical composition and use thereof
CN113620930B (zh) * 2021-07-12 2022-08-16 南京烁慧医药科技有限公司 一种含磺酰胺结构的化合物及其制备方法和应用、一种药物组合物及应用

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1803709A1 (en) * 2004-09-30 2007-07-04 Takeda Pharmaceutical Company Limited Proton pump inhibitors
CN101300229A (zh) * 2005-08-30 2008-11-05 武田药品工业株式会社 作为胃酸分泌抑制剂的1-杂环基磺酰基、2-氨基甲基、5-(杂)芳基取代的1-h-吡咯衍生物
WO2014133059A1 (ja) * 2013-02-28 2014-09-04 武田薬品工業株式会社 スルホニルクロライド化合物の製造法
CN104327051A (zh) * 2014-10-13 2015-02-04 成都盛迪医药有限公司 一种吡咯衍生物的富马酸盐的结晶形式

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6627646B2 (en) * 2001-07-17 2003-09-30 Sepracor Inc. Norastemizole polymorphs

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1803709A1 (en) * 2004-09-30 2007-07-04 Takeda Pharmaceutical Company Limited Proton pump inhibitors
CN101300229A (zh) * 2005-08-30 2008-11-05 武田药品工业株式会社 作为胃酸分泌抑制剂的1-杂环基磺酰基、2-氨基甲基、5-(杂)芳基取代的1-h-吡咯衍生物
WO2014133059A1 (ja) * 2013-02-28 2014-09-04 武田薬品工業株式会社 スルホニルクロライド化合物の製造法
CN104327051A (zh) * 2014-10-13 2015-02-04 成都盛迪医药有限公司 一种吡咯衍生物的富马酸盐的结晶形式

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WO2016074597A1 (zh) 2016-05-19
EP3219710A4 (en) 2018-05-09
US10538506B2 (en) 2020-01-21
TWI702211B (zh) 2020-08-21
TW201617336A (zh) 2016-05-16
CN106604916B (zh) 2020-03-03
EP3219710B1 (en) 2020-08-26
EP3219710A1 (en) 2017-09-20
US20180282300A1 (en) 2018-10-04
CN105646451A (zh) 2016-06-08

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