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BR122017028096B8 - composto, composição farmacêutica, e, uso do composto - Google Patents

composto, composição farmacêutica, e, uso do composto

Info

Publication number
BR122017028096B8
BR122017028096B8 BR122017028096A BR122017028096A BR122017028096B8 BR 122017028096 B8 BR122017028096 B8 BR 122017028096B8 BR 122017028096 A BR122017028096 A BR 122017028096A BR 122017028096 A BR122017028096 A BR 122017028096A BR 122017028096 B8 BR122017028096 B8 BR 122017028096B8
Authority
BR
Brazil
Prior art keywords
group
compound
optionally substituted
optionally
nitrogen
Prior art date
Application number
BR122017028096A
Other languages
English (en)
Other versions
BR122017028096B1 (pt
Inventor
Hasuoka Atsushi
Nishida Haruyuki
Kajino Masahiro
Original Assignee
Takeda Pharmaceuticals Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37517870&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BR122017028096(B8) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda Pharmaceuticals Co filed Critical Takeda Pharmaceuticals Co
Publication of BR122017028096B1 publication Critical patent/BR122017028096B1/pt
Publication of BR122017028096B8 publication Critical patent/BR122017028096B8/pt

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/46Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
    • C07D207/48Sulfur 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
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • 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
    • 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pyrrole Compounds (AREA)

Abstract

a presente invenção fornece um composto tendo um efeito inibidor da secreção ácida superior e que mostra uma atividade anti-úlcera e outras. a presente invenção fornece um composto representado pela fórmula (i) em que r1 é um grupo heterocíclico monocíclico contendo nitrogênio opcionalmente condensado com um anel de benzeno ou um heterociclo, o grupo monocíclico heterocíclico contendo nitrogênio opcionalmente condensado com um anel de benzeno ou um heterociclo opcionalmente tem substituinte(s), r2 é um grupo arila c6-14 opcionalmente substituído, um grupo tienila opcionalmente substituído ou um grupo piridila opcionalmente substituído, r3 e r4 são cada um, um átomo de hidrogênio ou um de r3 e r4 é um átomo de hidrogênio e o outro é um grupo alquila inferior opcionalmente substituído, um grupo acila, um átomo de halogênio, um grupo ciano ou um grupo nitro, e r5 é um grupo alquila ou um sal deste.
BR122017028096A 2005-08-30 2006-08-29 composto, composição farmacêutica, e, uso do composto BR122017028096B8 (pt)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP2005250356 2005-08-30
JP2005-250356 2005-08-30
JP2006-100626 2006-03-31
JP2006100626 2006-03-31
BRPI0615111A BRPI0615111B8 (pt) 2005-08-30 2006-08-29 composto, composição farmacêutica, e, uso do composto
PCT/JP2006/317408 WO2007026916A1 (en) 2005-08-30 2006-08-29 1-heterocyclylsulfonyl, 2-aminomethyl, 5- (hetero-) aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors

Publications (2)

Publication Number Publication Date
BR122017028096B1 BR122017028096B1 (pt) 2021-04-13
BR122017028096B8 true BR122017028096B8 (pt) 2021-05-25

Family

ID=37517870

Family Applications (2)

Application Number Title Priority Date Filing Date
BRPI0615111A BRPI0615111B8 (pt) 2005-08-30 2006-08-29 composto, composição farmacêutica, e, uso do composto
BR122017028096A BR122017028096B8 (pt) 2005-08-30 2006-08-29 composto, composição farmacêutica, e, uso do composto

Family Applications Before (1)

Application Number Title Priority Date Filing Date
BRPI0615111A BRPI0615111B8 (pt) 2005-08-30 2006-08-29 composto, composição farmacêutica, e, uso do composto

Country Status (33)

Country Link
US (7) US7498337B2 (pt)
EP (2) EP1919865B1 (pt)
JP (3) JP4035559B1 (pt)
KR (2) KR101408561B1 (pt)
CN (1) CN101300229B (pt)
AR (1) AR055144A1 (pt)
AT (1) ATE504567T1 (pt)
AU (1) AU2006285641A1 (pt)
BR (2) BRPI0615111B8 (pt)
CA (1) CA2621182C (pt)
CR (1) CR9755A (pt)
CY (2) CY1111922T1 (pt)
DE (1) DE602006021195D1 (pt)
DK (2) DK1919865T3 (pt)
ES (2) ES2364498T3 (pt)
GE (1) GEP20105044B (pt)
HK (2) HK1118547A1 (pt)
HR (2) HRP20110473T1 (pt)
IL (1) IL189375A (pt)
JO (1) JO2791B1 (pt)
MA (1) MA29773B1 (pt)
ME (1) MEP10009A (pt)
NO (1) NO341894B1 (pt)
NZ (1) NZ566378A (pt)
PE (2) PE20110009A1 (pt)
PL (2) PL2327692T3 (pt)
PT (2) PT1919865E (pt)
RS (2) RS52473B9 (pt)
SI (2) SI1919865T1 (pt)
TW (1) TWI358296B (pt)
UA (1) UA94424C2 (pt)
WO (1) WO2007026916A1 (pt)
ZA (1) ZA200802488B (pt)

Families Citing this family (101)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007026916A1 (en) * 2005-08-30 2007-03-08 Takeda Pharmaceutical Company Limited 1-heterocyclylsulfonyl, 2-aminomethyl, 5- (hetero-) aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors
US8933105B2 (en) * 2007-02-28 2015-01-13 Takeda Pharmaceutical Company Limited Pyrrole compounds
JP5379690B2 (ja) 2007-09-28 2013-12-25 武田薬品工業株式会社 5員複素環化合物
KR101558011B1 (ko) * 2007-09-28 2015-10-06 다케다 야쿠힌 고교 가부시키가이샤 양성자 펌프 억제제로서의 5-원 이종원자고리 화합물
WO2009057784A1 (ja) 2007-11-01 2009-05-07 Takeda Pharmaceutical Company Limited 複素環化合物
GEP20146122B (en) * 2008-07-28 2014-07-25 Takeda Pharmaceuticals Co Pharmaceutical composition
WO2010021149A1 (ja) * 2008-08-21 2010-02-25 武田薬品工業株式会社 酸分泌抑制スピロ化合物
AR073136A1 (es) * 2008-08-27 2010-10-13 Takeda Pharmaceutical Compuestos de pirrol
EP3613734B1 (en) 2009-02-25 2021-08-25 Takeda Pharmaceutical Company Limited Process for producing pyrrole compound
AU2010228220B2 (en) 2009-03-26 2015-05-21 Takeda Pharmaceutical Company Limited Pyrazole compound
WO2011004882A1 (ja) * 2009-07-09 2011-01-13 ラクオリア創薬株式会社 消化管運動異常が関与する疾患を治療するためのアシッドポンプ拮抗剤
WO2012095691A1 (en) * 2011-01-15 2012-07-19 Jubilant Life Sciences Ltd. An improved process for producing aminopyridines
CN102863371B (zh) * 2011-07-06 2016-04-13 中国科学院上海有机化学研究所 氟代二氢吡咯或氟代吡咯
SG11201408511QA (en) * 2012-06-27 2015-01-29 Takeda Pharmaceutical Liquid preparations of amines and organic acids stabilized by salts
WO2014019442A1 (zh) * 2012-08-03 2014-02-06 上海恒瑞医药有限公司 苯并呋喃类衍生物、其制备方法及其在医药上的应用
US9388133B2 (en) 2012-11-19 2016-07-12 Jiangsu Hansoh Pharmaceutical Co., Ltd. Pyrrole sulfonamide derivative, preparation method for same, and medical application thereof
CN105143187B (zh) 2013-02-28 2018-04-03 武田药品工业株式会社 制备磺酰氯化合物的方法
KR102084185B1 (ko) * 2013-08-29 2020-03-04 주식회사 대웅제약 테트라히드로사이클로펜타피롤 유도체 및 이의 제조방법
KR102129842B1 (ko) 2013-10-02 2020-07-06 주식회사 대웅제약 술포닐인돌 유도체 및 이의 제조방법
CN103951652B (zh) * 2014-04-18 2015-09-23 潍坊博创国际生物医药研究院 5-(2-氟苯基)-n-甲基-1-(3-吡啶基磺酰基)-1h-吡咯-3-甲胺水溶性有机酸盐和注射剂及它们的制备方法
CN105367550A (zh) * 2014-08-11 2016-03-02 江苏柯菲平医药股份有限公司 四氢环戊二烯并[c]吡咯类衍生物、其制备方法及其在医药上的应用
CN105646451A (zh) * 2014-11-12 2016-06-08 江苏豪森药业集团有限公司 钾离子竞争性酸阻滞剂的晶型及其制备方法
CN104447490B (zh) * 2014-11-19 2017-06-06 连云港恒运医药有限公司 一种质子泵抑制剂的晶型、制备中间体及其合成方法和医药用途
CN104447491B (zh) * 2014-11-19 2017-06-23 连云港恒运医药有限公司 含吡咯环质子泵抑制剂的半富马酸盐及其中间体和医药用途
WO2016078594A1 (zh) * 2014-11-19 2016-05-26 江苏豪森药业集团有限公司 含吡咯环质子泵抑制剂的半富马酸盐及其晶型、中间体和医药用途
CN104356043B (zh) * 2014-11-27 2016-10-26 重庆威尔德浩瑞医药化工有限公司 一种制备5-(2-氟苯基)-1h-吡咯-3-甲醛的方法
CN105693693A (zh) * 2014-11-27 2016-06-22 江苏柯菲平医药股份有限公司 一种吡咯类胃酸分泌和抑制剂化合物盐的制备
CN105708812A (zh) * 2014-12-02 2016-06-29 江苏柯菲平医药股份有限公司 一种5-(2-氟苯基)-n-甲基-1-(3-吡啶基磺酰基)-1h-吡咯-3-甲氨冻干粉针及其制备方法
CN104860923B (zh) * 2015-01-21 2018-01-12 山东康美乐医药科技有限公司 富马酸沃诺拉赞的制备方法
CN105985278A (zh) * 2015-01-27 2016-10-05 江苏柯菲平医药股份有限公司 吡咯磺酰类衍生物、其制备方法及其在医药上的应用
CN105982867A (zh) * 2015-02-27 2016-10-05 江苏柯菲平医药股份有限公司 一种h009冻干粉针及其制备方法
CN106031710B (zh) * 2015-03-16 2019-03-12 南京优科制药有限公司 一种富马酸氟呐普拉赞的注射剂及其制备方法
CN104814964B (zh) * 2015-04-16 2018-07-31 广东赛烽医药科技有限公司 一种抗胃幽门螺旋杆菌的药物组合物、制备方法及其应用
KR101613245B1 (ko) 2015-04-27 2016-04-18 주식회사 대웅제약 신규의 4-메톡시 피롤 유도체 또는 이의 염 및 이를 포함하는 약학 조성물
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
CN104860926B (zh) * 2015-06-10 2017-06-30 浙江诚意药业股份有限公司 一种富马酸沃诺拉赞的制备方法
CN104945313A (zh) * 2015-06-19 2015-09-30 洪帅金 一种2-甲基-3-溴吡啶的制备方法
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KR102652511B1 (ko) 2015-06-30 2024-03-28 다케다 야쿠힌 고교 가부시키가이샤 피롤 화합물의 제조 방법
CN104974082A (zh) * 2015-07-26 2015-10-14 陈吉美 一种2-甲基-4-溴吡啶的制备方法
CN106432191A (zh) * 2015-08-10 2017-02-22 陕西合成药业股份有限公司 一种新的吡咯类衍生物、其制备方法及其在医药上的应用
CN105106203B (zh) * 2015-08-17 2019-04-05 江苏豪森药业集团有限公司 富马酸沃诺拉赞的药物组合物及其制备方法
CN105085484B (zh) * 2015-08-21 2017-11-24 南京济群医药科技股份有限公司 一种富马酸沃诺拉赞的制备方法
CN105030720B (zh) * 2015-08-26 2019-12-10 迪沙药业集团有限公司 一种富马酸沃诺拉赞肠溶片及其制备方法
CN105030725B (zh) * 2015-08-26 2019-12-10 迪沙药业集团有限公司 一种富马酸沃诺拉赞肠溶组合物及其制备方法
CN106478597A (zh) * 2015-09-02 2017-03-08 中美华世通生物医药科技(武汉)有限公司 富马酸沃诺拉赞单晶及其制备方法和用途
CN106511344A (zh) * 2015-09-14 2017-03-22 王虹 一种胃酸分泌抑制剂的新用途
CN106632246A (zh) * 2015-10-30 2017-05-10 江苏柯菲平医药股份有限公司 一种吡咯类胃酸分泌抑制剂化合物盐的晶型及其制备
CN105198802A (zh) * 2015-11-03 2015-12-30 江苏梦得电镀化学品有限公司 一种2-甲基-3-溴吡啶的制备方法
CN105294653B (zh) * 2015-11-16 2017-08-15 山东罗欣药业集团股份有限公司 富马酸沃诺拉赞的制备工艺
CN105440019A (zh) * 2015-12-17 2016-03-30 昆明贵研药业有限公司 一种治疗胃酸疾病药物的制备方法
CN105461690B (zh) * 2015-12-24 2018-07-24 南京济群医药科技股份有限公司 高纯度((5-(2-氟苯基)-1-(吡啶-3-基磺酰基)-1h-吡咯-3-基)甲基)(甲基)氨基甲酸叔丁酯的制备方法
CN105503828A (zh) * 2015-12-24 2016-04-20 北京康立生医药技术开发有限公司 一种吡咯衍生物的富马酸盐的制备方法
KR20170113040A (ko) * 2016-03-25 2017-10-12 주식회사 대웅제약 1-(5-(2,4-다이플루오로페닐)-1-((3-플루오로페닐)술포닐)-4-메톡시-1h-피롤-3-일)-n-메틸메탄아민의 신규한 산부가염
KR102081920B1 (ko) 2016-03-25 2020-02-26 주식회사 대웅제약 1-(5-(2,4-다이플루오로페닐)-1-((3-플루오로페닐)술포닐)-4-메톡시-1h-피롤-3-일)-n-메틸메탄아민 염의 신규한 결정형
CN106074406A (zh) * 2016-06-12 2016-11-09 佛山市腾瑞医药科技有限公司 一种富马酸沃诺拉赞分散片及其制备方法
CN108191830B (zh) * 2016-06-30 2019-06-14 珠海赛隆药业股份有限公司(长沙)医药研发中心 一种富马酸沃诺拉赞中间体ⅳ及其制备方法
KR101777971B1 (ko) 2016-07-05 2017-09-12 제일약품주식회사 이미다조[1,2-a]피리딘 유도체, 이의 제조방법 및 이의 용도
CN106187852B (zh) * 2016-07-07 2019-01-15 江西同和药业股份有限公司 一种富马酸沃诺拉赞中间体的制备方法
CN106431871A (zh) * 2016-08-17 2017-02-22 济南贝莱尔化学科技有限公司 一种2′‑溴代邻氟苯乙酮的制备方法
CN106243008B (zh) * 2016-08-22 2018-09-04 山东金城生物药业有限公司 富马酸沃诺拉赞中间体5-(2-氟苯基)-1h-吡咯-3-甲醛的制备方法
CN107778207A (zh) * 2016-08-25 2018-03-09 广东东阳光药业有限公司 富马酸沃诺拉赞中间体及其制备方法和用途
CN106397404A (zh) * 2016-08-31 2017-02-15 山东新华制药股份有限公司 5‑(2‑氟苯基)‑1‑(吡啶‑3‑基磺酰基)‑1h‑吡咯‑3‑甲醛的制备方法
CN106380464A (zh) * 2016-08-31 2017-02-08 山东新华制药股份有限公司 氟呐普拉赞关键中间体的制备方法
CN115385845B (zh) * 2016-09-12 2024-07-26 江苏柯菲平医药股份有限公司 一种吡咯磺酸类化合物盐型制备
CN107879964B (zh) * 2016-09-29 2023-02-10 江苏柯菲平医药股份有限公司 1-(5-(2-氟苯基)-1-(3-(3-甲氧丙氧基)苯磺酰氯)-1h-吡咯-3-基)-n-甲基胺的制备方法
CN108069891B (zh) * 2016-11-16 2022-09-20 江苏柯菲平医药股份有限公司 一类甲基甲胺盐酸盐的a晶型、制备及其应用
CN106892900A (zh) * 2017-04-10 2017-06-27 山东裕欣药业有限公司 一种富马酸沃诺拉赞及其制备方法
CN107011327A (zh) * 2017-04-19 2017-08-04 刘德鹏 一种治疗消化性溃疡的药物化合物及其制备方法
CN106905216A (zh) * 2017-04-19 2017-06-30 刘德鹏 一种质子泵抑制剂药物化合物及其制备方法
CN108794449B (zh) * 2017-05-05 2023-08-04 广东东阳光药业有限公司 一种氘代富马酸沃诺拉赞代谢物的合成方法
KR102233455B1 (ko) 2017-06-21 2021-03-29 주식회사 대웅제약 4-메톡시피롤 유도체의 중간체 제조 방법
PE20200442A1 (es) 2017-07-10 2020-02-28 Takeda Pharmaceuticals Co Preparacion que comprende vonoprazan
KR20190057569A (ko) 2017-11-20 2019-05-29 제일약품주식회사 7-아미노-1h-인돌-5-카르복사미드 유도체 및 이의 용도
KR102443292B1 (ko) * 2017-12-27 2022-09-14 닛뽕 케미파 가부시키가이샤 1-[5-(2-플루오로페닐)-1-(피리딘-3-일술포닐)-1h-피롤-3-일]-n-메틸메탄아민모노푸마르산염의 제조법
CN108558831B (zh) * 2018-06-08 2021-07-27 上海璃道医药科技有限公司 取代吡咯-4-烷基胺类化合物及其用途
CN109053684A (zh) * 2018-08-09 2018-12-21 珠海润都制药股份有限公司 一种富马酸沃诺拉赞及其中间体的制备方法
KR102126576B1 (ko) 2018-09-19 2020-06-24 주식회사 대웅제약 4-메톡시 피롤 유도체의 제조 방법
CN110272409A (zh) * 2019-03-11 2019-09-24 南京百迪尔生物医药有限公司 一步法合成沃诺拉赞的新方法
KR102222443B1 (ko) 2019-04-11 2021-03-03 일동제약(주) 1-[5-(2-플루오로페닐)-1-(피리딘-3-일술포닐)-1h-피롤-3-일]-n-메틸메탄아민의 신규염, 이의 제조방법 및 이를 포함하는 약제학적 조성물
CN112300123B (zh) * 2019-08-02 2023-07-18 上海天慈国际药业有限公司 一种沃诺拉赞中间体的制备方法
CN110627628A (zh) * 2019-09-24 2019-12-31 上海应用技术大学 一种β-碘代二氟丙酮类衍生物及其制备方法
CN112830920A (zh) * 2019-11-25 2021-05-25 杭州华东医药集团新药研究院有限公司 一种杂环衍生物、其药物组合物及用途
CN111018835B (zh) * 2019-12-16 2022-09-20 株洲千金药业股份有限公司 一种沃诺拉赞的纯化方法
CN113527536B (zh) * 2020-04-21 2024-03-22 杭州德柯医疗科技有限公司 一种含氟多糖高分子化合物及其制备方法
CN114349737B (zh) * 2020-04-26 2023-06-09 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应用、一种药物组合物及其应用
CN111484458B (zh) * 2020-05-25 2022-12-27 南京竹园医药科技有限公司 一种2-羟基-5-磺酸基嘧啶的制备方法
CN115884968B (zh) * 2020-06-17 2024-06-21 日东制药株式会社 新型酸分泌抑制剂及其用途
CN111943932B (zh) * 2020-08-06 2023-07-14 四川国康药业有限公司 一种可以治疗消化性溃疡的3-吡啶磺酰-1-n-杂吡咯衍生物及其制备方法和用途
CN114149411A (zh) * 2020-09-08 2022-03-08 鲁南制药集团股份有限公司 一种沃诺拉赞中间体及其制备方法与应用
CN112812099B (zh) * 2021-01-19 2022-04-26 珠海赛隆药业股份有限公司 一种用于治疗消化性溃疡的化合物及其制法和用途
CN114989138B (zh) * 2021-03-02 2023-06-13 天地恒一制药股份有限公司 沃诺拉赞盐及其晶型、制备方法和用途
CN115594622A (zh) * 2021-07-09 2023-01-13 天地恒一制药股份有限公司(Cn) 一种吡咯磺酰类衍生物、及其制备方法与应用
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
CN114105962B (zh) * 2021-10-26 2024-11-05 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
KR20230102353A (ko) * 2021-12-30 2023-07-07 주식회사 대웅제약 삼중음성유방암의 예방 또는 치료용 약학적 조성물
KR20230114147A (ko) 2022-01-24 2023-08-01 순천향대학교 산학협력단 칼륨 경쟁적 위산분비 억제제의 신규한 공결정, 이의 제조방법 및 이를 포함하는 약제학적 조성물
CN115232107A (zh) * 2022-07-29 2022-10-25 南京唯创远医药科技有限公司 一种高纯度富马酸伏诺拉生的制备方法
US12060148B2 (en) 2022-08-16 2024-08-13 Honeywell International Inc. Ground resonance detection and warning system and method
CN116023364A (zh) * 2023-01-31 2023-04-28 山东铂源药业股份有限公司 一种富马酸沃诺拉赞的制备方法
CN117462507B (zh) * 2023-12-28 2024-03-15 山东齐都药业有限公司 富马酸伏诺拉生药物组合物及其制备方法

Family Cites Families (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0259085B1 (en) 1986-08-29 1991-08-21 Pfizer Inc. 2-guanidino-4-arylthiazoles for treatment of peptic ulcers
US5128366A (en) 1990-07-05 1992-07-07 Shinogi & Co., Ltd. Pyrrole derivatives
AU8653891A (en) 1990-08-31 1992-03-30 Warner-Lambert Company Amino acid analogs as cck antagonists
CA2119155C (en) 1991-10-18 1999-06-15 Dennis Paul Phillion Fungicides for the control of take-all disease of plants
MX9205392A (es) 1991-10-29 1993-04-01 Du Pont Triazolcarbozamidas herbicidas y procedimiento para su obtencion.
JPH06135961A (ja) 1992-10-23 1994-05-17 Nippon Iyakuhin Kogyo Kk 新規ジフェニルピロリルフラン誘導体
US5286742A (en) * 1992-11-03 1994-02-15 American Cyanamid Company Pyrrole thiocarboxamide insecticidal and acaricidal agents
US5480902A (en) * 1993-08-31 1996-01-02 American Cyanamid Company Thienylpyrrole fungicidal agents
JPH08119936A (ja) 1994-10-18 1996-05-14 Fujisawa Pharmaceut Co Ltd 複素環式誘導体
JPH0930967A (ja) 1995-07-17 1997-02-04 Chugai Pharmaceut Co Ltd 抗潰瘍剤
DE69716449T2 (de) 1996-08-28 2003-08-07 The Procter & Gamble Company, Cincinnati Substituierte zyklische amine als metalloproteaseinhibitoren
IL130286A0 (en) 1996-12-23 2000-06-01 Du Pont Pharm Co Nitrogen containing heteroaromatics as factor Xa inhibitors
JPH11209344A (ja) 1998-01-26 1999-08-03 Kyowa Hakko Kogyo Co Ltd 含窒素複素環化合物
GB9817548D0 (en) * 1998-08-12 1998-10-07 Novartis Ag Organic compounds
ATE295831T1 (de) 1999-03-10 2005-06-15 Shionogi & Co Medizinische zubereitungen mit (2.2.1) und (3.1.1)bicycloskelett die antagonisten für sowohl pgd 2? als auch txa 2? rezeptoren sind
DE19913483A1 (de) 1999-03-25 2000-09-28 Goedecke Ag Verfahren zur Herstellung von Heterocyclischen Carbamaten aus Aza-Heterocyclen und Kohlendioxid
TW575561B (en) 1999-03-25 2004-02-11 Hoffmann La Roche 1-arenesulfonyl-2-aryl-pyrrolidine and piperidine derivatives
AU3783100A (en) 1999-06-14 2000-12-21 Dow Agrosciences Llc Substituted triazoles, imidazoles and pyrazoles as herbicides
ATE309995T1 (de) * 1999-08-26 2005-12-15 Aventis Pharma Inc Substituierte (aminoiminomethyl oder aminomethyl) dihydrobenzofurane und benozopyrane
AU2001258784A1 (en) 2000-05-22 2001-12-03 Takeda Chemical Industries Ltd. Tyrosine phosphatase inhibitors
US6589978B2 (en) 2000-06-30 2003-07-08 Hoffman-La Roche Inc. 1-sulfonyl pyrrolidine derivatives
GB0016453D0 (en) 2000-07-04 2000-08-23 Hoffmann La Roche Pyrrole derivatives
AU2002334733B2 (en) 2001-10-01 2006-11-23 Arena Pharmaceuticals, Inc. MCH receptors antagonists
US6919359B2 (en) 2001-11-08 2005-07-19 Pfizer Inc Azabicyclic-substituted-heteroaryl compounds for the treatment of disease
CA2464314A1 (en) 2001-11-22 2003-05-30 Ciba Specialty Chemicals Holding Inc. Pyrrole synthesis
WO2003057669A1 (fr) 2001-12-28 2003-07-17 Takeda Chemical Industries, Ltd. Antagonistes du recepteur androgene
AU2003216274A1 (en) 2002-02-11 2003-09-04 Neurocrine Biosciences, Inc. Pyrrole derivatives as ligands of melanocortin receptors
WO2003068740A1 (en) 2002-02-14 2003-08-21 Wyeth Pyrrolylalkylidene-hydrazinecarboximidamide derivatives as 5-hydroxytryptamine-6 ligands
TW200306191A (en) 2002-02-22 2003-11-16 Teijin Ltd Pyrrolopyrimidine derivatives
JP2006509720A (ja) * 2002-05-17 2006-03-23 メルクル・ゲーエムベーハー 潰瘍治療用プロトンポンプ阻害剤としての環付加ピロール化合物
EP1511733A2 (en) 2002-06-13 2005-03-09 E.I. Du Pont De Nemours And Company Pyrazole and pyrrole carboxamide insecticides
DE10228103A1 (de) 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
BR0313396A (pt) 2002-08-12 2005-06-28 Sugen Inc 3-pirrolil-piridopirazóis e 3-pirrolil-indazóis, como inibidores de quinase
JP2004315511A (ja) 2003-03-31 2004-11-11 Taisho Pharmaceut Co Ltd Mch受容体アンタゴニスト
EP1628957B1 (en) 2003-05-26 2010-09-29 Takeda Pharmaceutical Company Limited Sulfopyrroles
JP2005044740A (ja) 2003-07-25 2005-02-17 Taniguchi Heaters Kk 空焚きセンサー内蔵の液中用ヒーター
JP4239860B2 (ja) 2004-03-08 2009-03-18 ヤマハ株式会社 擦弦楽器用駒および擦弦楽器
RU2346996C2 (ru) 2004-06-29 2009-02-20 ЮРОПИЭН НИКЕЛЬ ПиЭлСи Усовершенствованное выщелачивание основных металлов
JP2006100626A (ja) 2004-09-30 2006-04-13 Fuji Photo Film Co Ltd 半導体発光装置
WO2006036024A1 (ja) * 2004-09-30 2006-04-06 Takeda Pharmaceutical Company Limited プロトンポンプ阻害薬
EP1655284A1 (en) 2004-10-26 2006-05-10 Aponetics AG 2-Phenylsulfopyrroles
WO2007026916A1 (en) * 2005-08-30 2007-03-08 Takeda Pharmaceutical Company Limited 1-heterocyclylsulfonyl, 2-aminomethyl, 5- (hetero-) aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors
KR101366856B1 (ko) * 2007-03-29 2014-02-21 삼성전자주식회사 다양한 포트를 통해 입력되는 영상을 디스플레이하는디스플레이 장치

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