[go: up one dir, main page]

UA94424C2 - 1-heterocyclylsulfonyl, 2-aminomethyl, 5-(hetero-)aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors - Google Patents

1-heterocyclylsulfonyl, 2-aminomethyl, 5-(hetero-)aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors

Info

Publication number
UA94424C2
UA94424C2 UAA200803949A UAA200803949A UA94424C2 UA 94424 C2 UA94424 C2 UA 94424C2 UA A200803949 A UAA200803949 A UA A200803949A UA A200803949 A UAA200803949 A UA A200803949A UA 94424 C2 UA94424 C2 UA 94424C2
Authority
UA
Ukraine
Prior art keywords
group
ris
optionally substituted
acid secretion
optionally
Prior art date
Application number
UAA200803949A
Other languages
English (en)
Ukrainian (uk)
Inventor
Масахиро Каджино
Ацуши Хасуока
Харуюки Нишида
Original Assignee
Такеда Фармасьютикал Компани Лимитед
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=UA94424(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Такеда Фармасьютикал Компани Лимитед filed Critical Такеда Фармасьютикал Компани Лимитед
Publication of UA94424C2 publication Critical patent/UA94424C2/ru

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/46—Heterocyclic 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
    • C07D207/48—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/02—Heterocyclic 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
    • C07D417/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-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

Изобретение касается соединения, которое имеет чрезвычайную способность ингибировать секретирование кислоты и проявляет противоязвенную активность и т.д.Изобретение описывает соединение, представленное формулой (I), (I)где Rявляется азотосодержащей моноциклической гетероциклической группой, необязательно, конденсированной с бензольным кольцом или гетероциклом, азотосодержащей моноциклической гетероциклической группой, необязательно, конденсированной с бензольным кольцом или гетероциклом, который необязательно имеет заместитель(и), Rявляется необязательно замещенной Сарильной группой, необязательно замещенной тиенильной группой или необязательно замещенной пиридильной группой, Rи Rкаждый является атомом водорода, или один из Rи Rявляется атомом водорода и другой является необязательно замещенной низшей алкильной группой, ацильной группо�
UAA200803949A 2005-08-30 2006-08-29 1-heterocyclylsulfonyl, 2-aminomethyl, 5-(hetero-)aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors UA94424C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2005250356 2005-08-30
JP2006100626 2006-03-31

Publications (1)

Publication Number Publication Date
UA94424C2 true UA94424C2 (en) 2011-05-10

Family

ID=37517870

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA200803949A UA94424C2 (en) 2005-08-30 2006-08-29 1-heterocyclylsulfonyl, 2-aminomethyl, 5-(hetero-)aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors

Country Status (32)

Country Link
US (7) US7977488B2 (ru)
EP (2) EP2327692B9 (ru)
JP (3) JP4035559B1 (ru)
KR (2) KR101408561B1 (ru)
CN (1) CN101300229B (ru)
AR (1) AR055144A1 (ru)
AT (1) ATE504567T1 (ru)
AU (1) AU2006285641A1 (ru)
BR (2) BR122017028096B8 (ru)
CA (1) CA2621182C (ru)
CR (1) CR9755A (ru)
CY (2) CY1111922T1 (ru)
DE (1) DE602006021195D1 (ru)
DK (2) DK1919865T3 (ru)
ES (2) ES2391757T3 (ru)
GE (1) GEP20105044B (ru)
HR (2) HRP20110473T1 (ru)
IL (1) IL189375A (ru)
JO (1) JO2791B1 (ru)
MA (1) MA29773B1 (ru)
ME (1) ME00610B (ru)
NO (1) NO341894B1 (ru)
NZ (1) NZ566378A (ru)
PE (2) PE20070540A1 (ru)
PL (2) PL2327692T3 (ru)
PT (2) PT2327692E (ru)
RS (2) RS52473B9 (ru)
SI (2) SI2327692T1 (ru)
TW (1) TWI358296B (ru)
UA (1) UA94424C2 (ru)
WO (1) WO2007026916A1 (ru)
ZA (1) ZA200802488B (ru)

Families Citing this family (107)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE504567T1 (de) * 2005-08-30 2011-04-15 Takeda Pharmaceutical 1-heterocyclylsulfonyl, 2-aminomethyl, 5- (hetero-) aryl-substitutierte 1-h-pyrrolderivate als säuresekretionshemmer
US8933105B2 (en) * 2007-02-28 2015-01-13 Takeda Pharmaceutical Company Limited Pyrrole compounds
WO2009041705A2 (en) * 2007-09-28 2009-04-02 Takeda Pharmaceutical Company Limited 5-membered heterocyclic compounds as proton pump inhibitors
EP2196459B1 (en) 2007-09-28 2016-11-02 Takeda Pharmaceutical Company Limited 5-membered heterocyclic compound
JP5450083B2 (ja) 2007-11-01 2014-03-26 武田薬品工業株式会社 複素環化合物
EA201170272A1 (ru) * 2008-07-28 2011-10-31 Такеда Фармасьютикал Компани Лимитед Фармацевтическая композиция
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
ES2423289T3 (es) * 2008-08-27 2013-09-19 Takeda Pharmaceutical Company Limited Compuestos de pirrol
EP2765130B1 (en) * 2009-02-25 2017-07-26 Takeda Pharmaceutical Company Limited Intermediates for use in a process of producing pyrrole compounds
BRPI1009090A2 (pt) 2009-03-26 2016-03-01 Takeda Pharmaceutical composto, pró-droga, medicamento, métodos, e, uso do composto
JP5802898B2 (ja) * 2009-07-09 2015-11-04 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
CN110917130A (zh) * 2012-06-27 2020-03-27 武田药品工业株式会社 用盐稳定的胺和有机酸的液体制剂
CN104039776B (zh) * 2012-08-03 2016-06-08 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
KR20150084974A (ko) 2012-11-19 2015-07-22 장쑤 한서 파마슈티칼 캄파니 리미티드 피롤 설폰아미드 유도체, 이의 제조 방법, 및 이의 의학적 적용
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
CN106957252B (zh) * 2014-11-19 2019-11-19 连云港恒运药业有限公司 一种质子泵抑制剂中间体及其制备方法
CN107001262A (zh) * 2014-11-19 2017-08-01 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
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
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
CN104926790B (zh) * 2015-06-29 2017-07-07 江苏奥赛康药业股份有限公司 一种高纯度Vonoprazan Fumarate化合物及其中间体、杂质以及它们的制备方法
CA3229116A1 (en) 2015-06-30 2017-01-05 Takeda Pharmaceutical Company Limited Method for producing pyrrole compound
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
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
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
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
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
SG11202000136YA (en) * 2017-07-10 2020-02-27 Takeda Pharmaceuticals Co Preparation comprising 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
HUE070031T2 (hu) * 2020-06-17 2025-05-28 Ildong Pharmaceutical Co Ltd Új savszekréciós inhibitor és alkalmazása
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
CN114149411B (zh) * 2020-09-08 2025-05-16 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
CN116239606B (zh) * 2021-07-09 2025-09-02 天地恒一制药股份有限公司 一种吡咯磺酰类衍生物、及其制备方法与应用
CN115594622B (zh) * 2021-07-09 2025-03-21 天地恒一制药股份有限公司 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
CN118401510A (zh) * 2021-12-15 2024-07-26 日东制药株式会社 1-磺酰基吡咯衍生物的新颖盐类、其制备方法及包含其的药物组合物
KR20230102353A (ko) * 2021-12-30 2023-07-07 주식회사 대웅제약 삼중음성유방암의 예방 또는 치료용 약학적 조성물
KR102749187B1 (ko) 2022-01-24 2025-01-03 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
KR20250014615A (ko) * 2023-07-21 2025-02-03 한림제약(주) 보노프라잔 푸마르산염의 제조방법
CN117050009A (zh) * 2023-08-17 2023-11-14 台州臻挚生物科技有限公司 一种4-三氟甲基吡啶中间体核心母核及其衍生物的制备方法
KR20250095434A (ko) 2023-12-19 2025-06-26 주식회사 경보제약 보노프라잔 토실레이트 염, 이의 제조방법 및 이를 포함하는 약제학적 조성물
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
CN118108705A (zh) * 2024-01-29 2024-05-31 浙江工业大学 一种富马酸沃诺拉赞的制备方法
WO2025181220A1 (en) 2024-02-29 2025-09-04 Dipharma Francis S.R.L. Process of purifying a drug used in the treatment of acid-related disorders

Family Cites Families (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2031514T3 (es) 1986-08-29 1992-12-16 Pfizer Inc. 2-guanidino-4-ariltiazoles para el tratamiento de ulceras pepticas.
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
WO1993007751A1 (en) 1991-10-18 1993-04-29 Monsanto Company Fungicides for the control of take-all disease of plants
ZA927272B (en) 1991-10-29 1994-03-23 Du Pont Herbicidal triazolecarboxamides
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
NZ334256A (en) 1996-08-28 2000-11-24 Procter & Gamble 1-substituted sulphonyl-pyrrolidine derivatives useful as metalloprotease inhibitors
HUP0000735A3 (en) 1996-12-23 2002-03-28 Bristol Myers Squibb Pharma 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
AU2825000A (en) 1999-03-10 2000-09-28 Shionogi & Co., Ltd. Medicinal compositions with (2.2.1) and (3.1.1) bicycloskeleton antagonistic to both of pgd2/txa2 receptors
TW575561B (en) 1999-03-25 2004-02-11 Hoffmann La Roche 1-arenesulfonyl-2-aryl-pyrrolidine and piperidine derivatives
DE19913483A1 (de) 1999-03-25 2000-09-28 Goedecke Ag Verfahren zur Herstellung von Heterocyclischen Carbamaten aus Aza-Heterocyclen und Kohlendioxid
AU3783100A (en) 1999-06-14 2000-12-21 Dow Agrosciences Llc Substituted triazoles, imidazoles and pyrazoles as herbicides
AU7812900A (en) * 1999-08-26 2001-03-19 Aventis Pharmaceuticals Inc. Substituted (aminoiminomethyl or aminomethyl) dihydrobenzofurans and benozopyrans
CA2410338A1 (en) 2000-05-22 2001-11-29 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
EP1432693A2 (en) 2001-10-01 2004-06-30 Taisho Pharmaceutical Co. Ltd. Mch receptor antagonists
CA2466375A1 (en) 2001-11-08 2003-05-15 Pharmacia & Upjohn Company Azabicyclic-substituted-heteroaryl compounds for the treatment of disease
JP2005520792A (ja) 2001-11-22 2005-07-14 チバ　スペシャルティ　ケミカルズ　ホールディング　インコーポレーテッド ピロール合成
WO2003057669A1 (fr) 2001-12-28 2003-07-17 Takeda Chemical Industries, Ltd. Antagonistes du recepteur androgene
WO2003068738A1 (en) 2002-02-11 2003-08-21 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
ES2297204T3 (es) * 2002-05-17 2008-05-01 Merckle Gmbh Compuestos pirrolicos recocidos como inhibidores de la bomba de protones para el tratamiento de la ulcera.
CN100335477C (zh) 2002-06-13 2007-09-05 纳幕尔杜邦公司 吡唑甲酰胺杀虫剂
DE10228103A1 (de) 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
JP2006501217A (ja) 2002-08-12 2006-01-12 スージェン・インコーポレーテッド 新規キナーゼ阻害剤としての３−ピロリル−ピリドピラゾールおよび３−ピロリル−インダゾール
JP2004315511A (ja) 2003-03-31 2004-11-11 Taisho Pharmaceut Co Ltd Ｍｃｈ受容体アンタゴニスト
JP4716996B2 (ja) 2003-05-26 2011-07-06 武田薬品工業株式会社 スルホピロール
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
EP1769092A4 (en) 2004-06-29 2008-08-06 Europ Nickel Plc IMPROVED LIXIVIATION OF BASE METALS
EP1803709B1 (en) * 2004-09-30 2013-01-02 Takeda Pharmaceutical Company Limited Proton pump inhibitors
JP2006100626A (ja) 2004-09-30 2006-04-13 Fuji Photo Film Co Ltd 半導体発光装置
EP1655284A1 (en) 2004-10-26 2006-05-10 Aponetics AG 2-Phenylsulfopyrroles
ATE504567T1 (de) * 2005-08-30 2011-04-15 Takeda Pharmaceutical 1-heterocyclylsulfonyl, 2-aminomethyl, 5- (hetero-) aryl-substitutierte 1-h-pyrrolderivate als säuresekretionshemmer
KR101366856B1 (ko) * 2007-03-29 2014-02-21 삼성전자주식회사 다양한 포트를 통해 입력되는 영상을 디스플레이하는디스플레이 장치

Also Published As

Publication number Publication date
CY1111922T1 (el) 2015-11-04
CN101300229B (zh) 2011-10-05
PT2327692E (pt) 2012-10-11
US20110144161A1 (en) 2011-06-16
BR122017028096B8 (pt) 2021-05-25
EP2327692B1 (en) 2012-07-18
TWI358296B (en) 2012-02-21
KR20110091826A (ko) 2011-08-12
PT1919865E (pt) 2011-07-11
HK1118547A1 (en) 2009-02-13
JP5687293B2 (ja) 2015-03-18
ZA200802488B (en) 2009-06-24
US8338462B2 (en) 2012-12-25
RS51697B (sr) 2011-10-31
DE602006021195D1 (en) 2011-05-19
PE20110009A1 (es) 2011-01-31
NZ566378A (en) 2011-03-31
KR101115857B1 (ko) 2012-04-12
EP2327692B9 (en) 2014-06-04
JP4035559B1 (ja) 2008-01-23
US20070060623A1 (en) 2007-03-15
RU2415838C2 (ru) 2011-04-10
RU2008112153A (ru) 2009-10-10
MEP10009A (en) 2011-12-20
PL1919865T3 (pl) 2011-09-30
AU2006285641A1 (en) 2007-03-08
DK1919865T3 (da) 2011-05-23
IL189375A0 (en) 2008-06-05
US8299261B2 (en) 2012-10-30
WO2007026916A1 (en) 2007-03-08
US8436187B2 (en) 2013-05-07
ME00610B (me) 2011-12-20
BRPI0615111B8 (pt) 2021-05-25
CY1114415T1 (el) 2016-12-14
EP2327692A1 (en) 2011-06-01
PL2327692T3 (pl) 2012-12-31
JP2013100316A (ja) 2013-05-23
KR101408561B1 (ko) 2014-06-19
US20090143444A1 (en) 2009-06-04
CA2621182C (en) 2014-03-18
US20110301173A1 (en) 2011-12-08
US20110301174A1 (en) 2011-12-08
EP1919865B1 (en) 2011-04-06
MA29773B1 (fr) 2008-09-01
GEP20105044B (en) 2010-07-12
HRP20120792T1 (hr) 2012-10-31
US8338461B2 (en) 2012-12-25
AR055144A1 (es) 2007-08-08
SI2327692T1 (sl) 2012-11-30
HRP20110473T1 (hr) 2011-07-31
ES2391757T3 (es) 2012-11-29
SI1919865T1 (sl) 2011-07-29
CN101300229A (zh) 2008-11-05
BRPI0615111B1 (pt) 2020-02-18
JP5204426B2 (ja) 2013-06-05
JP2008056659A (ja) 2008-03-13
BR122017028096B1 (pt) 2021-04-13
RS52473B (sr) 2013-02-28
US20090275591A1 (en) 2009-11-05
US7498337B2 (en) 2009-03-03
ATE504567T1 (de) 2011-04-15
PE20070540A1 (es) 2007-06-26
US20120088797A1 (en) 2012-04-12
TW200800185A (en) 2008-01-01
HK1158627A1 (en) 2012-07-20
JO2791B1 (en) 2014-03-15
KR20080039998A (ko) 2008-05-07
US8415368B2 (en) 2013-04-09
ES2364498T3 (es) 2011-09-05
IL189375A (en) 2013-05-30
DK2327692T5 (da) 2014-06-23
NO341894B1 (no) 2018-02-12
RS52473B9 (sr) 2019-07-31
US7977488B2 (en) 2011-07-12
JP2008522952A (ja) 2008-07-03
CA2621182A1 (en) 2007-03-08
EP1919865A1 (en) 2008-05-14
CR9755A (es) 2013-06-14
BRPI0615111A2 (pt) 2011-05-03
DK2327692T3 (da) 2012-10-15
NO20081464L (no) 2008-05-23

Similar Documents

Publication Publication Date Title
UA94424C2 (en) 1-heterocyclylsulfonyl, 2-aminomethyl, 5-(hetero-)aryl substituted 1-h-pyrrole derivatives as acid secretion inhibitors
TW200633991A (en) Chemical compounds
EA200601852A1 (ru) Тетрагидрохинолиновые производные и способ их получения
MX2011008305A (es) Compuestos de piridazinona.
WO2008108380A3 (en) Pyrrole compounds
MY160394A (en) Novel phenol derivative
NO20080942L (no) Amino-5-[4-(difluormetoksy)-fenyl]-5-fenylimidazolonforbindelser som inhibitorer av beta-sekretase (BACE)
TW200612947A (en) Organic compounds
MY146532A (en) Thiazole derivative
NO20072963L (no) 5-substituerte kinolin- og isokinolinderivater, fremgangsmate for deres fremstilling og deres anvendelse som betennelseshemmere
NO20082209L (no) Homo- og heterocykliske forbindelser anvendbare som CETP-inhibitorer
WO2009057784A1 (ja) 複素環化合物
WO2008057775A3 (en) Heterocyclic amide compounds useful as kinase inhibitors
TW200640862A (en) Pyridyl acetic acid compounds
WO2009038064A1 (ja) Ｉ型１１βヒドロキシステロイド脱水素酵素阻害活性を有する複素環誘導体
WO2005095395A3 (en) Tetrahydronaphthyridine derivatives as cholesteryl ester transfer protein inhibitors
WO2008126901A1 (ja) 含窒素複素環化合物およびそれを含有する医薬組成物
GEP20125637B (en) Tricyclic compounds having corticotropin-releasing factor antagonistic activity and pharmaceutical compositions containing them
NO20082118L (no) Heterocykliske CETP-inhibitorer
EA201071012A1 (ru) Производные азетидинов, способ их получения и применение их в терапии
WO2008114812A1 (ja) Jak阻害剤
EP1867331A4 (en) TRIAZOLE DERIVATIVE AND USE THEREOF
ATE491704T1 (de) 4-ä2-(cycloalkylamino)pyrimidin-4-ylü- (phenyl)imidazolin-2-onderivate als inhibitoren der p38-map-kinase zur behandlung von entzündlichen krankheiten
ATE308541T1 (de) 2-amino-4-heteroarylethyl-thiazolinderivate und ihre verwendung als hemmstoffe der induzierbaren no-synthase
PL1692098T3 (pl) Pochodna alfa-ketomidu oraz sposób jej wytwarzania i zastosowanie