AR049168A1 - Derivados de benzimidazol - Google Patents

Derivados de benzimidazol

Info

Publication number
AR049168A1
AR049168A1 ARP050101885A ARP050101885A AR049168A1 AR 049168 A1 AR049168 A1 AR 049168A1 AR P050101885 A ARP050101885 A AR P050101885A AR P050101885 A ARP050101885 A AR P050101885A AR 049168 A1 AR049168 A1 AR 049168A1
Authority
AR
Argentina
Prior art keywords
alkoxy
alkyl
hydroxy
hydrogen
amino
Prior art date
Application number
ARP050101885A
Other languages
English (en)
Inventor
Peter Jan Zimmermann
Buhr Wilm Dr
Chiesa M Vittoria Dr
Andreas Palmer
Brehm Christof Dr
Simon Wolfgang-Alexander Dr
Postius Stefan Dr
Dr Kromer Wolfgang Prof
Original Assignee
Altana Pharma Ag
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 Altana Pharma Ag filed Critical Altana Pharma Ag
Publication of AR049168A1 publication Critical patent/AR049168A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/08Radicals containing only hydrogen and carbon atoms
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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

Abstract

Reivindicacion 1: Un nuevo compuesto de 6-bencimidazol substituido, caracterizado por la formula (1), donde: R1 es hidrogeno, alquilo C1-4, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, alcoxi C1-4, alcoxi C1-4-alquilo C1-4, alcoxi C1-4- carbonilo, alquenilo C2-4, alquinilo C2-4, fluoro-alquilo C1-4, hidroxi-alquilo C1-4, mono- o di-alquil C1-4-amino o alquil C1-4-carboniloxi-alquilo C1-4; R2 es hidrogeno, alquilo C1-4, arilo, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-4, alcoxi C1-4-carbonilo, mono- o di-alquil C1-4-amino-alquil C1-4-carbonilo, hidroxi-alquilo C1-4, fluoro-alquilo C2-4, aril C1-4-alcoxi C1-4-alquilo C1-4, hidroxi o alcoxi C1-4; R3 es hidrogeno, halogeno, fluoro-alquilo C1-4, carboxilo, -CO-alcoxi C1-4, hidroxi-alquilo C1-4, alcoxi C1-4-alquilo C1-4, alcoxi C1-4-alcoxi C1-4-alquilo C1-4, fluoro-alcoxi C1-4-alquilo C1-4, ciano, el grupo -CO-NR31R32, el grupo SO2-NR31R32 o el grupo Het; donde R31 es hidrogeno, hidroxilo, alquilo C1-7, hidroxi-alquilo C1-4, alcoxi C1-4-alquilo C1-4 o cicloalquilo C3-7, amino; y R32 es hidrogeno, alquilo C1-7, hidroxi-alquilo C1-4 o alcoxi C1-4-alquilo C1-4; o donde R31 y R32 tomados conjuntamente, incluyendo el átomo de nitrogeno al cual están ligados, son un grupo pirrolidino, piperidino, piperazino, N-alquil C1-4-piperazino, morfolino, aziridino o acetidino; y Het es un residuo heterocíclico, sustituido por R33, R34 y R35, seleccionado del grupo formado por oxadiazol, dihidrooxazol, dihidroimidazol, oxazol, imidazol, isoxazol, dihidroisoxazol, pirazol y tetrazol; donde R33 es hidrogeno, alquilo C1-4, hidroxi-alquilo C1-4, alcoxi C1-4, alqueniloxi C2-4, alquil C1-4-carbonilo, carboxi, alcoxi C1-4-carbonilo, carboxi-alquilo C1-4, alcoxi C1-4- carbonil-alquilo C1-4, halogeno, hidroxi, arilo, aril-alquilo C1-4, aril-oxi, aril-alcoxi C1-4, trifluorometilo, nitro, amino, mono- o di-alquil C1-4-amino, alquil C1-4-carbonilamino, alcoxi C1-4-carbonilamino, alcoxi C1-4-alcoxi C1-4-carbonilamino o sulfonilo; R34 es hidrogeno, alquilo C1-4, alcoxi C1-4, alcoxi C1-4-carbonilo, halogeno, trifluorometilo o hidroxi; R35 es hidrogeno, alquilo C1-4, alcoxi C1-4, alcoxi C1-4-carbonilo, halogeno, trifluorometilo o hidroxi; X es O (oxígeno) o NH; y Y o tiene el significado -CH2-Ar; donde Ar es un residuo aromático mono- o bicíclico, sustituido por R4, R5, R6 y R7, que es seleccionado del grupo formado por fenilo, naftilo, pirrolilo, pirazolilo, imidazolilo, 1,2,3-triazolilo, indolilo, bencimidazolilo, furilo, benzofurilo, tienilo, benzotienilo, tiazolilo, isoxazolilo, piridinilo, pirimidinilo, quinolinilo o isoquinolinilo; o Y significado el grupo de formula (2), donde Z tiene el significado -CHR8- o -CHR8-CHR9- donde en Ar y/o en el grupo de formula (2); R4 es hidrogeno, alquilo C1-4, hidroxi-alquilo C1-4, alcoxi C1-4, alqueniloxi C2-4, alquil C1-4-carbonilo, carboxi, alcoxi C1-4-carbonilo, carboxi-alquilo C1-4, alcoxi C1-4-carbonil-alquilo C1-4, halogeno, hidroxi, arilo, aril-alquilo C1-4, aril-oxi, aril-alcoxi C1-4, trifluorometilo, fluoro-alcoxi C1-4, nitro, amino, mono- o di-alquil C1-4-amino, alquil C1-4-carbonilamino, alcoxi C1-4-carbonilamino, alcoxi C1-4-alcoxi C1-4-carbonilamino o sulfonilo; R5 es hidrogeno, alquilo C1-4, alcoxi C1-4, alcoxi C1-4-carbonilo, halogeno, trifluorometilo o hidroxi; R6 es hidrogeno, alquilo C1-4 o halogeno; y R7 es hidrogeno, alquilo C1-4 o halogeno; R8 es hidrogeno, alquilo C1-7, alquenilo C2-7, hidroxilo, alcoxi C1-4, alcoxi C1-4, oxo-substituido, cicloalcoxi C3-7, cicloalquil C3-7-alcoxi C1-4, hidroxi-alcoxi C1-4, alcoxi C1-4-alcoxi C1-4, alcoxi C1-4-alcoxi C1-4-alcoxi C1-4, cicloalcoxi C3-7-alcoxi C1-4, cicloalquil C3-7-alcoxi C1-4-alcoxi C1-4, alquil C1-4- carboniloxi, halo-alcoxi C1-4, amino, mono- o di-alquil C1-4-amino, alquil C1-4-carbonilamino, alcoxi C1-4-carbonilamino, mono- o di-alquil C1-4-amino-alquil C1-4-carboniloxi, alcoxi C1-4-alcoxi C1-4-carbonilamino o alcoxi C1-4-alquil C1-4- carboniloxi; R9 es hidrogeno, alquilo C1-7, alquenilo C2-7, hidroxilo, alcoxi C1-4, alcoxi C1-4 oxo-sustituido, cicloalcoxi C3-7, cicloalquil C3-7-alcoxi C1-4, hidroxi-alcoxi C1-4, alcoxi C1-4-alcoxi C1-4, alcoxi C1-4-alcoxi C1-4-alcoxi C1-4, cicloalcoxi C3-7-alcoxi C1-4, cicloalquil C3-7-alcoxi C1-4-alcoxi C1-4, alquil C1-4-carboniloxi, halo-alcoxi C1-4, amino, mono- o di-alquil C1-4-amino, alquil C1-4-carbonilamino, alcoxi C1-4-carbonilamino, mono- o di-alquil C1-4-amino-alquil C1-4- carboniloxi, alcoxi C1-4-alcoxi C1-4-carbonilamino o alcoxi C1-4-alquil C1-4-carboniloxi; y donde arilo es fenilo o fenilo sustituido por uno, dos o tres sustituyentes iguales o diferentes del grupo formado por alquilo C1-4, alcoxi C1-4, carboxi, alcoxi C1-4-carbonilo, halogeno, trifluorometilo, nitro, trifluorometoxi, hidroxi y ciano, y sus sales.
ARP050101885A 2004-05-18 2005-05-10 Derivados de benzimidazol AR049168A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP04102191 2004-05-18

Publications (1)

Publication Number Publication Date
AR049168A1 true AR049168A1 (es) 2006-07-05

Family

ID=34929111

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050101885A AR049168A1 (es) 2004-05-18 2005-05-10 Derivados de benzimidazol

Country Status (7)

Country Link
EP (1) EP1756067A1 (es)
JP (1) JP2007538047A (es)
AR (1) AR049168A1 (es)
AU (1) AU2005243434A1 (es)
CA (1) CA2566821A1 (es)
TW (1) TW200600502A (es)
WO (1) WO2005111000A1 (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006283876A1 (en) * 2005-08-22 2007-03-01 Nycomed Gmbh Isotopically substituted benzimidazole derivatives
WO2007031860A1 (en) * 2005-09-15 2007-03-22 Pfizer Japan Inc. Indane substituted benzimidazoles and their use as acid pump inhibitors
WO2007072142A2 (en) * 2005-12-19 2007-06-28 Pfizer Japan Inc. Benzimidazole-5-carboxamide derivatives
CA2631880C (en) * 2005-12-19 2011-03-29 Pfizer Inc. Chromane substituted benzimidazoles and their use as acid pump inhibitors
KR20190057569A (ko) * 2017-11-20 2019-05-29 제일약품주식회사 7-아미노-1h-인돌-5-카르복사미드 유도체 및 이의 용도
WO2024087155A1 (zh) * 2022-10-28 2024-05-02 深圳市华先医药科技有限公司 一种合成4-羟基-n,n,2-三甲基苯并咪唑-6-甲酰胺的方法
WO2024210689A1 (ko) * 2023-04-07 2024-10-10 제이더블유중외제약 주식회사 벤즈이미다졸 유도체의 염

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8604566D0 (sv) * 1986-10-27 1986-10-27 Haessle Ab Novel compunds
IL108520A (en) * 1993-02-15 1997-09-30 Byk Gulden Lomberg Chem Fab 2, 3, 8-TRISUBSTITUTED IMIDAZO £1, 2-a| PYRIDINE DERIVATIVES, PROCESSES FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
WO1996004251A1 (fr) * 1994-08-03 1996-02-15 Fujisawa Pharmaceutical Co., Ltd. Compose heterocyclique
SE9602286D0 (sv) * 1996-06-10 1996-06-10 Astra Ab New compounds
AR043063A1 (es) * 2002-12-13 2005-07-13 Altana Pharma Ag Bencimidazoles 6-sustituidos y su uso como inhibidores de secreciones gastricas

Also Published As

Publication number Publication date
CA2566821A1 (en) 2005-11-24
JP2007538047A (ja) 2007-12-27
AU2005243434A1 (en) 2005-11-24
EP1756067A1 (en) 2007-02-28
WO2005111000A1 (en) 2005-11-24
TW200600502A (en) 2006-01-01

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