[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

YU48714B - Derivati benzofurana, benzotiofena, indola i indolizina i postupak za njihovo dobijanje - Google Patents

Derivati benzofurana, benzotiofena, indola i indolizina i postupak za njihovo dobijanje

Info

Publication number
YU48714B
YU48714B YU134891A YU134891A YU48714B YU 48714 B YU48714 B YU 48714B YU 134891 A YU134891 A YU 134891A YU 134891 A YU134891 A YU 134891A YU 48714 B YU48714 B YU 48714B
Authority
YU
Yugoslavia
Prior art keywords
alkyl
opt
substd
phenyl
rran
Prior art date
Application number
YU134891A
Other languages
English (en)
Other versions
YU134891A (sh
Inventor
Jean Gubin
Jean Lucchetti
Henri Inion
Pierre Chatelain
Gilbert G. Rosseels
Steven Kilenyi
Original Assignee
Sanofi-Aventis
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 Sanofi-Aventis filed Critical Sanofi-Aventis
Publication of YU134891A publication Critical patent/YU134891A/sh
Publication of YU48714B publication Critical patent/YU48714B/sh

Links

Classifications

    • 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
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/80Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/81Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/52Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
    • C07D333/54Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D333/56Radicals substituted by oxygen atoms
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Furan Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
  • Cosmetics (AREA)

Abstract

Derivati benzofurana, benzotiofena, indola i indolina, sledece opste formule: u kojoj: Het predstavlja jednu od grupa u kojima: T predstavlja grupu: u kojoj: R i Ra mogu biti identicni ili razliciti i svaka predstavlja: - vodonik, - C1-C4 alkil radikal, - radikal -SO2R' u kojem R' predstavlja C1-C6 alkil radikal, normalan ili racvast, trifluorometil radikal, fenil radikal koji je eventualno supstituisan sa C1-C4 alkil radikalom, benzil radikal koji je eventualno supstituisan sa C1-C4 alkil radikalom ili banzoil radikal koji je eventualno supstituisan sa C1-C4 alkil radikalom, Ra i R' mogu da grade sa atomom azota sulfonamidne grupe prsten koji sadrzi od 3 do 6 atoma ugljenika, T' predstavlja: - nitro grupu, - grupu R , takvu kao sto je definisano napred. T" predstavlja - benziloksikarbonilamino grupu, - grupu u kojoj T"1 predstavlja vodonik ili C1-C4 alkil grupu, - grupu u kojoj T"2 i T"3 mogu da budu identicni ili razliciti i predstavljaju vodonik ili C1-C4 alkil grupu ili T"2 i T"3 grade sa atomom azota za koji su vezani, prsten koji sadrzi od 4 do 6 atoma ugljenika, - grupu R , takvu kao sto je definisano napred, X predstavlja -O- ili -S-, Y predstavqa radikal ili -CH2- u kojem R5 predstavlja vodonik, C1-C4 alkil radikal ili acil radikal formule u kojoj R'4 predstavlja C1-C4 alkil radikal, R1 predstavlja radikal C1-C6 alkil, fenil koji je eventualno supstituisan sa radikalom C1-C4 alkil ili halogeno fenil; R2 predstavlja: - vodonik, - C1-C6 alkil linearan ili racvast; R3 predstavlja: - C1-C6 alkil linearan ili racvast; - radikal formule: -Alk-R6 u kojoj Alk predstavlja prostu vezu ili C1-C5 alkilen radikal normalan ili racvast i R6 predstavlja radikal takav kao sto je piridil, fenil, fenoksi, 3,4-metilendioksi fenil ili grupu fenil ili fenoksi koja je supstituisana sa jednim ili sa vise supstituenata, identicnih ili razlicitih koji se biraju iz grupe koja obuhvata halogene, grupu C1-C4 alkil ili C1-C4 alkoksi, R2 i R3 kada se uzmu zajedno, predstavljaju radikal C3-C6 alkilen ili C3-C6 alkenilen koji je eventualno supstituisan sa fenil radikalom ili je eventualno prekinut sa -O-, -NH-, -N= ili =N-R7, gde R7 predstavlja radikal C1-C4 alkil ili fenil; R4 predstavlja: - vodonik, - C1-C4 alkil radikal, - radikal -SO2R1' u kojem R'1 predstavlja C1-C4 alkil radikal, fenil radikal koji je eventualno supstituisan sa C1-C4 alkil radikalom, benzil radikal koji je eventualno supstitusan sa C1-C4 alkil radikalom, - radikal: u kojem R'4 i R"4, identicni ili razliciti predstavqaju C1-C4 alkil radikal i m predstavlja ceo broj od 1 do 3; A predstavlja -O-, -S- ili W, W' i Z su takvi da: - kada su identicni W i W' predstavljaju CH- ili N, Z predstavlja -O-; - kada W predstavlja i W, predstavlja , Z predstavlja -CH=C-R'8 gde R8 i R'8 su identicni ili razliciti i predstavljaju atom halogena ili radikal C1-C4 alkil ili C1-C4 alkoksi, n predstavlja ceo broj od 1 do 5, u slucaju kada R4 predstavlja radikal -SO2R'1, T', grupu nitro ili cikliziranu grupu , kao i njiho
YU134891A 1990-08-06 1991-08-05 Derivati benzofurana, benzotiofena, indola i indolizina i postupak za njihovo dobijanje YU48714B (sh)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9010036A FR2665444B1 (fr) 1990-08-06 1990-08-06 Derives d'amino-benzofuranne, benzothiophene ou indole, leur procede de preparation ainsi que les compositions les contenant.

Publications (2)

Publication Number Publication Date
YU134891A YU134891A (sh) 1994-01-20
YU48714B true YU48714B (sh) 1999-07-28

Family

ID=9399463

Family Applications (1)

Application Number Title Priority Date Filing Date
YU134891A YU48714B (sh) 1990-08-06 1991-08-05 Derivati benzofurana, benzotiofena, indola i indolizina i postupak za njihovo dobijanje

Country Status (32)

Country Link
US (1) US5223510A (sh)
EP (1) EP0471609B1 (sh)
JP (1) JP2795759B2 (sh)
KR (1) KR100190673B1 (sh)
AT (1) ATE145645T1 (sh)
BR (1) BR9103354A (sh)
CA (1) CA2047773C (sh)
CZ (1) CZ288527B6 (sh)
DE (1) DE69123304T2 (sh)
DK (1) DK0471609T3 (sh)
ES (1) ES2096639T3 (sh)
FI (1) FI114914B (sh)
FR (1) FR2665444B1 (sh)
GR (1) GR3022593T3 (sh)
HK (1) HK1000108A1 (sh)
HU (2) HU218271B (sh)
IE (1) IE912595A1 (sh)
IL (1) IL98991A (sh)
MA (1) MA22249A1 (sh)
MY (1) MY107655A (sh)
NO (1) NO179042C (sh)
NZ (1) NZ239232A (sh)
OA (1) OA09513A (sh)
PL (1) PL168044B1 (sh)
PT (1) PT98576B (sh)
RU (1) RU2095357C1 (sh)
SG (1) SG49205A1 (sh)
SK (1) SK283527B6 (sh)
TN (1) TNSN91070A1 (sh)
TW (1) TW199095B (sh)
YU (1) YU48714B (sh)
ZA (1) ZA915934B (sh)

Families Citing this family (182)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU668691B2 (en) * 1991-08-09 1996-05-16 Nycomed Innovation Ab Use of persistent free-radicals in magnetic resonance imaging
US6756388B1 (en) * 1993-10-12 2004-06-29 Pfizer Inc. Benzothiophenes and related compounds as estrogen agonists
DE4420925A1 (de) * 1994-06-16 1995-12-21 Bayer Ag Verfahren zur Herstellung von Benzthiophenderivaten
US5596106A (en) * 1994-07-15 1997-01-21 Eli Lilly And Company Cannabinoid receptor antagonists
GB9416219D0 (en) * 1994-08-11 1994-10-05 Karobio Ab Receptor ligands
US5856340A (en) * 1995-02-28 1999-01-05 Eli Lilly And Company Method of treating estrogen dependent cancers
US5998441A (en) * 1995-02-28 1999-12-07 Eli Lilly And Company Benzothiophene compounds, intermediates, compositions, and methods
US5977093A (en) * 1995-02-28 1999-11-02 Eli Lilly And Company Benzothiophene compounds, intermediates, compositions, and methods
US5510357A (en) * 1995-02-28 1996-04-23 Eli Lilly And Company Benzothiophene compounds as anti-estrogenic agents
US5919800A (en) * 1995-02-28 1999-07-06 Eli Lilly And Company Benzothiophene compounds, intermediates, compositions, and methods
US5856339A (en) * 1995-02-28 1999-01-05 Eli Lilly And Company Benzothiophene compounds, intermediates, compositions, and methods
US5998401A (en) 1995-02-28 1999-12-07 Eli Lilly And Company Naphthyl compounds, intermediates, compositions, and methods
US6391892B1 (en) * 1995-03-10 2002-05-21 Eli Lilly And Company Naphthyl pharmaceutical compounds
US6417199B1 (en) * 1995-03-10 2002-07-09 Eli Lilly And Company 3-benzyl-benzothiophenes
US6395755B1 (en) * 1995-03-10 2002-05-28 Eli Lilly And Company Benzothiophene pharmaceutical compounds
CA2214850A1 (en) * 1995-03-13 1996-09-19 Eli Lilly And Company Novel benzothiophene compounds and methods
FR2735365B1 (fr) * 1995-06-14 1997-09-05 Sanofi Sa Utilisation d'un antagoniste de l'angiotensine ii et d'un derive du benzofurane pour la preparation d'un medicament utile dans le traitement des affections cardiovasculaires
US6432982B1 (en) * 1996-02-21 2002-08-13 Eli Lilly And Company Benzothiophenes, and formulations and methods using same
FR2746013B1 (fr) * 1996-03-18 1998-05-29 Sanofi Sa Utilisation de composes antiarythmiques dans la prevention de la mortalite post infarctus
US6008377A (en) * 1996-03-19 1999-12-28 Eli Lilly And Company Synthesis of 3-[4-(2-aminoethoxy)-benzoyl]-2-aryl-6-hydroxy-benzo[B]thiophenes
US5958969A (en) * 1996-10-10 1999-09-28 Eli Lilly And Company Benzo b!thiophene compounds, intermediates, formulations, and methods
ZA982877B (en) * 1997-04-09 1999-10-04 Lilly Co Eli Treatment of central nervous system disorders with selective estrogen receptor modulators.
WO1998048792A1 (en) * 1997-04-30 1998-11-05 Eli Lilly And Company A REGIOSELECTIVE ALKYLATION PROCESS FOR PREPARING SUBSTITUTED BENZO[b]THIOPHENES
CA2231013A1 (en) * 1997-04-30 1998-10-30 Eli Lilly And Company Process for preparing benzoic acid derivative intermediates and benzothiophene pharmaceuticals
AU7261598A (en) * 1997-04-30 1998-11-24 Eli Lilly And Company Intermediates and a process for preparing benzo{b}thiophenes
JP2001523253A (ja) * 1997-04-30 2001-11-20 イーライ・リリー・アンド・カンパニー ベンゾ[b]チオフェン類の製造のための中間体および方法
CA2236254A1 (en) * 1997-04-30 1998-10-30 David Warren Hoard Process for preparing benzo¬b|thiophenes
CA2287943A1 (en) * 1997-04-30 1998-11-05 Tony Yantao Zhang Processes for preparing benzothiophenes
FR2764800B1 (fr) * 1997-06-23 1999-09-10 Sanofi Sa Composition pharmaceutique solide contenant des derives de benzofuranne
US20010009965A1 (en) * 1998-05-04 2001-07-26 Alexandros Makriyannis Novel analgesic and immunomodulatory cannabinoids
US6166069A (en) * 1998-05-12 2000-12-26 American Home Products Corporation Phenyl oxo-acetic acids useful in the treatment of insulin resistance and hyperglycemia
US7589220B2 (en) * 1998-06-09 2009-09-15 University Of Connecticut Inhibitors of the anandamide transporter
US7897598B2 (en) * 1998-06-09 2011-03-01 Alexandros Makriyannis Inhibitors of the anandamide transporter
US6391899B1 (en) * 1998-07-17 2002-05-21 North Shore—Long Island Jewish Research Institute Compounds and compositions for treating tissue ischemia
US7161016B1 (en) 1998-11-24 2007-01-09 University Of Connecticut Cannabimimetic lipid amides as useful medications
US7276613B1 (en) 1998-11-24 2007-10-02 University Of Connecticut Retro-anandamides, high affinity and stability cannabinoid receptor ligands
US8084467B2 (en) * 1999-10-18 2011-12-27 University Of Connecticut Pyrazole derivatives as cannabinoid receptor antagonists
US7741365B2 (en) * 1999-10-18 2010-06-22 University Of Connecticut Peripheral cannabinoid receptor (CB2) selective ligands
MXPA02005103A (es) 1999-10-18 2003-09-25 Alexipharma Inc Ligandos selectivos del receptor de canabinoide (cb2) perifericos.
US7119108B1 (en) 1999-10-18 2006-10-10 University Of Connecticut Pyrazole derivatives as cannabinoid receptor antagonists
US7393842B2 (en) * 2001-08-31 2008-07-01 University Of Connecticut Pyrazole analogs acting on cannabinoid receptors
US6900236B1 (en) * 1999-10-18 2005-05-31 University Of Connecticut Cannabimimetic indole derivatives
CA2387138A1 (en) * 1999-10-18 2001-04-26 University Of Connecticut Cannabimimetic indole derivatives
US6943266B1 (en) 1999-10-18 2005-09-13 University Of Connecticut Bicyclic cannabinoid agonists for the cannabinoid receptor
US6555697B1 (en) 1999-10-21 2003-04-29 Rhodia Chimie Method of preparing a benzofuran or benzothiophene compound
FR2800064B1 (fr) * 1999-10-21 2002-10-11 Rhodia Chimie Sa Procede de preparation d'un compose de type benzofurane ou benzothiophene
FR2809397B1 (fr) * 2000-05-24 2002-07-19 Rhodia Chimie Sa Procede de preparation d'un compose de type benzofuranne ou benzothiophene
FR2800067B1 (fr) * 1999-10-21 2004-12-17 Rhodia Chimie Sa Intermediaires de fabrication d'un derive de type benzofurane ou benzothiophene nitre en position 5 et leurs utilisations
FR2803846B1 (fr) * 2000-01-17 2002-04-05 Clariant France Sa 3-(1-hydroxy-pentylidene)-5-nitro-3h-benzofuran-2-one, son procede de preparation et son utilisation
FR2813307B1 (fr) * 2000-08-23 2002-11-08 Sanofi Synthelabo Aminoalkenylbenzoyl-benzofurannes ou benzothiophenes, leur procede de preparation et les compositions les contenant
FR2813306B1 (fr) * 2000-08-23 2005-10-21 Sanofi Synthelabo Aminoalkybenzoyl-benzofurannes ou benzothiophenes, leur procede de preparation et les compositions les contenant
FR2813308B1 (fr) * 2000-08-23 2005-07-01 Sanofi Synthelabo Aminoalkoxybenzoyl-benzofurannes ou benzothiophenes, leur procede de preparation ainsi que les compositions les contenant
EP1335722B1 (en) * 2000-11-24 2006-08-30 Smithkline Beecham Plc Indolyl-sulfonyl- compounds useful in the treatment of cns disorders
FR2817865B1 (fr) * 2000-12-11 2005-02-18 Sanofi Synthelabo Derive aminoalkoxybenzoyle sous forme de sel, son procede de preparation et son utilisation comme intermediaire de synthese
FR2817864B1 (fr) 2000-12-11 2003-02-21 Sanofi Synthelabo Derive de methanesulfonamido-benzofurane, son procede de preparation et son utilisation comme intermediaire de synthese
US7329651B2 (en) * 2001-01-26 2008-02-12 University Of Connecticut Cannabimimetic ligands
EP1363632B1 (en) 2001-01-29 2010-08-25 The University of Connecticut Receptor selective cannabimimetic aminoalkylindoles
DE10129119B4 (de) * 2001-06-16 2007-10-04 Schwarz Pharma Ag Kristalline Salze von Benzoylbenzofuran-Derivaten, insbesondere von[2-(4-{1-[2-((S)-sec.-Butoxycarbonylmethyl)-benzofuran-3-carbonyl]-methanoyl}-2,6-diiod-phenoxy)-ethyl]-diethylamino und [2-(4-{1-[(3-Methyl-2-(S)-Butoxycarbonylmethyl)-benzofuran-3-carbonyl]- methanoyl}-2,6-diiodphenoxy)-ethyl]-diethylamino, deren Verwendung und Herstellung sowie diese Salze enthaltende Arzneimittel
US7208495B2 (en) 2001-07-05 2007-04-24 Takeda Pharmaceutical Company Limited Benzo-fused 5-membered hetrocycle compounds, process for preparation of the same, and use thereof
CA2452881C (en) * 2001-07-13 2012-03-06 University Of Connecticut Novel bicyclic and tricyclic cannabinoids
WO2003035005A2 (en) * 2001-10-26 2003-05-01 University Of Connecticut Heteroindanes: a new class of potent cannabimimetic ligands
IL146389A0 (en) * 2001-11-08 2002-07-25 Isp Finetech Ltd Process for the preparation of dronedarone
FR2833263A1 (fr) * 2001-12-06 2003-06-13 Rhodia Chimie Sa Procede de preparation d'un compose de type aminobenzofuranne ou aminobenzothiophene
FR2833262A1 (fr) * 2001-12-06 2003-06-13 Rhodia Chimie Sa Procede de monosulfonylation d'un compose de type aminobenzofuranne ou aminobenzothiophene
DE10237819A1 (de) * 2002-08-19 2004-03-04 Bayer Ag 5-Nitrobenzofurane
CA2496097A1 (en) 2002-08-23 2004-03-04 University Of Connecticut Keto cannabinoids with therapeutic indications
US20070010573A1 (en) * 2003-06-23 2007-01-11 Xianqi Kong Methods and compositions for treating amyloid-related diseases
EP1658264A2 (en) * 2003-06-23 2006-05-24 Neurochem (International) Limited Methods and compositions for treating amyloid-related diseases
ES2222827B1 (es) * 2003-07-30 2006-03-01 Laboratorios Del Dr. Esteve, S.A. Derivados de 5-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos.
FR2859997B1 (fr) * 2003-09-18 2006-02-03 Sanofi Synthelabo Nouveaux derives d'indolizine 1,2,3,6,7,8 substituee, inhibiteurs des fgfs, leur procede de preparation et les compositions pharmaceutiques les contenant.
FR2864536B1 (fr) 2003-12-24 2006-03-17 Clariant France Sa Procede de preparation de n-alkyl-2 (hydroxy-4-benzoyl)-3 benzofurannes et intermediaires pour sa mise en oeuvre
FR2893616B1 (fr) * 2005-11-23 2008-01-04 Sanofi Aventis Sa Nouveaux derives d'indolizine, leur procede de preparation et les compositions therapeutiques les comprenant
GB0611210D0 (en) * 2006-06-07 2006-07-19 Cambrex Karlskoga Ab Process
FR2914644B1 (fr) * 2007-04-06 2009-06-05 Finorga Soc Par Actions Simpli Procede de preparation de 2-(n-butyl)-3-(4-hydroxybenzoyl) -5-nitrobenzofurane
US20090076137A1 (en) * 2007-09-19 2009-03-19 Protia, Llc Deuterium-enriched dronedarone
GB0719180D0 (en) * 2007-10-02 2007-11-14 Cambrex Karlskoga Ab New process
FR2930149B1 (fr) * 2008-04-17 2011-02-18 Sanofi Aventis Association de dronedarone avec au moins un diuretique, son application en therapeutique
US8410167B2 (en) * 2008-04-17 2013-04-02 Sanofi Use of dronedarone for the preparation of a medicament for use in the prevention of cardiovascular hospitalization or of mortality
EP2116239A1 (en) 2008-04-29 2009-11-11 Sanofi-Aventis Method for managing the risks associated with an increase in serum creatinine during dronedarone treatment
EP2153830A1 (en) 2008-08-07 2010-02-17 Sanofi-Aventis Use of dronedarone for the preparation of a medicament intended for the prevention of stroke or transient ischemic attack
CN102171200B (zh) * 2008-10-02 2015-09-30 坎布雷卡尔斯库加公司 用于制备二酮类和药物的方法
JP2012505163A (ja) * 2008-10-10 2012-03-01 ロンザ リミテッド 2−アルキル−3−アロイル−5−ニトロ−ベンゾフランの調製方法
EP2246341A1 (en) 2009-01-23 2010-11-03 Lonza Ltd. Process for preparing 2-Alkyl-3-aroyl-5-nitro-benzofurans
EP2417099B1 (en) * 2009-04-08 2015-12-23 Cambrex Karlskoga AB New process for preparing hydroxylamines and medicaments
TW201111354A (en) 2009-05-27 2011-04-01 Sanofi Aventis Process for the production of Dronedarone intermediates
UY32656A (es) 2009-05-27 2010-12-31 Sanofi Aventis Procedimiento para producir benzofuranos
CN101993427B (zh) * 2009-08-26 2012-10-10 成都伊诺达博医药科技有限公司 一种制备决奈达隆的方法
HUP0900759A2 (en) * 2009-12-08 2011-11-28 Sanofi Aventis Novel process for producing dronedarone
TWI508726B (zh) 2009-12-21 2015-11-21 Gilead Sciences Inc 治療心房纖維性顫動之方法
HUP1000010A2 (en) 2010-01-08 2011-11-28 Sanofi Sa Process for producing dronedarone
EP2354132A2 (en) 2010-02-05 2011-08-10 Sanofi Crystallized form of dronedarone base
MX2012009299A (es) * 2010-02-10 2012-09-12 Mapi Pharma Ltd Preparacion de benzofuranos y su uso como intermedios sinteticos.
FR2957079B1 (fr) * 2010-03-02 2012-07-27 Sanofi Aventis Procede de synthese de derives de cetobenzofurane
EP2371824A1 (en) 2010-03-08 2011-10-05 Ratiopharm GmbH Crystalline dronedarone salts
EP2371808A1 (en) 2010-03-08 2011-10-05 Ratiopharm GmbH Process for preparing dronedarone
EP2364703A1 (en) 2010-03-12 2011-09-14 Sanofi Use of dronedarone or a pharmaceutically acceptable salt thereof, for the preparation of a medicament for administration shortly after amiodarone discontinuation
FR2958289B1 (fr) * 2010-03-30 2012-06-15 Sanofi Aventis Procede de preparation de derives de 3-ceto-benzofurane
FR2958290B1 (fr) 2010-03-30 2012-10-19 Sanofi Aventis Procede de preparation de derives de sulfonamido-benzofurane
FR2958291B1 (fr) * 2010-04-01 2013-07-05 Sanofi Aventis Procede de preparation de derives d'amino-benzofurane
WO2011135581A2 (en) 2010-04-28 2011-11-03 Cadila Healthcare Limited Pharmaceutical compositions of dronedarone
WO2011135582A2 (en) 2010-04-28 2011-11-03 Cadila Healthcare Limited Pharmaceutical compositions of dronedarone
EP2386300A1 (en) 2010-05-11 2011-11-16 Sanofi Use of dronedarone for the preparation of a medicament for use in the prevention of cardiovascular hospitalization or of mortality in patients having a first recurrence of atrial fibrillation or atrial flutter
EP2387996A1 (en) 2010-05-17 2011-11-23 Sanofi Use of dronedarone for the preparation of a medicament for the prevention of cardiovascular events in patients with permanent atrial fibrillation
EP2387997A1 (en) 2010-05-18 2011-11-23 Sanofi Use of dronedarone for the preparation of a medicament for the prevention of cardiovascular events in patients who developed permanent atrial fibrillation throughout the period the dronedarone is administered
AR081392A1 (es) 2010-05-13 2012-08-29 Sanofi Aventis Uso de dronedarona para la preparacion de un medicamento para la prevencion de hospitalizaciones cardiovasculares o muerte o sucesos cardiovasculares en pacientes con fibrilacion auricular permanente
CN102276561A (zh) * 2010-06-09 2011-12-14 江苏恒瑞医药股份有限公司 决奈达隆及其盐的制备方法
WO2011158178A1 (en) 2010-06-14 2011-12-22 Sanofi Use of dronedarone for the preparation of a medicament for use in the treatment of patients
HUP1000330A2 (en) 2010-06-18 2011-12-28 Sanofi Sa Process for the preparation of dronedarone and the novel intermediates
US8602215B2 (en) 2010-06-30 2013-12-10 Sanofi Methods for reducing the risk of an adverse dronedarone/beta-blockers interaction in a patient suffering from atrial fibrillation
WO2012004658A2 (en) 2010-07-09 2012-01-12 Frichem Private Limited Process for preparation of n-[2-butyl-3-[4-[3-(dibutylamino)propoxy]benzoyl]-5-benzofuranyl]methanesulfonamide, acid addition salts and product thereof
WO2012007959A1 (en) * 2010-07-16 2012-01-19 Glenmark Generics Limited Process for preparing dronedarone
EP2431033A1 (en) 2010-08-10 2012-03-21 Sanofi Dronedarone for preventing cardiovascular hospitalization or mortality in patients with lone atrial fibrillation
FR2962731B1 (fr) * 2010-07-19 2012-08-17 Sanofi Aventis Procede de preparation de derives d'amino-benzoyl-benzofurane
FR2963006B1 (fr) 2010-07-21 2013-03-15 Sanofi Aventis Procede de preparation de derives de nitro-benzofurane
HUP1000386A2 (en) * 2010-07-22 2012-05-29 Sanofi Sa Novel process for producing dronedarone
WO2012013750A1 (en) 2010-07-29 2012-02-02 Sanofi Use of dronedarone for the preparation of a medicament for the hospitalization burden in patient with atrial fibrillation
WO2012020377A1 (en) 2010-08-11 2012-02-16 Sanofi Use of dronedarone for the preparation of a medicament for rhythm- and rate-controlling in patients with atrial fibrillation
WO2012023024A2 (en) 2010-08-17 2012-02-23 Lupin Limited Controlled release formulations of dronedarone
WO2012032545A1 (en) 2010-09-08 2012-03-15 Cadila Healthcare Limited Processes for preparing dronedarone and its intermediates
US20120108828A1 (en) * 2010-09-09 2012-05-03 USV Limited, B.S.D. Marg Synthesis of dronedarone and salts thereof
CN101948455B (zh) * 2010-10-18 2012-11-14 山东邹平大展新材料有限公司 一种2-正丁基-3-(4-羟基苯甲酰基)-5-硝基苯并呋喃的制备方法
EP2447256A1 (en) 2010-10-21 2012-05-02 Laboratorios Lesvi, S.L. Process for obtaining dronedarone
CN102725279A (zh) * 2010-11-08 2012-10-10 山东邹平大展新材料有限公司 一种盐酸决奈达隆的制备方法
FR2967067A1 (fr) 2010-11-10 2012-05-11 Sanofi Aventis Composition pharmaceutique et forme galenique a base de dronedarone et son procede de preparation
EP2452938A1 (en) 2010-11-12 2012-05-16 LEK Pharmaceuticals d.d. Process for the preparation of 3-aroyl-5-aminobenzofuran derivatives
FR2967412B1 (fr) * 2010-11-17 2012-12-14 Sanofi Aventis Nouveaux derives d'indolizine, leur preparation et leur application en therapeutique
EP2469281A1 (en) 2010-12-24 2012-06-27 Sanofi Method for managing the risk of liver injury in patients receiving treatment with dronedarone
EP2469280A1 (en) 2010-12-24 2012-06-27 Sanofi Method for managing the risk of liver injury in patients receiving treatment with dronedarone
EP2468175A1 (en) 2010-12-24 2012-06-27 Sanofi Method for managing the risk of liver injury in patients receiving treatment with dronedarone
JP2013544870A (ja) 2010-12-10 2013-12-19 サノフイ 肝障害のリスク管理に使用する薬剤の調製のためのドロネダロンの使用
EP2476417A1 (en) 2011-01-14 2012-07-18 Sanofi Method for managing the risk of liver injury in patients receiving treatment with dronedarone
CN102180848A (zh) * 2010-12-31 2011-09-14 江苏万全特创医药生物技术有限公司 一种新型抗心律失常药决奈达隆的制备方法
CN102180847A (zh) * 2010-12-31 2011-09-14 江苏万全特创医药生物技术有限公司 一种决奈达隆新关键中间体的制备方法
CN102070578B (zh) * 2011-01-19 2015-10-14 上海医药工业研究院 2-正丁基-3-(4-(3-二正丁基氨基丙氧基)苯甲酰基)-5-烷酰基氨基苯并呋喃的制备方法
CN102070580B (zh) * 2011-01-19 2015-05-20 上海医药工业研究院 2-正丁基-3-(4-(3-二正丁基氨基丙氧基)苯甲酰基)-5-取代氨基苯并呋喃的制备
CN102070581B (zh) * 2011-01-19 2015-11-25 上海医药工业研究院 2-正丁基-3-(4-(3-二正丁基氨基丙氧基)苯甲酰基)-5-氨基苯并呋喃的制备
CN102070577B (zh) * 2011-01-19 2016-03-09 上海医药工业研究院 2-正丁基-3-(4-取代丙氧基苯甲酰基)-5-取代氨基苯并呋喃及其应用
CN102108070B (zh) * 2011-01-26 2013-05-22 上海优贝德生物医药有限公司 5-氨基苯并呋喃-2-甲酸酯及其中间体的制备方法
CN102153531B (zh) * 2011-01-31 2013-05-22 金春华 一种用于制备决奈达隆的中间体及其制备方法
CN102653530A (zh) * 2011-03-04 2012-09-05 浙江省医学科学院 一种苯并呋喃衍生物的制备方法及其应用
WO2012120544A2 (en) 2011-03-10 2012-09-13 Sun Pharmaceutical Industries Ltd. PROCESS FOR N-[2-n-BUTYL-3-[4-[3-(DI-n-BUTYLAMINO) PROPOXY]ENZOYL]BENZOFURAN-5-YL]METHANESULFONAMIDE HYDROCHLORIDE
CN102690249B (zh) * 2011-03-22 2014-09-17 江苏康缘药业股份有限公司 一种决奈达隆的制备方法
FR2973027A1 (fr) * 2011-03-24 2012-09-28 Sanofi Aventis Procede de synthese de derives de cetobenzofurane
HUP1100167A2 (en) * 2011-03-29 2012-11-28 Sanofi Sa Process for preparation of dronedarone by mesylation
HUP1100165A2 (en) * 2011-03-29 2012-12-28 Sanofi Sa Process for preparation of dronedarone by n-butylation
HUP1100166A2 (en) 2011-03-29 2012-12-28 Sanofi Sa Reductive amination process for preparation of dronedarone using amine intermediary compound
WO2012153225A1 (en) * 2011-05-09 2012-11-15 Alembic Pharmaceuticals Limited Improved processes for obtaining high purity of dronedarone hydrochloride
CN102321057A (zh) * 2011-06-02 2012-01-18 北京阳光诺和药物研究有限公司 N-取代的甲磺酰基胺基-苯并呋喃衍生物、其制备方法及用途
WO2012171135A1 (zh) * 2011-06-13 2012-12-20 山东邹平大展新材料有限公司 一种苯并呋喃化合物、其制备方法及用途
EP2543362A1 (en) 2011-07-07 2013-01-09 Sanofi Sustained release pharmaceutical oral solid dosage form of dronedarone or one of its pharmaceutically acceptable salts
FR2977495B1 (fr) 2011-07-07 2014-03-07 Sanofi Sa Composition pharmaceutique et forme galenique solide a haute teneur en dronedarone et son procede de preparation
US20130116586A1 (en) 2011-07-07 2013-05-09 Sanofi Use of dronedarone or a pharmaceutically acceptable salt thereof for the preparation of a drug for the prevention of atrial fibrillation
EP2543361A1 (en) 2011-07-07 2013-01-09 Sanofi Sustained release pharmaceutical oral solid dosage forms of dronedarone or one of its pharmaceutically acceptable salts
EP2543363A1 (en) 2011-07-07 2013-01-09 Sanofi Sustained release pharmaceutical oral solid dosage forms of dronedarone or one of its pharmaceutically acceptable salts
WO2013014478A1 (en) 2011-07-26 2013-01-31 Sanofi Reductive amination process for preparation of dronedarone using carboxyl intermediary compound
WO2013014480A1 (en) 2011-07-26 2013-01-31 Sanofi Process for preparation of dronedarone using amide intermediary compound
WO2013014479A1 (en) 2011-07-26 2013-01-31 Sanofi Reductive animation process for preparation of dronedarone using aldehyde intermediary compound
WO2013024411A1 (en) 2011-08-12 2013-02-21 Lupin Limited Co-milled formulation of dronedarone
ITMI20111672A1 (it) * 2011-09-16 2013-03-17 Olon Spa Metodo efficiente per la preparazione di dronedarone cloridrato
CN102382087A (zh) * 2011-10-20 2012-03-21 南京工业大学 一种盐酸决奈达隆的制备方法
FR2983198B1 (fr) 2011-11-29 2013-11-15 Sanofi Sa Procede de preparation de derives de 5-amino-benzoyl-benzofurane
EP2617718A1 (en) 2012-01-20 2013-07-24 Sanofi Process for preparation of dronedarone by the use of dibutylaminopropanol reagent
US9221778B2 (en) 2012-02-13 2015-12-29 Sanofi Process for preparation of dronedarone by removal of hydroxyl group
US9249119B2 (en) 2012-02-14 2016-02-02 Sanofi Process for the preparation of dronedarone by oxidation of a sulphenyl group
EP2817001A1 (en) 2012-02-20 2014-12-31 Lupin Limited Bilayer tablet of dronedarone
US9382223B2 (en) * 2012-02-22 2016-07-05 Sanofi Process for preparation of dronedarone by oxidation of a hydroxyl group
PE20150022A1 (es) 2012-05-22 2015-02-09 Sanofi Sa Dronedarona para uso en la leishmaniosis, formulaciones y asociaciones para uso en la leishmaniosis
CN102718735B (zh) * 2012-05-28 2014-04-23 沈阳药科大学 2-乙基-3-(4-羟基)苯甲酰基苯并呋喃类化合物、组合物及其制备方法
US9238636B2 (en) 2012-05-31 2016-01-19 Sanofi Process for preparation of dronedarone by Grignard reaction
CN102731452A (zh) * 2012-07-25 2012-10-17 中国药科大学 一种维拉唑酮中间体的制备方法
WO2014203058A1 (en) 2013-06-17 2014-12-24 Aurobindo Pharma Limited An improved process for preparing benzofuran compound
TW201536763A (zh) * 2013-08-27 2015-10-01 Gilead Sciences Inc 製備決奈達隆或其鹽類之製程
CN105315245B (zh) * 2014-06-16 2018-10-12 华润赛科药业有限责任公司 苯并呋喃类衍生物、其制备方法和应用
WO2016120299A1 (en) 2015-01-28 2016-08-04 Sanovel Ilac Sanayi Ve Ticaret A.S. Orally disintegrating formulations of dronedarone
TR201501970A2 (en) 2015-02-19 2016-09-21 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Pharmaceutical combinations of dronedarone.
TR201502223A2 (tr) 2015-02-25 2016-09-21 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dronedaron ve dabigatranın farmasötik kombinasyonları.
TR201503136A2 (tr) 2015-03-16 2016-09-21 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dronedaron ve esansiyel yağ asitlerinin farmasötik kompozisyonları.
CN104844498B (zh) * 2015-04-07 2017-10-20 陕西师范大学 一种3‑取代吲哚甲胺衍生物的制备方法
US10975051B2 (en) 2015-08-12 2021-04-13 Memorial Sloan Kettering Cancer Center Phenylsulfonamido-benzofuran derivatives and uses thereof in the treatment of proliferative diseases
CN105753822B (zh) * 2016-02-24 2018-04-03 华润赛科药业有限责任公司 一种苯并呋喃类衍生物、其制备方法和应用
CN106432159B (zh) * 2016-07-14 2019-07-12 华润赛科药业有限责任公司 一种新型苯并呋喃类衍生物、其制备方法和应用
CN113200947B (zh) * 2021-05-11 2022-11-15 广州医科大学 苯并呋喃类化合物及其应用

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3947470A (en) * 1974-06-20 1976-03-30 Smithkline Corporation Substituted benzofurans and benzothiophenes
US4024273A (en) * 1974-06-20 1977-05-17 Smithkline Corporation Coronary vasodilator and anti-anginal compositions comprising substituted benzofurans and benzothiophenes and methods of producing coronary vasodilation and anti-anginal activity
FI61030C (fi) * 1976-02-19 1982-05-10 Sanofi Sa Foerfarande foer framstaellning av terapeutiskt verkande 2-substituerade-1- eller 3-benzoyl-indolizinderivat
US4117128A (en) * 1976-08-03 1978-09-26 Smithkline Corporation Sulfonyl benzofurans and benzothiophenes having coronary vasodilator activity
US4520026A (en) * 1981-02-06 1985-05-28 S. A. Labaz N.V. Indolizine derivatives and use as cardiovascular agents
EP0094744A1 (en) * 1982-04-23 1983-11-23 Beecham Group Plc Azabicyclobenzamides, their preparation and their pharmaceutical compositions
US4567270A (en) * 1984-09-17 1986-01-28 G. D. Searle & Co. Hexahydroindolizinones useful for treating cardiac arrhythmia, thrombotic disorders in mammals
FR2594438B1 (fr) * 1986-02-14 1990-01-26 Labaz Sanofi Nv Derives d'indolizine, leur procede de preparation ainsi que les compositions en contenant
US4851554A (en) * 1987-04-06 1989-07-25 University Of Tennessee Research Corporation Certain 3-substituted 2-alkyl benzofuran derivatives
US4831156A (en) * 1987-09-30 1989-05-16 The University Of Tennessee Research Corp. 3-substituted 2-alkyl indole derivatives
AU2543388A (en) * 1987-09-30 1989-04-18 University Of Tennessee Research Corporation, The Certain 3-substituted 2-alkyl benzothiophene derivatives
US4831054A (en) * 1988-04-18 1989-05-16 Taro Pharmaceuticals, Ltd. 2-Alkyl-3-benzoylbenzofurans useful for treating cardiac arrhythmia
FR2633622B1 (fr) * 1988-07-04 1991-05-17 Sanofi Sa Derives de sulfonyl indolizine, leur procede de preparation et leur utilisation comme intermediaires de synthese
AT391316B (de) * 1988-09-15 1990-09-25 Ebewe Arzneimittel Neue thienyloxy-alkylamin-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
FR2642755B1 (sh) * 1989-02-07 1993-11-05 Sanofi

Also Published As

Publication number Publication date
KR920004371A (ko) 1992-03-27
NZ239232A (en) 1993-10-26
AU8142891A (en) 1992-02-13
ZA915934B (en) 1993-03-31
PL168044B1 (pl) 1995-12-30
MA22249A1 (fr) 1992-04-01
PT98576A (pt) 1992-06-30
IE912595A1 (en) 1992-02-12
FR2665444A1 (fr) 1992-02-07
TNSN91070A1 (fr) 1992-10-25
AU648569B2 (en) 1994-04-28
HU211656A9 (en) 1995-12-28
NO179042B (no) 1996-04-15
RU2095357C1 (ru) 1997-11-10
KR100190673B1 (ko) 1999-06-01
YU134891A (sh) 1994-01-20
CZ288527B6 (cs) 2001-07-11
SK283527B6 (sk) 2003-09-11
IL98991A (en) 1995-12-08
CA2047773A1 (en) 1992-02-07
NO913033L (no) 1992-02-07
EP0471609B1 (fr) 1996-11-27
CA2047773C (en) 2000-09-12
HUT62280A (en) 1993-04-28
FI913704A (fi) 1992-02-07
HU912610D0 (en) 1992-01-28
FI913704A0 (fi) 1991-08-02
FI114914B (fi) 2005-01-31
HU218271B (en) 2000-07-28
PT98576B (pt) 1999-01-29
JP2795759B2 (ja) 1998-09-10
CS242791A3 (en) 1992-03-18
PL291334A1 (en) 1992-10-19
JPH04316554A (ja) 1992-11-06
MY107655A (en) 1996-05-30
NO179042C (no) 1996-07-24
DK0471609T3 (da) 1997-05-26
TW199095B (sh) 1993-02-01
ATE145645T1 (de) 1996-12-15
EP0471609A1 (fr) 1992-02-19
NO913033D0 (no) 1991-08-05
US5223510A (en) 1993-06-29
HK1000108A1 (en) 1997-11-28
DE69123304T2 (de) 1997-06-12
IL98991A0 (en) 1992-07-15
OA09513A (fr) 1992-11-15
GR3022593T3 (en) 1997-05-31
SG49205A1 (en) 1998-05-18
FR2665444B1 (fr) 1992-11-27
DE69123304D1 (de) 1997-01-09
ES2096639T3 (es) 1997-03-16
BR9103354A (pt) 1992-05-05

Similar Documents

Publication Publication Date Title
YU48714B (sh) Derivati benzofurana, benzotiofena, indola i indolizina i postupak za njihovo dobijanje
ES8503675A1 (es) Procedimiento para la preparacion de nuevas n-alcoxi y n-alquil-sulfonilaminosulfonilureas
ES8604536A1 (es) Procedimiento para la preparacion de derivados de furazano
ES8404990A1 (es) Un procedimiento para la preparacion de derivados de prolina.
PT84144A (en) Process for preparing heterocyclic sulphonamides useful as antiallergic and antithrombotic agents
ES8601978A1 (es) Procedimiento para preparar derivados de isoquinoleina
DK221280A (da) 1-phenyl-2-aminoethanolderivater
NZ224956A (en) Benzo-thieno-thiazine derivatives, pharmaceuticals and intermediates
MX9708422A (es) Esteres de carbapenemas.
NO930844L (no) 2-(2-substituerte pyrrolidinyltio)karbapenem-derivater
SE7706441L (sv) Triazolylfenylketonderivat och framstellning derav
HUP0202237A2 (hu) Amin, módosított pszeudomicin vegyületek, azokat tartalmazó gyógyászati készítmény és alkalmazásuk
TW336883B (en) 2-substituted benzohydroxymoyl derivatives, intermediates for production and an active ingredient as a pesticide thereof
IT1230754B (it) Camposti con attivita' analgesica centrale.