AP830A - Indole derivatives useful in therapy. - Google Patents

Indole derivatives useful in therapy. Download PDF

Info

Publication number
AP830A
AP830A APAP/P/1997/000982A AP9700982A AP830A AP 830 A AP830 A AP 830A AP 9700982 A AP9700982 A AP 9700982A AP 830 A AP830 A AP 830A
Authority
AP
ARIPO
Prior art keywords
alkyl
formula
reaction
independently represent
compound
Prior art date
Application number
APAP/P/1997/000982A
Other languages
English (en)
Other versions
AP9700982A0 (en
Inventor
David James Rawson
Kevin Neil Dack
Roger Peter Dickinson
Kim James
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of AP9700982A0 publication Critical patent/AP9700982A0/xx
Application granted granted Critical
Publication of AP830A publication Critical patent/AP830A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • A61P9/10Drugs 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
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Pulmonology (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
APAP/P/1997/000982A 1996-05-09 1997-05-08 Indole derivatives useful in therapy. AP830A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9609641.7A GB9609641D0 (en) 1996-05-09 1996-05-09 Compounds useful in therapy

Publications (2)

Publication Number Publication Date
AP9700982A0 AP9700982A0 (en) 1997-07-31
AP830A true AP830A (en) 2000-05-03

Family

ID=10793387

Family Applications (1)

Application Number Title Priority Date Filing Date
APAP/P/1997/000982A AP830A (en) 1996-05-09 1997-05-08 Indole derivatives useful in therapy.

Country Status (43)

Country Link
US (4) US6017945A (is)
EP (1) EP0901470B1 (is)
JP (1) JP3245179B2 (is)
KR (1) KR100331217B1 (is)
CN (1) CN1124262C (is)
AP (1) AP830A (is)
AR (1) AR007030A1 (is)
AT (1) ATE263151T1 (is)
AU (1) AU717849B2 (is)
BG (1) BG102873A (is)
BR (1) BR9709072A (is)
CA (1) CA2253876A1 (is)
CO (1) CO4650036A1 (is)
CZ (1) CZ292928B6 (is)
DE (1) DE69728392T2 (is)
DK (1) DK0901470T3 (is)
DZ (1) DZ2227A1 (is)
EA (1) EA001471B1 (is)
ES (1) ES2218675T3 (is)
GB (1) GB9609641D0 (is)
HK (1) HK1019149A1 (is)
HN (1) HN1997000058A (is)
HR (1) HRP970249B1 (is)
HU (1) HUP9901245A3 (is)
ID (1) ID16878A (is)
IL (1) IL125903A0 (is)
IS (1) IS1856B (is)
MA (1) MA26428A1 (is)
NO (1) NO312547B1 (is)
NZ (1) NZ332640A (is)
OA (1) OA10896A (is)
PE (1) PE65098A1 (is)
PL (1) PL329725A1 (is)
PT (1) PT901470E (is)
SI (1) SI0901470T1 (is)
SK (1) SK150398A3 (is)
TN (1) TNSN97078A1 (is)
TR (1) TR199802269T2 (is)
TW (1) TW491838B (is)
UA (1) UA50767C2 (is)
UY (1) UY24546A1 (is)
WO (1) WO1997043260A1 (is)
ZA (1) ZA973963B (is)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9722287D0 (en) 1997-10-22 1997-12-17 Pfizer Ltd Compounds useful in therapy
AU763618B2 (en) 1999-02-10 2003-07-31 Astrazeneca Ab Quinazoline derivatives as angiogenesis inhibitors
US20050203166A1 (en) * 2000-06-30 2005-09-15 Cancer Research Technology Limited Indole-3-acetic acid derivatives
GB0016162D0 (en) * 2000-06-30 2000-08-23 Cancer Res Campaign Tech Indole-3-acetic acid derivatives
TWI224101B (en) 2001-06-20 2004-11-21 Wyeth Corp Substituted naphthyl indole derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1)
JP4399253B2 (ja) 2001-06-20 2010-01-13 ワイス プラスミノゲンアクチベーターインヒビター−1(pai−1)のインヒビターとしての、置換されたインドール酸誘導体
AR037097A1 (es) 2001-10-05 2004-10-20 Novartis Ag Compuestos acilsulfonamidas, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento
ATE430731T1 (de) 2002-12-10 2009-05-15 Wyeth Corp Substituierte indoloxoacetylaminoessigsäurederivate als inhibitoren des plasminogenaktivatorinhibitors-1 (pai-1)
UA80453C2 (en) 2002-12-10 2007-09-25 Derivatives of substituted dyhydropyranoindol-3,4-dion as inhibitors of plasminogen activator inhibitor-1 (pai-1)
ATE331709T1 (de) 2002-12-10 2006-07-15 Wyeth Corp Substituierte 3-carbonyl-1-yl essigsäure derivate als plasminogen aktivator inhibitor(pai-1) inhibitoren
US7259182B2 (en) 2002-12-10 2007-08-21 Wyeth Aryl, aryloxy, and aklyloxy substituted 1H-indol-3-yl glyoxylic acid derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)
BR0316583A (pt) 2002-12-10 2005-10-04 Wyeth Corp Derivados de ácido acético 3-alquil e 3-arilalquil 1h-indol-1-il substituìdo como inibidores do inibidor-1 do ativador do plasminogênio (pai-1)
BRPI0406883A (pt) * 2003-01-22 2006-01-03 Lilly Co Eli Composto, composição farmacêutica, método de tratar um distúrbio, e, uso de um composto
US7351726B2 (en) 2003-09-25 2008-04-01 Wyeth Substituted oxadiazolidinediones
US7332521B2 (en) 2003-09-25 2008-02-19 Wyeth Substituted indoles
US7420083B2 (en) 2003-09-25 2008-09-02 Wyeth Substituted aryloximes
US7141592B2 (en) 2003-09-25 2006-11-28 Wyeth Substituted oxadiazolidinediones
US7265148B2 (en) 2003-09-25 2007-09-04 Wyeth Substituted pyrrole-indoles
US7582773B2 (en) 2003-09-25 2009-09-01 Wyeth Substituted phenyl indoles
US7446201B2 (en) 2003-09-25 2008-11-04 Wyeth Substituted heteroaryl benzofuran acids
US7163954B2 (en) 2003-09-25 2007-01-16 Wyeth Substituted naphthyl benzothiophene acids
US7442805B2 (en) 2003-09-25 2008-10-28 Wyeth Substituted sulfonamide-indoles
US7411083B2 (en) 2003-09-25 2008-08-12 Wyeth Substituted acetic acid derivatives
US7342039B2 (en) 2003-09-25 2008-03-11 Wyeth Substituted indole oximes
US7268159B2 (en) 2003-09-25 2007-09-11 Wyeth Substituted indoles
JP2005109006A (ja) * 2003-09-29 2005-04-21 Tdk Corp 高電圧貫通型コンデンサ及びマグネトロン
HN2004000536A (es) * 2003-12-16 2009-02-18 Wyeth Corp Un procediemiento de sintesis para la alquilacion reductiva de la posicon c-3 de indoles
MX2007002178A (es) 2004-08-23 2007-04-02 Wyeth Corp Acidos de oxazolo-naftilo como moduladores del inhibidor del activador de plasminogeno tipo 1 (pai-1) util en el tratamiento de trombosis y enfermedades cardiovasculares.
WO2007022321A2 (en) 2005-08-17 2007-02-22 Wyeth Substituted indoles and use thereof
BRPI0709950A2 (pt) * 2006-04-13 2011-08-02 Actelion Pharmaceuticals Ltd uso de bosentan na preparação de um medicamento para o tratamento de fibrose pulmonar idiopática em estágio precoce e uso de antagonista do receptor endotelin
DE102008030207A1 (de) 2008-06-25 2009-12-31 Bayer Schering Pharma Aktiengesellschaft Substituierte 7-Sulfanylmethyl-, 7-Sulfinylmethyl- und 7-Sulfonylmethyl-Indole und ihre Verwendung
DE102008030206A1 (de) 2008-06-25 2009-12-31 Bayer Schering Pharma Aktiengesellschaft 3-Cyanoalky- und 3-Hydroxyalkyl-Indole und ihre Verwendung
CN106674065A (zh) * 2016-12-07 2017-05-17 贵州大学 一种5‑卤代‑2‑烷氧基‑4‑甲苯磺酰氯制备方法
GB201817038D0 (en) * 2018-10-19 2018-12-05 Inflazome Ltd Novel processes
BR112021016620A2 (pt) 2019-02-27 2021-11-03 Univ California Azepino-indóis e outros heterociclos para o tratamento de distúrbios cerebrais

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994014434A1 (en) * 1992-12-22 1994-07-07 Smithkline Beecham Corporation Endothelin receptor antagonists
EP0617001A1 (en) * 1993-03-19 1994-09-28 Merck & Co. Inc. Phenoxyphenylacetic acid derivatives

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE637353A (is) * 1962-09-14
DE1950346B2 (de) * 1968-10-08 1973-06-28 Sumitomo Chemical Co 2-indolylessigsaeureverbindungen und diese verbindungen enthaltende arzneipraeparate
US4397079A (en) * 1981-03-30 1983-08-09 International Business Machines Corp. Process for improving the yield of integrated devices including Schottky barrier diodes
US5245046A (en) * 1988-11-14 1993-09-14 The Upjohn Company α-amino-indole-3-acetic acids useful as anti-diabetic, anti-obesity and anti-atherosclerotic agents
AU8641991A (en) * 1990-09-10 1992-03-30 Rhone-Poulenc Rorer International (Holdings) Inc. Substituted bicyclic aryl compounds exhibiting selective leukotriene b4 antagonist activity
GB9317096D0 (en) * 1993-08-17 1993-09-29 Pfizer Ltd Indoles

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994014434A1 (en) * 1992-12-22 1994-07-07 Smithkline Beecham Corporation Endothelin receptor antagonists
EP0617001A1 (en) * 1993-03-19 1994-09-28 Merck & Co. Inc. Phenoxyphenylacetic acid derivatives

Also Published As

Publication number Publication date
HUP9901245A2 (hu) 1999-08-30
AU2697897A (en) 1997-12-05
TR199802269T2 (xx) 2001-12-21
HN1997000058A (es) 1997-06-26
US6017945A (en) 2000-01-25
EA199800908A1 (ru) 1999-06-24
AR007030A1 (es) 1999-10-13
IS4838A (is) 1998-08-28
UY24546A1 (es) 2000-09-29
GB9609641D0 (en) 1996-07-10
KR20000010879A (ko) 2000-02-25
KR100331217B1 (ko) 2002-05-09
CO4650036A1 (es) 1998-09-03
UA50767C2 (uk) 2002-11-15
US6136843A (en) 2000-10-24
CN1216531A (zh) 1999-05-12
MA26428A1 (fr) 2004-12-20
HRP970249A2 (en) 1998-06-30
HK1019149A1 (en) 2000-01-14
PE65098A1 (es) 1998-10-29
US6306852B1 (en) 2001-10-23
JPH11508285A (ja) 1999-07-21
CN1124262C (zh) 2003-10-15
NO985225L (no) 1998-11-09
CA2253876A1 (en) 1997-11-20
ES2218675T3 (es) 2004-11-16
TNSN97078A1 (fr) 2005-03-15
WO1997043260A1 (en) 1997-11-20
PT901470E (pt) 2004-07-30
IS1856B (is) 2003-02-21
HUP9901245A3 (en) 2002-01-28
NZ332640A (en) 2001-03-30
DE69728392T2 (de) 2005-01-13
NO985225D0 (no) 1998-11-09
ATE263151T1 (de) 2004-04-15
SI0901470T1 (en) 2004-08-31
EP0901470B1 (en) 2004-03-31
TW491838B (en) 2002-06-21
EP0901470A1 (en) 1999-03-17
DZ2227A1 (fr) 2002-12-25
BG102873A (en) 1999-11-30
SK150398A3 (en) 1999-03-12
DK0901470T3 (da) 2004-07-12
PL329725A1 (en) 1999-04-12
EA001471B1 (ru) 2001-04-23
CZ358298A3 (cs) 1999-08-11
US6384070B2 (en) 2002-05-07
OA10896A (en) 2001-10-11
AP9700982A0 (en) 1997-07-31
IL125903A0 (en) 1999-04-11
ZA973963B (en) 1998-11-09
US20010014677A1 (en) 2001-08-16
BR9709072A (pt) 1999-08-03
CZ292928B6 (cs) 2004-01-14
ID16878A (id) 1997-11-20
HRP970249B1 (en) 2003-06-30
AU717849B2 (en) 2000-04-06
DE69728392D1 (de) 2004-05-06
JP3245179B2 (ja) 2002-01-07
NO312547B1 (no) 2002-05-27

Similar Documents

Publication Publication Date Title
AP830A (en) Indole derivatives useful in therapy.
Hewawasam et al. A general method for the synthesis of isatins: preparation of regiospecifically functionalized isatins from anilines
Wang et al. Facile synthesis of 3, 3-di (heteroaryl) indolin-2-one derivatives catalyzed by ceric ammonium nitrate (CAN) under ultrasound irradiation
JP2638752B2 (ja) 1−アミノエチルインドール誘導体
EP0079564B1 (en) 3-(1-substituted-4-piperidyl)-1,2-benzisoxazoles, a process for the preparation thereof, a pharmaceutical composition comprising the same, and their use as medicaments
US2814625A (en) 3-indolyl amino hydrocarbyl ketones
Powers Chloroindoles1
US6355642B1 (en) Tetrahydrobenzindole compounds
Adamek et al. 1-Imidoalkylphosphonium salts with modulated Cα–P+ bond strength: synthesis and application as new active α-imidoalkylating agents
AU600813B2 (en) Aliphatic carboxamides
US4837235A (en) Indole and indazole keto sulphones as leukotriene antagonists
DE69107064T2 (de) Indolderivate.
Acheson 1-Hydroxypyrroles, 1-hydroxyindoles and 9-hydroxycarbazoles
Walser et al. Synthesis and transformations of some 3-chloro-and 3-nitroindolenines
EP0432648B1 (en) Isatine derivatives, their preparation and use
MURAKAMI et al. Fischer indolization of ethyl pyruvate 2-[2-(trifluoromethyl) phenyl]-phenylhydrazone and new insight into the mechanism of the Goldberg reaction.(Fischer indolization and its related compounds. XXVI)
US6326501B1 (en) Methylation of indole compounds using dimethyl carbonate
JPH02188579A (ja) インドリルイミダゾール誘導体
JP2585341B2 (ja) アルキルメラトニン類
Black et al. Synthesis and reactivity of 1-pyrroline-5-carboxylate ester 1-oxides
US2930797A (en) 2-alkyl-3-indoleglyoxylamides
Volk et al. New One‐Pot Synthesis of 3‐Alkyl‐and 3‐(ψ‐Hydroxyalkyl) oxindoles from Isatins
Flury et al. 2, 2, 2‐Trifluoroethanol‐mediated hydroarylation of fluorinated alkynes with indoles: Application to diindolylmethanes
HU192416B (en) Process for preparing indole derivatives and pharmaceutical compositions containing sucg compounds
US3037991A (en) 3-endolyl-2-aminoethylketones and their preparation