ES8500273A1 - Un procedimiento para preparar pirazolo (4,3-c)piridinas. - Google Patents

Un procedimiento para preparar pirazolo (4,3-c)piridinas.

Info

Publication number
ES8500273A1
ES8500273A1 ES519832A ES519832A ES8500273A1 ES 8500273 A1 ES8500273 A1 ES 8500273A1 ES 519832 A ES519832 A ES 519832A ES 519832 A ES519832 A ES 519832A ES 8500273 A1 ES8500273 A1 ES 8500273A1
Authority
ES
Spain
Prior art keywords
pyridines
pharmacologically active
pyrazolo
active pyrazolo
neuroleptic
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
ES519832A
Other languages
English (en)
Other versions
ES519832A0 (es
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gruppo Lepetit SpA
Original Assignee
Gruppo Lepetit SpA
Lepetit SpA
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 Gruppo Lepetit SpA, Lepetit SpA filed Critical Gruppo Lepetit SpA
Publication of ES519832A0 publication Critical patent/ES519832A0/es
Publication of ES8500273A1 publication Critical patent/ES8500273A1/es
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D211/74—Oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Anesthesiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

PROCEDIMIENTO PARA LA OBTENCION DE PIRAZOLO4,3-CPIRIDINAS, Y DE SUS SALES DE ADICION DE ACIDO FISIOLOGICAMENTE COMPATIBLES, DE FORMULA (I), EN LA QUE R, R1 Y AR PUEDEN SER VARIOS RADICALES.CONSISTE EN LA REACCION DE UN COMPUESTO DE FORMULA (II), EN LA QUE R Y AR TIENEN EL MISMO SIGNIFICADO QUE EN LA FORMULA (I), CON HIDRATO DE HIDRAZINA CONCENTRADO. LA TEMPERATURA SE MANTIENE A 0JC DURANTE LA ADICION Y POSTERIORMENTE SE AUMENTA HASTA LA TEMPERATURA AMBIENTE, O ALGO SUPERIOR.ESTOS COMPUESTOS TIENEN APLICACIONES FARMACOLOGICAS COMO AGENTES DEPRESORES DEL SISTEMA NERVIOSO CENTRAL, NEUROLEPTICOS, CARDIOTONICOS, ANTIHIPERTENSORES, ANALGESICOS Y ANTIINFLAMATORIOS.
ES519832A 1982-02-17 1983-02-16 Un procedimiento para preparar pirazolo (4,3-c)piridinas. Expired ES8500273A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8204722 1982-02-17

Publications (2)

Publication Number Publication Date
ES519832A0 ES519832A0 (es) 1984-10-01
ES8500273A1 true ES8500273A1 (es) 1984-10-01

Family

ID=10528419

Family Applications (3)

Application Number Title Priority Date Filing Date
ES519832A Expired ES8500273A1 (es) 1982-02-17 1983-02-16 Un procedimiento para preparar pirazolo (4,3-c)piridinas.
ES531980A Granted ES531980A0 (es) 1982-02-17 1984-04-27 Un procedimiento para preparar pirazolo (4,3-c) piridinas
ES531981A Expired ES8507547A1 (es) 1982-02-17 1984-04-27 Un procedimiento para preparar pirazolo (4,3-c) piridinas

Family Applications After (2)

Application Number Title Priority Date Filing Date
ES531980A Granted ES531980A0 (es) 1982-02-17 1984-04-27 Un procedimiento para preparar pirazolo (4,3-c) piridinas
ES531981A Expired ES8507547A1 (es) 1982-02-17 1984-04-27 Un procedimiento para preparar pirazolo (4,3-c) piridinas

Country Status (16)

Country Link
US (1) US4500525A (es)
EP (1) EP0086422B1 (es)
JP (1) JPS58152885A (es)
KR (1) KR900006853B1 (es)
AT (1) ATE30027T1 (es)
AU (1) AU563591B2 (es)
CA (1) CA1225646A (es)
DE (1) DE3373904D1 (es)
DK (1) DK27383A (es)
ES (3) ES8500273A1 (es)
GR (1) GR78080B (es)
IE (1) IE55156B1 (es)
IL (1) IL67785A0 (es)
NZ (1) NZ203302A (es)
PH (1) PH23645A (es)
ZA (1) ZA83628B (es)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5137890A (en) * 1990-02-14 1992-08-11 Ortho Pharmaceutical Corporation 4-phenyl tetrahydropyrido(4,3-d)pyrimidines
US5264576A (en) * 1992-10-22 1993-11-23 Hoechst-Roussel Pharmaceuticals Incorporated Pyrazolo[4,3-c]pyridines which are intermediates
DE19834044A1 (de) 1998-07-29 2000-02-03 Bayer Ag Neue substituierte Pyrazolderivate
DE60126286T2 (de) * 2000-08-14 2007-11-15 Ortho-Mcneil Pharmaceutical, Inc. Substituierte pyrazole
US20070105841A1 (en) * 2000-08-14 2007-05-10 Breitenbucher J G Method for treating allergies using substituted pyrazoles
US7332494B2 (en) 2000-08-14 2008-02-19 Janssen Pharmaceutica, N.V. Method for treating allergies using substituted pyrazoles
AU2001284823B2 (en) 2000-08-14 2006-11-30 Ortho-Mcneil Pharmaceutical, Inc. Substituted pyrazoles
EP1309593B1 (en) 2000-08-14 2006-03-15 Ortho-McNeil Pharmaceutical, Inc. Substituted pyrazoles
US20050101587A9 (en) * 2000-08-14 2005-05-12 Butler Christopher R. Method for treating allergies using substituted pyrazoles
US20070117785A1 (en) * 2000-08-14 2007-05-24 Butler Christopher R Substituted pyrazoles and methods of treatment with substituted pyrazoles
AU2001288714A1 (en) 2000-09-06 2002-03-22 Ortho-Mcneil Pharmaceutical, Inc. A method for treating allergies
JP2004508329A (ja) * 2000-09-06 2004-03-18 オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド 置換ピラゾールを使用するアレルギーの処置法
PL374023A1 (en) * 2002-05-30 2005-09-19 Vertex Pharmaceuticals Incorporated Inhibitors of jak and cdk2 protein kinases
CA2493625A1 (en) * 2002-07-25 2004-02-19 Pharmacia Italia S.P.A. Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
EP2243781A1 (en) * 2003-05-30 2010-10-27 Vertex Pharmaceuticals, Inc. Pyrazolopyridine derivatives as inhibitors of JAK and CDK2 protein kinases
DK1668014T3 (da) 2003-09-17 2009-04-20 Janssen Pharmaceutica Nv Kondenserede heterocykliske forbindelser som serotoninreceptormodulatorer
ATE546452T1 (de) 2003-09-23 2012-03-15 Vertex Pharma Pyrazolopyrrolderivate als proteinkinaseinhibitoren
KR100838692B1 (ko) 2007-07-11 2008-06-16 한국화학연구원 7-(3′,4′-디알콕시페닐)-4,5,6,7-테트라히드로피라졸로[1,5-ａ]피리미딘 화합물, 이의 제조방법 및 이를 포함하는천식 및 만성폐쇄성 폐질환을 포함한 염증관련 질환,관절염, 아토피 피부염, 암 및 뇌질환의 치료 및 예방을위한 약제학적 조성물
US9242981B2 (en) 2010-09-16 2016-01-26 Merck Sharp & Dohme Corp. Fused pyrazole derivatives as novel ERK inhibitors
EA023648B1 (ru) * 2011-09-12 2016-06-30 Санофи ИНДАНИЛЗАМЕЩЕННЫЕ 4,5,6,7-ТЕТРАГИДРО-1H-ПИРАЗОЛО[4,3-с]ПИРИДИНЫ, ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ЛЕКАРСТВЕННОГО СРЕДСТВА И СОДЕРЖАЩИЕ ИХ ФАРМАЦЕВТИЧЕСКИЕ ПРЕПАРАТЫ
SI2755972T1 (sl) 2011-09-12 2016-02-29 Sanofi Indanil-substituirani 4,5,6,7-tetrahidro-1H-pirazolo(4,3-c)piridini, njihova uporaba kot zdravilo in farmacevtski pripravki, ki jih vsebujejo
CA2846366A1 (en) 2011-09-16 2013-03-21 Sanofi Substituted 4,5,6,7-tetrahydro-1h-pyrazolo[4,3-c]pyridines, their use as medicament, and pharmaceutical preparations comprising them
WO2013037914A1 (en) 2011-09-16 2013-03-21 Sanofi Substituted 4,5,6,7-tetrahydro-1h-pyrazolo[4,3-c]pyridines, their use as medicament, and pharmaceutical preparations comprising them
JP6713465B2 (ja) 2014-12-30 2020-06-24 ノヴィラ・セラピューティクス・インコーポレイテッド Ｂ型肝炎感染症治療のための誘導体及び方法
JP7014736B2 (ja) * 2016-05-24 2022-02-01 ジェネンテック， インコーポレイテッド がんの処置のためのピラゾロピリジン誘導体
AU2017286890B2 (en) 2016-06-29 2021-09-09 Novira Therapeutics, Inc. Oxadiazepinone derivatives and their use in the treatment of hepatitis B infections
WO2018005883A1 (en) 2016-06-29 2018-01-04 Novira Therapeutics, Inc. Diazepinone derivatives and their use in the treatment of hepatitis b infections
WO2018222598A1 (en) 2017-05-31 2018-12-06 Chemocentryx, Inc. 6-5 FUSED RINGS AS C5a INHIBITORS
EP3728203B1 (en) * 2017-12-22 2024-03-13 ChemoCentryx, Inc. DIARYL SUBSTITUTED 6,5-FUSED RING COMPOUNDS AS C5aR INHIBITORS

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3852279A (en) * 1973-03-12 1974-12-03 Squibb & Sons Inc 7-substituted -3,3a,4,5,6,7-hexahydro-3-substituted-2h- pyrazolo (4,3-c)pyridines

Also Published As

Publication number Publication date
US4500525A (en) 1985-02-19
KR900006853B1 (ko) 1990-09-22
IE55156B1 (en) 1990-06-20
DK27383A (da) 1983-08-18
KR840003636A (ko) 1984-09-15
ES519832A0 (es) 1984-10-01
ATE30027T1 (de) 1987-10-15
AU1130583A (en) 1983-08-25
AU563591B2 (en) 1987-07-16
NZ203302A (en) 1986-08-08
JPH0412269B2 (es) 1992-03-04
ES8507546A1 (es) 1985-09-01
EP0086422A3 (en) 1984-03-28
PH23645A (en) 1989-09-27
ZA83628B (en) 1983-12-28
ES531980A0 (es) 1985-09-01
EP0086422B1 (en) 1987-09-30
ES531981A0 (es) 1985-09-01
IL67785A0 (en) 1983-05-15
DK27383D0 (da) 1983-01-25
ES8507547A1 (es) 1985-09-01
GR78080B (es) 1984-09-26
IE830328L (en) 1983-08-17
DE3373904D1 (en) 1987-11-05
JPS58152885A (ja) 1983-09-10
EP0086422A2 (en) 1983-08-24
CA1225646A (en) 1987-08-18

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19970303