ES8707932A1 - Un procedimiento para la preparacion de esteres del acido 1,4-dihidro-3,5, piridincarboxilico. - Google Patents

Un procedimiento para la preparacion de esteres del acido 1,4-dihidro-3,5, piridincarboxilico.

Info

Publication number
ES8707932A1
ES8707932A1 ES552051A ES552051A ES8707932A1 ES 8707932 A1 ES8707932 A1 ES 8707932A1 ES 552051 A ES552051 A ES 552051A ES 552051 A ES552051 A ES 552051A ES 8707932 A1 ES8707932 A1 ES 8707932A1
Authority
ES
Spain
Prior art keywords
alkyl
straight
formula
independently represent
calcium ion
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
ES552051A
Other languages
English (en)
Other versions
ES552051A0 (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.)
GlaxoSmithKline SpA
Original Assignee
Glaxo 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
Priority claimed from IT22383/84A external-priority patent/IT1175620B/it
Priority claimed from IT21460/85A external-priority patent/IT1187678B/it
Application filed by Glaxo SpA filed Critical Glaxo SpA
Publication of ES8707932A1 publication Critical patent/ES8707932A1/es
Publication of ES552051A0 publication Critical patent/ES552051A0/es
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07D211/80—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 two double bonds between ring members or between ring members and non-ring members
    • C07D211/84—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 two double bonds between ring members or between ring members and non-ring members 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
    • C07D211/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • 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
    • 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
    • A61P9/08—Vasodilators for multiple indications
    • 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
    • A61P9/10—Drugs 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
    • 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
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2205/00—Fibre drawing or extruding details
    • C03B2205/44—Monotoring or regulating the preform feed rate

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

METODO DE PREPARAR ESTERES DEL ACIDO 1,4-DIHIDRO-3,5-PIRIDINDICARBOXILICO. CONSISTE EN HACER REACCIONAR UN COMPUESTO DE FORMULA (II) CON UN TRIFENILFOSFORANO DE FORMULA (III), EN TETRAHIDROFURANO Y ENTRE 40 Y 120JC, PARA OBTENER UN COMPUESTO DE FORMULA (I), SIENDO R1 Y R4, INDEPENDIENTEMENTE, UN GRUPO ALQUILO DE C 1 A 4; R2 Y R3, INDEPENDIENTEMENTE, UN GRUPO ALQUILO DE C 1 A 6 LINEAL INTERCAMBIABLE POR HAL; Y R5 UN GRUPO ALQUILO DE C 1 A 13 DE CADA LINEAL, UN GRUPO CICLOALQUILO DE C 5 A 8 Y OTROS. SE UTILIZAN PARA TRATAR LA HIPERTENSION.-
ES552051A 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4-dihidro-3,5, piridincarboxilico. Expired ES8707932A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT22383/84A IT1175620B (it) 1984-08-22 1984-08-22 Derivati piridinici
IT21460/85A IT1187678B (it) 1985-07-05 1985-07-05 Procedimento di preparazione di derivati eterociclici

Publications (2)

Publication Number Publication Date
ES8707932A1 true ES8707932A1 (es) 1987-09-01
ES552051A0 ES552051A0 (es) 1987-09-01

Family

ID=26327905

Family Applications (5)

Application Number Title Priority Date Filing Date
ES546324A Expired ES8703839A1 (es) 1984-08-22 1985-08-21 Un procedimiento para la preparacion de esteres de acidos 1,4-dihidro-3,5-piridin-dicarbaxolicos.
ES552050A Expired ES8707930A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4-dihidro-3, 5, piridincarboxilico.
ES552048A Expired ES8707931A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4, dihidro-3,5-piridincarboxilico.
ES552049A Expired ES8802497A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4-dihidro -3,5-piridindi-carboxilico.
ES552051A Expired ES8707932A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4-dihidro-3,5, piridincarboxilico.

Family Applications Before (4)

Application Number Title Priority Date Filing Date
ES546324A Expired ES8703839A1 (es) 1984-08-22 1985-08-21 Un procedimiento para la preparacion de esteres de acidos 1,4-dihidro-3,5-piridin-dicarbaxolicos.
ES552050A Expired ES8707930A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4-dihidro-3, 5, piridincarboxilico.
ES552048A Expired ES8707931A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4, dihidro-3,5-piridincarboxilico.
ES552049A Expired ES8802497A1 (es) 1984-08-22 1986-02-14 Un procedimiento para la preparacion de esteres del acido 1,4-dihidro -3,5-piridindi-carboxilico.

Country Status (33)

Country Link
US (2) US4801599A (es)
JP (2) JPS6193162A (es)
KR (1) KR920004482B1 (es)
AT (1) AT394042B (es)
AU (1) AU578724B2 (es)
BE (1) BE903103A (es)
BG (1) BG60409B2 (es)
CA (1) CA1268180A (es)
CH (1) CH666684A5 (es)
CS (1) CS403091A3 (es)
CY (1) CY1494A (es)
DE (1) DE3529997C2 (es)
DK (1) DK165949C (es)
ES (5) ES8703839A1 (es)
FI (1) FI81568C (es)
FR (1) FR2569402B1 (es)
GB (1) GB2164336B (es)
GR (1) GR852016B (es)
HK (1) HK52990A (es)
HU (1) HU196754B (es)
IE (1) IE58486B1 (es)
LU (2) LU86047A1 (es)
MX (1) MX159974A (es)
NL (2) NL193065C (es)
NO (2) NO167142C (es)
NZ (1) NZ212895A (es)
PH (1) PH22014A (es)
PT (1) PT81000B (es)
SA (1) SA91120277B1 (es)
SE (1) SE459920B (es)
SG (1) SG40889G (es)
SK (1) SK278327B6 (es)
ZW (1) ZW13185A1 (es)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ212895A (en) * 1984-08-22 1988-07-28 Glaxo Spa 1,4-dihydropyridine derivatives and pharmaceutical compositions
EP0226271B1 (en) * 1985-08-21 1990-11-22 GLAXO S.p.A. 1,4-dihydropyridine compounds and their preparation and pharmaceutical formulation
NZ217282A (en) * 1985-08-21 1989-01-27 Glaxo Spa 1,4-dihydropyridine derivatives and pharmaceutical compositions
IT1204460B (it) * 1986-02-20 1989-03-01 Glaxo Spa Derivati eterociclici
IT1204461B (it) * 1986-02-20 1989-03-01 Glaxo Spa Derivati eterociclici
IT1204462B (it) * 1986-02-20 1989-03-01 Glaxo Spa Derivati eterociclici
IT1233370B (it) * 1988-11-21 1992-03-27 Glaxo Spa Procedimento di preparazione di derivati diidropipiridinici utili nel trattamento di disturbi cardiovascolari
EP0395369B1 (en) 1989-04-27 1997-07-02 Canon Inc. Optical recording medium and process for production thereof
US5177202A (en) * 1990-10-09 1993-01-05 Merck & Co., Inc. 2-phenanthrenyl-carbapenems
US5196529A (en) * 1990-10-09 1993-03-23 Merck & Co., Inc. 2-phenanthrenyl carbapenem intermediates
US5132421A (en) * 1990-10-09 1992-07-21 Merck & Co., Inc. 2-naphthyl-carbapenem intermediates
US5132422A (en) * 1990-10-09 1992-07-21 Merck & Co., Inc. 2-naphthyl-carbapenem intermediates
US5144028A (en) * 1990-10-09 1992-09-01 Merck & Co., Inc. 2-(9-fluorenonyl)-carbapenem intermediates
US5356889A (en) * 1990-08-01 1994-10-18 Merck & Co., Inc. 2-(9-fluorenonyl)-carbapenem intermediates
US5208329A (en) * 1990-10-09 1993-05-04 Merck & Co., Inc. 2-biphenyl carbapenem intermediates
IT1244728B (it) * 1991-02-13 1994-08-08 Glaxo Spa Impiego medicamentoso di derivati diidropiridinici
TW483763B (en) * 1994-09-02 2002-04-21 Astra Ab Pharmaceutical composition comprising of ramipril and dihydropyridine compound
AU1042199A (en) * 1998-11-06 2000-05-29 Boehringer Ingelheim International Gmbh Antihypertensive medicaments containing lacidipine and telmisartan
CN1681495B (zh) 2002-08-19 2010-05-12 辉瑞产品公司 用于治疗过度增生性疾病的组合物
KR20110117731A (ko) * 2003-05-30 2011-10-27 랜박시 래보러터리스 리미티드 치환된 피롤 유도체와 ｈｍｇ―ｃｏ 억제제로서의 이의 용도
US20050037063A1 (en) * 2003-07-21 2005-02-17 Bolton Anthony E. Combined therapies
KR20070054644A (ko) * 2004-07-26 2007-05-29 액테리온 파마슈티칼 리미티드 미립자 제형으로 흡입된 일로프로스트에 의한 폐고혈압의치료
WO2006113309A1 (en) 2005-04-15 2006-10-26 Dr. Reddy's Laboratories Ltd. Lacidipine particles
US20070043088A1 (en) * 2005-08-16 2007-02-22 Eswaraiah Sajja Process for preparing lacidipine
US7741317B2 (en) 2005-10-21 2010-06-22 Bristol-Myers Squibb Company LXR modulators
EP2351569B1 (en) 2005-10-26 2012-08-22 Asahi Kasei Pharma Corporation Fasudil in combination therapies for the treatment of pulmonary arterial hypertension
ATE551059T1 (de) 2005-10-26 2012-04-15 Asahi Kasei Pharma Corp Fasudil in kombination mit bosentan zur behandlung von pulmonaler arterieller hypertonie
AU2006313430B2 (en) * 2005-11-08 2012-09-06 Ranbaxy Laboratories Limited Process for (3R,5R)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4- [(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3, 5-dihydroxy-heptanoic acid hemi calcium salt
US7888376B2 (en) 2005-11-23 2011-02-15 Bristol-Myers Squibb Company Heterocyclic CETP inhibitors
US7919506B2 (en) 2006-03-10 2011-04-05 Pfizer Inc. Dibenzyl amine compounds and derivatives
WO2008020314A2 (en) * 2006-03-14 2008-02-21 Ranbaxy Laboratories Limited Statin stabilizing dosage formulations
WO2008010087A2 (en) * 2006-07-14 2008-01-24 Ranbaxy Laboratories Limited Polymorphic forms of an hmg-coa reductase inhibitor and uses thereof
US20080089947A1 (en) * 2006-08-18 2008-04-17 Knox Clayton D Calcium Influx Inhibitors in the Treatment of Ischemia
JP5498168B2 (ja) 2006-12-01 2014-05-21 ブリストル−マイヤーズ スクイブ カンパニー アテローム性動脈硬化および循環器疾患の治療のためのｃｅｔｐ阻害剤としてのｎ−（（３−ベンジル）−２，２−（ビス−フェニル）−プロパン−１−アミン誘導体
WO2012037665A1 (en) 2010-09-24 2012-03-29 Oral Delivery Technology Ltd. Nitric oxide releasing amino acid ester for treatment of pulmonary hypertension and other respiratory conditions
PL2705839T3 (pl) 2012-09-10 2018-07-31 Rivopharm Sa Farmaceutyczna kompozycja zawierająca lacydypinę i proces przygotowania
EP2986599A1 (en) 2013-04-17 2016-02-24 Pfizer Inc. N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases
WO2016055901A1 (en) 2014-10-08 2016-04-14 Pfizer Inc. Substituted amide compounds
BR112021013807A2 (pt) 2019-01-18 2021-11-30 Astrazeneca Ab Inibidores de pcsk9 e seus métodos de uso

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Publication number Priority date Publication date Assignee Title
US3455945A (en) * 1967-06-07 1969-07-15 Smithkline Corp 4-(carboxy (and carbo-lower alkoxy)phenyl)-1,4-dihydropyridines
DE2228363A1 (de) * 1972-06-10 1974-01-03 Bayer Ag 1,4-dihydropyridine, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
GB1409865A (en) * 1973-02-13 1975-10-15 Science Union & Cie Dihydropyridines derivatives their preparation and pharmaceu tical compositions containing them
US4307103A (en) * 1978-09-08 1981-12-22 Fujisawa Pharmaceutical Co., Ltd. Dihydropyridine derivative, processes for preparation thereof and pharmaceutical composition comprising the same
DE3018259A1 (de) * 1980-05-13 1981-11-19 Bayer Ag, 5090 Leverkusen 1,4-dihydropyridine mit unterschiedlichen substituenten in 2- und 6-position, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln
NZ201395A (en) * 1981-07-30 1987-02-20 Bayer Ag Pharmaceutical compositions containing 1,4-dihydropyridines and certain of these dihydropyridines
DE3207982A1 (de) * 1982-03-05 1983-09-08 Bayer Ag, 5090 Leverkusen Neue 1,4-dihydropyridine, verfahren zu ihrer herstellung und ihrer verwendung in arzneimitteln
NZ212895A (en) * 1984-08-22 1988-07-28 Glaxo Spa 1,4-dihydropyridine derivatives and pharmaceutical compositions

Also Published As

Publication number Publication date
FI853206L (fi) 1986-02-23
ES8703839A1 (es) 1987-03-01
CA1268180A (en) 1990-04-24
DE3529997A1 (de) 1986-03-06
DK165949C (da) 1993-07-05
FI81568C (fi) 1990-11-12
BE903103A (fr) 1986-02-24
SK278327B6 (en) 1996-11-06
IE852054L (en) 1986-02-22
ES552050A0 (es) 1987-09-01
HU196754B (en) 1989-01-30
ES8707930A1 (es) 1987-09-01
KR870002073A (ko) 1987-03-28
DK378085A (da) 1986-02-23
LU88267I2 (es) 1994-02-03
NO167142B (no) 1991-07-01
JPS6479152A (en) 1989-03-24
CS403091A3 (en) 1992-06-17
HK52990A (en) 1990-07-20
ES8802497A1 (es) 1988-07-01
NL193065B (nl) 1998-05-06
PT81000A (en) 1985-09-01
KR920004482B1 (ko) 1992-06-05
GB2164336B (en) 1988-06-08
SE8503888L (sv) 1986-02-23
ES552051A0 (es) 1987-09-01
LU86047A1 (fr) 1986-02-28
JPH0550506B2 (es) 1993-07-29
AT394042B (de) 1992-01-27
NL193065C (nl) 1998-09-08
SA91120277B1 (ar) 2006-05-15
FI81568B (fi) 1990-07-31
GB2164336A (en) 1986-03-19
HUT40625A (en) 1987-01-28
IE58486B1 (en) 1993-09-22
NZ212895A (en) 1988-07-28
AU4657685A (en) 1986-02-27
NO853293L (no) 1986-02-24
DK378085D0 (da) 1985-08-20
ZW13185A1 (en) 1986-03-19
GR852016B (es) 1985-12-19
MX159974A (es) 1989-10-17
PT81000B (pt) 1988-03-03
ATA245485A (de) 1991-07-15
CY1494A (en) 1990-02-16
ES546324A0 (es) 1987-03-01
US4801599A (en) 1989-01-31
SG40889G (en) 1989-12-22
CH666684A5 (de) 1988-08-15
JPH0686430B2 (ja) 1994-11-02
NL980037I1 (nl) 1999-02-01
SE459920B (sv) 1989-08-21
FR2569402B1 (fr) 1989-09-22
NO1999007I1 (no) 1999-04-23
ES8707931A1 (es) 1987-09-01
PH22014A (en) 1988-05-02
NL8502296A (nl) 1986-03-17
NO167142C (no) 1991-10-09
FR2569402A1 (fr) 1986-02-28
ES552049A0 (es) 1988-07-01
ES552048A0 (es) 1987-09-01
GB8520924D0 (en) 1985-09-25
DK165949B (da) 1993-02-15
JPS6193162A (ja) 1986-05-12
DE3529997C2 (de) 1996-01-18
FI853206A0 (fi) 1985-08-21
NL980037I2 (nl) 1999-03-01
BG60409B2 (bg) 1995-02-28
US5011848A (en) 1991-04-30
AU578724B2 (en) 1988-11-03
SE8503888D0 (sv) 1985-08-20

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 20070611