AR049995A1 - Un procedimiento de preparacion de derivados n-piperidino-1,5-difenilpirazol-3-carboxamida - Google Patents

Un procedimiento de preparacion de derivados n-piperidino-1,5-difenilpirazol-3-carboxamida

Info

Publication number
AR049995A1
AR049995A1 ARP050102971A ARP050102971A AR049995A1 AR 049995 A1 AR049995 A1 AR 049995A1 AR P050102971 A ARP050102971 A AR P050102971A AR P050102971 A ARP050102971 A AR P050102971A AR 049995 A1 AR049995 A1 AR 049995A1
Authority
AR
Argentina
Prior art keywords
formula
group
halogen atom
alkyl
difenilpirazol
Prior art date
Application number
ARP050102971A
Other languages
English (en)
Inventor
Marc Daumas
Alain Dlubala
Philippe Vayron
Raphael Sole
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 AR049995A1 publication Critical patent/AR049995A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34Tobacco-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Addiction (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Child & Adolescent Psychology (AREA)
  • Psychiatry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Reivindicacion 1: Procedimiento de preparacion de un compuesto de formula (1), donde: R1 representa un átomo de hidrogeno o de halogeno o un grupo C1-4 alquilo; R2, R3, R4, R5, R6, R7 representan cada uno, independientemente uno del otro, un átomo de hidrogeno o de halogeno o un grupo C1-4 alquilo, C1-4 alcoxi, trifluorometilo; y de sus sales, caracterizado porque: se hace reaccionar un derivado de pentano de formula: X-(CH2)5-X', donde X y X' representan, cada una independientemente, un átomo de halogeno o un grupo YSO2O- donde Y representa un grupo C1-4 alquilo, C1-4 perfluoroalquilo, fenilo no sustituido o sustituido por un grupo metilo, cloro o nitro, sobre un derivado de pirazol-3-carbohidrazida de formula (2), donde R1, R2, R3, R4, R5 R6, R7 son tales como se definieran anteriormente para la formula (1) en presencia de una base, en un solvente y a una temperatura comprendida entre la temperatura ambiente y la temperatura de reflujo del solvente.
ARP050102971A 2004-07-22 2005-07-19 Un procedimiento de preparacion de derivados n-piperidino-1,5-difenilpirazol-3-carboxamida AR049995A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0408111A FR2873372B1 (fr) 2004-07-22 2004-07-22 Procede de preparation de derives n-piperidino-1,5- diphenylpyrazole-3-carboxamide

Publications (1)

Publication Number Publication Date
AR049995A1 true AR049995A1 (es) 2006-09-20

Family

ID=34949586

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050102971A AR049995A1 (es) 2004-07-22 2005-07-19 Un procedimiento de preparacion de derivados n-piperidino-1,5-difenilpirazol-3-carboxamida

Country Status (21)

Country Link
US (1) US7462632B2 (es)
EP (1) EP1773783B1 (es)
JP (1) JP4879175B2 (es)
KR (1) KR20070036050A (es)
CN (1) CN100537543C (es)
AR (1) AR049995A1 (es)
AT (1) ATE466843T1 (es)
AU (1) AU2005276350A1 (es)
BR (1) BRPI0510399A (es)
CA (1) CA2564223A1 (es)
DE (1) DE602005021110D1 (es)
FR (1) FR2873372B1 (es)
IL (1) IL179107A0 (es)
MA (1) MA28576B1 (es)
MX (1) MXPA06012954A (es)
NO (1) NO20071008L (es)
RU (1) RU2329252C1 (es)
TW (1) TW200609223A (es)
UY (1) UY29023A1 (es)
WO (1) WO2006021652A1 (es)
ZA (1) ZA200609639B (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1816125A1 (en) * 2006-02-02 2007-08-08 Ranbaxy Laboratories, Ltd. Novel crystalline forms of an antagonist of CB1 cannabinoid receptor and preparation method thereof
US20100076022A1 (en) * 2006-09-01 2010-03-25 Hetero Drugs Limited Novel polymorphs of rimonabant
EP2061783A2 (en) * 2006-09-11 2009-05-27 Hetero Drugs Limited Improved process for rimonabant
WO2008035023A1 (en) * 2006-09-19 2008-03-27 Cipla Limited Polymorphs of rimonabant
EP1944297A1 (en) * 2007-01-09 2008-07-16 Miklós Vértessy Solid and crystalline rimonabant and processes for preparation, and pharmaceutical composition thereof
EP1947090A1 (en) * 2007-01-17 2008-07-23 Laboratorios del Dr. Esteve S.A. Method for preparing N-piperidino-1,5-diphenylpyrazole-3-carboxamide and derivatives
WO2008088900A2 (en) * 2007-01-18 2008-07-24 Teva Pharmaceutical Industries Ltd. Polymorphic forms of rimonabant base and processes for preparation thereof
WO2008102367A1 (en) * 2007-02-19 2008-08-28 Darmesh Mahendrabhai Shah Process for preparation of pyrazole derivatives
FR2913018A1 (fr) * 2007-02-23 2008-08-29 Sanofi Aventis Sa Solution solide amorphe contenant un derive de pyrazole-3-carboxamide sous forme amorphe et des excipients stabilisateurs
WO2009109222A1 (en) * 2008-03-04 2009-09-11 Maprimed, S. A. Process for the preparation of rimonabant
WO2010079241A1 (es) 2009-01-12 2010-07-15 Fundacion Hospital Nacional De Paraplejicos Para La Investigacion Y La Integracion Uso de antagonistas y/o agonistas inversos de los receptores cb1 para la preparación de medicamentos que incrementen la excitabilidad de las motoneuronas

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2713225B1 (fr) * 1993-12-02 1996-03-01 Sanofi Sa N-pipéridino-3-pyrazolecarboxamide substitué.
FR2714057B1 (fr) * 1993-12-17 1996-03-08 Sanofi Elf Nouveaux dérivés du 3-pyrazolecarboxamide, procédé pour leur préparation et compositions pharmaceutiques les contenant.
JP4314339B2 (ja) * 2002-08-22 2009-08-12 三井化学アグロ株式会社 ニコチンアミドラゾン誘導体

Also Published As

Publication number Publication date
WO2006021652A1 (fr) 2006-03-02
MXPA06012954A (es) 2007-02-12
BRPI0510399A (pt) 2007-11-13
ZA200609639B (en) 2008-08-27
UY29023A1 (es) 2006-02-24
AU2005276350A1 (en) 2006-03-02
JP4879175B2 (ja) 2012-02-22
FR2873372A1 (fr) 2006-01-27
JP2008506756A (ja) 2008-03-06
CN1956963A (zh) 2007-05-02
EP1773783B1 (fr) 2010-05-05
CN100537543C (zh) 2009-09-09
DE602005021110D1 (de) 2010-06-17
NO20071008L (no) 2007-02-21
US20080119653A1 (en) 2008-05-22
MA28576B1 (fr) 2007-05-02
KR20070036050A (ko) 2007-04-02
ATE466843T1 (de) 2010-05-15
US7462632B2 (en) 2008-12-09
RU2329252C1 (ru) 2008-07-20
TW200609223A (en) 2006-03-16
FR2873372B1 (fr) 2006-09-08
EP1773783A1 (fr) 2007-04-18
CA2564223A1 (fr) 2006-03-02
IL179107A0 (en) 2007-03-08

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