BRPI0514431A - processo para a sìntese de indóis n-alquilados c-2, c-3 substituìdos úteis como inibidores da cpla2 - Google Patents

processo para a sìntese de indóis n-alquilados c-2, c-3 substituìdos úteis como inibidores da cpla2

Info

Publication number
BRPI0514431A
BRPI0514431A BRPI0514431-0A BRPI0514431A BRPI0514431A BR PI0514431 A BRPI0514431 A BR PI0514431A BR PI0514431 A BRPI0514431 A BR PI0514431A BR PI0514431 A BRPI0514431 A BR PI0514431A
Authority
BR
Brazil
Prior art keywords
synthesis
substituted
formula
compound
cpla2 inhibitors
Prior art date
Application number
BRPI0514431-0A
Other languages
English (en)
Inventor
Ronald S Michalak
Mahmut Levent
Frederick J Vyverberg
Ara R Boyajian
Panolil Raveendranath
Michel Cantin
Alan Stockton
Michael W Winkley
Mousumi Ghosh
Christoph Dehnhardt
Charles Guinosso
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of BRPI0514431A publication Critical patent/BRPI0514431A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/14—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/38—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reaction of ammonia or amines with sulfonic acids, or with esters, anhydrides, or halides thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
    • C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PROCESSO PARA A SìNTESE DE INDóIS N-ALQUILADOS C-2, C3 SUBSTITUìDOS úTEIS COMO INIBIDORES DA CPLA~ 2~ A presente invenção fornece um método para fazer um composto de fórmula 1: compreendendo as etapas de reagir os compostos de fórmulas 2 e 3: para produzir um composto de fórmula 4: em que R¬ ¹¬,R¬ ²¬, R¬ ³¬, R¬ 4¬ e R¬ 5¬ são definidos conforme aqui descrito. O composto de fórmula 4 é, a seguir, convertido para o composto de fórmula 1. A invenção compreende ainda compostos de fórmulas 3 e 4 e métodos para fazer compostos de fórmulas 3 e 4.
BRPI0514431-0A 2004-08-19 2005-08-18 processo para a sìntese de indóis n-alquilados c-2, c-3 substituìdos úteis como inibidores da cpla2 BRPI0514431A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US60312404P 2004-08-19 2004-08-19
PCT/US2005/029338 WO2006023611A1 (en) 2004-08-19 2005-08-18 Process for the synthesis c-2, c-3 substituted n-alkylated indoles useful as cpla2 inhibitors

Publications (1)

Publication Number Publication Date
BRPI0514431A true BRPI0514431A (pt) 2008-06-10

Family

ID=35219553

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0514431-0A BRPI0514431A (pt) 2004-08-19 2005-08-18 processo para a sìntese de indóis n-alquilados c-2, c-3 substituìdos úteis como inibidores da cpla2

Country Status (24)

Country Link
US (3) US7582772B2 (pt)
EP (1) EP1778629B1 (pt)
JP (1) JP2008510707A (pt)
KR (1) KR20070043036A (pt)
CN (2) CN101006048B (pt)
AR (1) AR053410A1 (pt)
AT (1) ATE517084T1 (pt)
AU (1) AU2005277392A1 (pt)
BR (1) BRPI0514431A (pt)
CA (1) CA2576008A1 (pt)
CR (1) CR8936A (pt)
EC (1) ECSP077244A (pt)
GT (1) GT200500224A (pt)
HN (1) HN2005000474A (pt)
IL (1) IL181364A0 (pt)
MX (1) MX2007002042A (pt)
NO (1) NO20071253L (pt)
PE (1) PE20060628A1 (pt)
RU (1) RU2401829C2 (pt)
SG (1) SG155214A1 (pt)
SV (1) SV2006002200A (pt)
TW (1) TW200609214A (pt)
UA (1) UA85428C2 (pt)
WO (1) WO2006023611A1 (pt)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7605156B2 (en) 2001-12-03 2009-10-20 Wyeth Methods for the use of inhibitors of cytosolic phospholipase A2
US7713964B2 (en) * 2001-12-03 2010-05-11 Wyeth Llc Methods for treating asthmatic conditions
US7342119B2 (en) * 2003-09-30 2008-03-11 Wyeth Holdings Corporation Process for the synthesis of a CPLA2 inhibitor
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
GT200600228A (es) * 2005-05-27 2006-12-26 Inhibidores de la fosfolipasa a2 citosolica
BRPI0718042A2 (pt) * 2006-10-31 2013-11-12 Wyeth Corp Formulações semissólidas de inibidores de enzima fosfolipase
EP2104498A2 (en) * 2006-10-31 2009-09-30 Wyeth Liquid formulations of phospholipase enzyme inhibitors

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02115157A (ja) * 1988-10-24 1990-04-27 Hokko Chem Ind Co Ltd スルホニルグリシン誘導体および除草剤
ATE440824T1 (de) * 1999-12-09 2009-09-15 Bayer Cropscience Ag Nitro-sulfobenzamide
US7101875B2 (en) * 2001-12-03 2006-09-05 Wyeth Methods for treating arthritic disorders
US7713964B2 (en) * 2001-12-03 2010-05-11 Wyeth Llc Methods for treating asthmatic conditions
US6797708B2 (en) * 2001-12-03 2004-09-28 Wyeth Inhibitors of cytosolic phospholipase A2
US7605156B2 (en) 2001-12-03 2009-10-20 Wyeth Methods for the use of inhibitors of cytosolic phospholipase A2
US6984735B2 (en) * 2001-12-03 2006-01-10 Wyeth Process for making an aldehyde
JP4657605B2 (ja) * 2001-12-03 2011-03-23 ワイス・エルエルシー 細胞質内ホスホリパーゼａ２の阻害剤
US6635771B2 (en) * 2001-12-03 2003-10-21 Wyeth N-benzhydryl indole compounds
TW200510305A (en) * 2003-07-25 2005-03-16 Wyeth Corp Process for the preparation of CPLA2 inhibitors
WO2005012235A1 (en) 2003-07-29 2005-02-10 Ciba Specialty Chemicals Holding Inc. 3-aryl-2-cyano-3-hydroxy-acrylic acid derivatives
US7582771B2 (en) * 2003-09-03 2009-09-01 Wyeth Process for the synthesis of cPLA2 inhibitors
US7342119B2 (en) * 2003-09-30 2008-03-11 Wyeth Holdings Corporation Process for the synthesis of a CPLA2 inhibitor
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

Also Published As

Publication number Publication date
IL181364A0 (en) 2007-07-04
HN2005000474A (es) 2009-04-07
RU2007105231A (ru) 2008-09-27
US20090306428A1 (en) 2009-12-10
CN101006048A (zh) 2007-07-25
SV2006002200A (es) 2006-05-09
PE20060628A1 (es) 2006-08-14
NO20071253L (no) 2007-05-15
WO2006023611A1 (en) 2006-03-02
US8034960B2 (en) 2011-10-11
TW200609214A (en) 2006-03-16
CN101006048B (zh) 2011-07-06
MX2007002042A (es) 2007-03-29
ECSP077244A (es) 2007-03-29
CA2576008A1 (en) 2006-03-02
RU2401829C2 (ru) 2010-10-20
EP1778629B1 (en) 2011-07-20
KR20070043036A (ko) 2007-04-24
CN101830837A (zh) 2010-09-15
JP2008510707A (ja) 2008-04-10
AU2005277392A1 (en) 2006-03-02
US20060041005A1 (en) 2006-02-23
SG155214A1 (en) 2009-09-30
GT200500224A (es) 2006-03-21
US7582772B2 (en) 2009-09-01
CR8936A (es) 2007-04-26
AR053410A1 (es) 2007-05-09
ATE517084T1 (de) 2011-08-15
EP1778629A1 (en) 2007-05-02
UA85428C2 (ru) 2009-01-26
US7842837B2 (en) 2010-11-30
US20110054189A1 (en) 2011-03-03

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Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 8A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2260 DE 29/04/2014.