CL2008000598A1 - Procedimiento de preparacion de 3-metil-4-fenilisoxazolo [3,4-d]piridazin-7(6h)-ona. - Google Patents

Procedimiento de preparacion de 3-metil-4-fenilisoxazolo [3,4-d]piridazin-7(6h)-ona.

Info

Publication number
CL2008000598A1
CL2008000598A1 CL200800598A CL2008000598A CL2008000598A1 CL 2008000598 A1 CL2008000598 A1 CL 2008000598A1 CL 200800598 A CL200800598 A CL 200800598A CL 2008000598 A CL2008000598 A CL 2008000598A CL 2008000598 A1 CL2008000598 A1 CL 2008000598A1
Authority
CL
Chile
Prior art keywords
piridazin
phenylisoxazolo
ona
methyl
preparation procedure
Prior art date
Application number
CL200800598A
Other languages
English (en)
Inventor
Marchueta Hereu Xavier Iolanda
Original Assignee
Almirall Lab
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 Almirall Lab filed Critical Almirall Lab
Publication of CL2008000598A1 publication Critical patent/CL2008000598A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
CL200800598A 2007-03-02 2008-02-27 Procedimiento de preparacion de 3-metil-4-fenilisoxazolo [3,4-d]piridazin-7(6h)-ona. CL2008000598A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES200700564A ES2320954B1 (es) 2007-03-02 2007-03-02 Nuevo procedimiento de preparacion de 3-metil-4-fenilisoxazolo (3,4-d)iridazin-7(6h)-ona.

Publications (1)

Publication Number Publication Date
CL2008000598A1 true CL2008000598A1 (es) 2008-09-05

Family

ID=38617235

Family Applications (1)

Application Number Title Priority Date Filing Date
CL200800598A CL2008000598A1 (es) 2007-03-02 2008-02-27 Procedimiento de preparacion de 3-metil-4-fenilisoxazolo [3,4-d]piridazin-7(6h)-ona.

Country Status (23)

Country Link
US (1) US20100137591A1 (es)
EP (1) EP2125830B1 (es)
JP (1) JP2010520158A (es)
KR (1) KR20090116753A (es)
CN (1) CN101679453A (es)
AR (1) AR065511A1 (es)
AT (1) ATE496923T1 (es)
AU (1) AU2008224206A1 (es)
BR (1) BRPI0807273A2 (es)
CA (1) CA2679619A1 (es)
CL (1) CL2008000598A1 (es)
DE (1) DE602008004742D1 (es)
EC (1) ECSP099558A (es)
ES (1) ES2320954B1 (es)
IL (1) IL200166A0 (es)
MX (1) MX2009009232A (es)
NZ (1) NZ578671A (es)
PE (1) PE20081793A1 (es)
RU (1) RU2009136314A (es)
TW (1) TW200844105A (es)
UY (1) UY30913A1 (es)
WO (1) WO2008107064A1 (es)
ZA (1) ZA200905193B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2211344B1 (es) * 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251866B1 (es) 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) * 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5679696A (en) * 1992-07-28 1997-10-21 Rhone-Poulenc Rorer Limited Compounds containing phenyl linked to aryl or heteroaryl by an aliphatic-or heteroatom-containing linking group
DE19533975A1 (de) * 1995-09-14 1997-03-20 Merck Patent Gmbh Arylalkyl-diazinone
DE19540475A1 (de) * 1995-10-20 1997-04-24 Schering Ag Chirale Methylphenyloxazolidinone
WO1997044036A1 (en) * 1996-05-20 1997-11-27 Darwin Discovery Limited Quinoline carboxamides as tnf inhibitors and as pde-iv inhibitors
CZ371998A3 (cs) * 1996-05-20 1999-03-17 Darwin Discovery Limited Benzofuranové karboxamidy a jejich terapeutické použití
DK1045690T3 (da) * 1997-11-25 2003-08-04 Warner Lambert Co Benzensulfonamidinhibitorer af PDE-IV og deres terapeutiske anvendelse
EP1157007A1 (en) * 1999-02-25 2001-11-28 Merck Frosst Canada Inc. Pde iv inhibiting compounds, compositions and methods of treatment
US6699890B2 (en) * 2000-12-22 2004-03-02 Memory Pharmaceuticals Corp. Phosphodiesterase 4 inhibitors
KR100951218B1 (ko) * 2001-10-16 2010-04-05 메모리 파마슈티칼스 코포레이션 신경계 증후군의 치료를 위한 ｐｄｅ-4 억제제로서의4-(4-알콕시-3-히드록시페닐)-2-피롤리돈 유도체
MY130622A (en) * 2001-11-05 2007-07-31 Novartis Ag Naphthyridine derivatives, their preparation and their use as phosphodiesterase isoenzyme 4 (pde4) inhibitors
ES2195785B1 (es) * 2002-05-16 2005-03-16 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
CA2506297A1 (en) * 2002-11-19 2004-06-03 Memory Pharmaceuticals Corporation Pyridine n-oxide compounds as phosphodiesterase 4 inhibitors
ES2211344B1 (es) * 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
AU2004232973A1 (en) * 2003-04-18 2004-11-04 Memory Pharmaceuticals Corporation Pyrazole derivatives as phosphodiesterase 4 inhibitors
ES2232306B1 (es) * 2003-11-10 2006-08-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251866B1 (es) * 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) * 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
JP2011504505A (ja) * 2007-11-21 2011-02-10 デコード ジェネティクス イーエイチエフ 肺および心血管障害を治療するためのビアリールｐｄｅ４抑制剤

Also Published As

Publication number Publication date
AR065511A1 (es) 2009-06-10
ECSP099558A (es) 2009-09-29
WO2008107064A1 (en) 2008-09-12
ES2320954B1 (es) 2010-03-16
EP2125830A1 (en) 2009-12-02
BRPI0807273A2 (pt) 2014-04-29
JP2010520158A (ja) 2010-06-10
UY30913A1 (es) 2008-07-31
ZA200905193B (en) 2010-05-26
KR20090116753A (ko) 2009-11-11
EP2125830B1 (en) 2011-01-26
ES2320954A1 (es) 2009-05-29
MX2009009232A (es) 2009-10-12
RU2009136314A (ru) 2011-04-10
CA2679619A1 (en) 2008-09-12
ATE496923T1 (de) 2011-02-15
NZ578671A (en) 2011-04-29
CN101679453A (zh) 2010-03-24
IL200166A0 (en) 2010-04-15
TW200844105A (en) 2008-11-16
DE602008004742D1 (de) 2011-03-10
US20100137591A1 (en) 2010-06-03
AU2008224206A1 (en) 2008-09-12
PE20081793A1 (es) 2008-12-18

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