PE20050585A1 - Sal y forma cristalina de la misma de un antagonista del receptor del factor de liberacion de corticotropina - Google Patents

Sal y forma cristalina de la misma de un antagonista del receptor del factor de liberacion de corticotropina

Info

Publication number
PE20050585A1
PE20050585A1 PE2004001149A PE2004001149A PE20050585A1 PE 20050585 A1 PE20050585 A1 PE 20050585A1 PE 2004001149 A PE2004001149 A PE 2004001149A PE 2004001149 A PE2004001149 A PE 2004001149A PE 20050585 A1 PE20050585 A1 PE 20050585A1
Authority
PE
Peru
Prior art keywords
compound
salt
release factor
antagonist
receptor
Prior art date
Application number
PE2004001149A
Other languages
English (en)
Inventor
Paul J Gilligan
Shelley Rabel
Paul A Meenan
Original Assignee
Bristol Myers Squibb Pharma Co
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 Bristol Myers Squibb Pharma Co filed Critical Bristol Myers Squibb Pharma Co
Publication of PE20050585A1 publication Critical patent/PE20050585A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—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
    • A61P25/22—Anxiolytics
    • 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
    • A61P25/24—Antidepressants
    • 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
    • A61P3/04—Anorexiants; Antiobesity agents

Landscapes

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

Abstract

SE REFIERE A UN COMPUESTO QUE ES UNA SAL BENCENOSULFONATO DE 4-(BIS(2-METOXIETIL)AMINO)-2,7-DIMETIL-8-(2-METIL-4-METOXIFENIL)-[1,5-O]-PIRAZOLO-1,3,5-TRIAZINA. DONDE n ES DE 0 A 1. EL COMPUESTO TIENE UN TERMOGRAMA CALORIMETRICO DE EXPLORACION DIFERENCIAL CON UN MAXIMO DE 94 °C. EL COMPUESTO ES CRISTALINO Y TIENE UN ESPECTRO DE DIFRACCION DE RAYOS X EN POLVO Y PRESENTA PICOS QUE COMPRENDEN CUATRO O MAS VALORES 2-THETA CATALOGADOS EN UNA TABLA CUYOS VALORES SON: 6,7 +/- 0,2; 8,0 +/- 0,2; 10,4 +/- 0,2; 11,7 +/- 0,2; 12,3 +/- 0,2; 14,6 +/- 0,2 ENTRE OTROS VALORES. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE EL COMPUESTO CITADO Y UN VEHICULO FARMACEUTICAMENTE ACEPTABLE UTIL PARA TRATAMIENTOS DE TRASTORNOS RELACIONADOS CON EL FACTOR DE LIBERACION DE CORTICOTROPINA (CRF)
PE2004001149A 2003-11-25 2004-11-24 Sal y forma cristalina de la misma de un antagonista del receptor del factor de liberacion de corticotropina PE20050585A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US52491703P 2003-11-25 2003-11-25
US10/985,115 US7153961B2 (en) 2003-11-25 2004-11-10 Salt and crystalline form thereof of a corticotropin releasing factor receptor antagonist

Publications (1)

Publication Number Publication Date
PE20050585A1 true PE20050585A1 (es) 2005-09-05

Family

ID=34595203

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2004001149A PE20050585A1 (es) 2003-11-25 2004-11-24 Sal y forma cristalina de la misma de un antagonista del receptor del factor de liberacion de corticotropina

Country Status (4)

Country Link
US (1) US7153961B2 (es)
PE (1) PE20050585A1 (es)
TW (1) TW200530239A (es)
WO (1) WO2005051394A1 (es)

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3910907A (en) * 1973-07-09 1975-10-07 Icn Pharmaceuticals Pyrazolo(1,5-a)-1,3,5-triazines
US4824834A (en) * 1986-10-31 1989-04-25 Otsuka Pharmaceutical Company, Limited Pyrazolotriazine compounds
DE3722072A1 (de) * 1987-07-01 1989-01-12 Schering Ag 6,7-dihydro-pyrazolo(1,5-a)(1,3,5) triazin-2-sulfonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als mittel mit herbizider und pflanzenwuchsregulierender wirkung
JP2691317B2 (ja) * 1989-08-25 1997-12-17 株式会社大塚製薬工場 ４―ヒドロキシ―８―（３―低級アルコキシ―４―フェニルスルフィニルフェニル）ピラゾロ〔１，５―ａ〕―１，３，５―トリアジン光学活性体の塩類及びその製造方法
US5484760A (en) * 1990-12-31 1996-01-16 Monsanto Company Herbicide antidotes as safeners for reducing phytotoxicity resulting from synergistic interaction between herbicides and other pesticides
AU667575B2 (en) 1992-10-20 1996-03-28 Otsuka Pharmaceutical Co., Ltd. Condensed pyrazole derivatives, method of manufacturing the same, and androgen inhibitor
CN1088574A (zh) 1992-12-24 1994-06-29 中国科学院化学研究所 2,6-二甲基-4-叔丁基-3-硝基-苯乙氰的合成方法
US6060478A (en) * 1996-07-24 2000-05-09 Dupont Pharmaceuticals Azolo triazines and pyrimidines
US6313124B1 (en) * 1997-07-23 2001-11-06 Dupont Pharmaceuticals Company Tetrazine bicyclic compounds
US6124289A (en) 1996-07-24 2000-09-26 Dupont Pharmaceuticals Co. Azolo triazines and pyrimidines
US6191131B1 (en) * 1997-07-23 2001-02-20 Dupont Pharmaceuticals Company Azolo triazines and pyrimidines
DK0915880T3 (da) 1996-07-24 2008-02-11 Bristol Myers Squibb Pharma Co Azolotriaziner og pyrimidiner
KR20000035934A (ko) 1996-08-28 2000-06-26 디. 제이. 우드, 스피겔 알렌 제이 치환된 6,5-헤테로-비사이클릭 유도체
US6139809A (en) * 1998-04-09 2000-10-31 Rodden; Raymond M. Injected flow ozone generator
JP2003510326A (ja) 1999-09-30 2003-03-18 ニューロジェン・コーポレーション アミノ置換ピラゾロ［１，５−ａ］−１，５−ピリミジン類及びピラゾロ［１，５−ａ］−１，３，５−トリアジン類
JP2001302658A (ja) 2000-04-18 2001-10-31 Showa Denko Kk ３−イソクロマノン類の製造方法
HU229317B1 (en) 2001-03-13 2013-10-28 Bristol Myers Squibb Pharma Co 4-(2-butylamino)-2,7-dimethyl-8-(2-methyl-6-methoxypyrid-3-yl) pyrazolo-[1,5-a]-1,3,5-triazine derivatives, and enantiomers of the same az cortikotropine releasing factor (cfr) ligands

Also Published As

Publication number Publication date
US20050113375A1 (en) 2005-05-26
WO2005051394A1 (en) 2005-06-09
TW200530239A (en) 2005-09-16
US7153961B2 (en) 2006-12-26

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