KR20100138959A - N-[[4-플루오로-2-(5-메틸-1H-1,2,4-트리아졸-1-일)페닐]메틸]-4,6,7,9-테트라히드로-3-히드록시-9,9-디메틸-4-옥소-피리미도[2,1-c][1,4]옥사진-2-카르복스아미드, 나트륨 염 일수화물의 결정질 형태 - Google Patents

N-[[4-플루오로-2-(5-메틸-1H-1,2,4-트리아졸-1-일)페닐]메틸]-4,6,7,9-테트라히드로-3-히드록시-9,9-디메틸-4-옥소-피리미도[2,1-c][1,4]옥사진-2-카르복스아미드, 나트륨 염 일수화물의 결정질 형태 Download PDF

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Publication number
KR20100138959A
KR20100138959A KR1020107021250A KR20107021250A KR20100138959A KR 20100138959 A KR20100138959 A KR 20100138959A KR 1020107021250 A KR1020107021250 A KR 1020107021250A KR 20107021250 A KR20107021250 A KR 20107021250A KR 20100138959 A KR20100138959 A KR 20100138959A
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South Korea
Prior art keywords
hiv
inhibitor
crystalline form
compound
methyl
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KR1020107021250A
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English (en)
Korean (ko)
Inventor
캔디스 와이. 최
얼리셔 티 ?R이 응
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브리스톨-마이어스 스큅 컴퍼니
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Publication of KR20100138959A publication Critical patent/KR20100138959A/ko
Withdrawn legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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
    • C07D498/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • AIDS & HIV (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
KR1020107021250A 2008-03-27 2009-03-26 N-[[4-플루오로-2-(5-메틸-1H-1,2,4-트리아졸-1-일)페닐]메틸]-4,6,7,9-테트라히드로-3-히드록시-9,9-디메틸-4-옥소-피리미도[2,1-c][1,4]옥사진-2-카르복스아미드, 나트륨 염 일수화물의 결정질 형태 Withdrawn KR20100138959A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US3998908P 2008-03-27 2008-03-27
US61/039,989 2008-03-27

Publications (1)

Publication Number Publication Date
KR20100138959A true KR20100138959A (ko) 2010-12-31

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ID=41008867

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020107021250A Withdrawn KR20100138959A (ko) 2008-03-27 2009-03-26 N-[[4-플루오로-2-(5-메틸-1H-1,2,4-트리아졸-1-일)페닐]메틸]-4,6,7,9-테트라히드로-3-히드록시-9,9-디메틸-4-옥소-피리미도[2,1-c][1,4]옥사진-2-카르복스아미드, 나트륨 염 일수화물의 결정질 형태

Country Status (8)

Country Link
US (1) US7968541B2 (enExample)
EP (1) EP2280980B1 (enExample)
JP (1) JP2011515491A (enExample)
KR (1) KR20100138959A (enExample)
CN (1) CN102046637B (enExample)
AU (1) AU2009228254A1 (enExample)
MX (1) MX2010010244A (enExample)
WO (1) WO2009120841A1 (enExample)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106478661A (zh) * 2015-08-25 2017-03-08 华北制药集团新药研究开发有限责任公司 苯并恶唑并恶嗪酮类化合物wa1-089的晶型e及其制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK9742002A3 (en) * 2000-01-07 2003-02-04 Transform Pharmaceuticals Inc High-throughput formation, identification, and analysis of diverse solid-forms
US7157447B2 (en) * 2004-05-28 2007-01-02 Bristol-Myers Squibb Company Bicyclic heterocycles as HIV integrase inhibitors
US7176196B2 (en) * 2004-05-28 2007-02-13 Bristol-Myers Squibb Company Bicyclic heterocycles as HIV integrase inhibitors
WO2007064316A1 (en) * 2005-11-30 2007-06-07 Bristol-Myers Squibb Company Bicyclic heterocycles as hiv integrase inhibitors
WO2007064502A1 (en) * 2005-12-01 2007-06-07 Bristol-Myers Squibb Company Forms of n-[(4-fluorophenyl)methyl]-4,6,7,9-tetrahydro-3-hydroxy-9,9-dimethyl-4-oxo-pyrimido[2,1-c][1,4]oxazine-2-carboxamide
US7897593B2 (en) * 2006-05-30 2011-03-01 Bristol-Myers Squibb Company HIV integrase inhibitors

Also Published As

Publication number Publication date
WO2009120841A1 (en) 2009-10-01
EP2280980A1 (en) 2011-02-09
MX2010010244A (es) 2010-10-05
JP2011515491A (ja) 2011-05-19
AU2009228254A1 (en) 2009-10-01
US7968541B2 (en) 2011-06-28
US20090253692A1 (en) 2009-10-08
CN102046637B (zh) 2013-10-02
CN102046637A (zh) 2011-05-04
EP2280980B1 (en) 2016-03-23

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PA0105 International application

Patent event date: 20100924

Patent event code: PA01051R01D

Comment text: International Patent Application

PG1501 Laying open of application
PC1203 Withdrawal of no request for examination
WITN Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid