JP2008521933A5 - - Google Patents

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Publication number
JP2008521933A5
JP2008521933A5 JP2007544570A JP2007544570A JP2008521933A5 JP 2008521933 A5 JP2008521933 A5 JP 2008521933A5 JP 2007544570 A JP2007544570 A JP 2007544570A JP 2007544570 A JP2007544570 A JP 2007544570A JP 2008521933 A5 JP2008521933 A5 JP 2008521933A5
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JP
Japan
Prior art keywords
compound
solution
salt
crystalline
seed crystal
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2007544570A
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English (en)
Japanese (ja)
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JP2008521933A (ja
JP4705956B2 (ja
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Application filed filed Critical
Priority claimed from PCT/US2005/043781 external-priority patent/WO2006060730A2/en
Publication of JP2008521933A publication Critical patent/JP2008521933A/ja
Publication of JP2008521933A5 publication Critical patent/JP2008521933A5/ja
Application granted granted Critical
Publication of JP4705956B2 publication Critical patent/JP4705956B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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JP2007544570A 2004-12-03 2005-12-02 Hivインテグラーゼ阻害剤のカリウム塩 Expired - Lifetime JP4705956B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US63313204P 2004-12-03 2004-12-03
US60/633,132 2004-12-03
PCT/US2005/043781 WO2006060730A2 (en) 2004-12-03 2005-12-02 Potassium salt of an hiv integrase inhibitor

Publications (3)

Publication Number Publication Date
JP2008521933A JP2008521933A (ja) 2008-06-26
JP2008521933A5 true JP2008521933A5 (enExample) 2010-12-24
JP4705956B2 JP4705956B2 (ja) 2011-06-22

Family

ID=36171569

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007544570A Expired - Lifetime JP4705956B2 (ja) 2004-12-03 2005-12-02 Hivインテグラーゼ阻害剤のカリウム塩

Country Status (35)

Country Link
US (2) US7754731B2 (enExample)
EP (2) EP1819700B1 (enExample)
JP (1) JP4705956B2 (enExample)
KR (2) KR20130122031A (enExample)
CN (1) CN101068793B (enExample)
AR (2) AR052034A1 (enExample)
AT (2) ATE534645T1 (enExample)
AU (1) AU2005311671B8 (enExample)
BR (1) BRPI0518760A8 (enExample)
CA (1) CA2588398C (enExample)
CR (1) CR9146A (enExample)
CY (1) CY1112859T1 (enExample)
DK (1) DK1819700T3 (enExample)
EA (1) EA012418B1 (enExample)
ES (2) ES2375788T3 (enExample)
GE (1) GEP20105086B (enExample)
HR (1) HRP20120066T1 (enExample)
IL (1) IL183614A (enExample)
MA (1) MA29120B1 (enExample)
ME (1) ME01985B (enExample)
MX (1) MX2007006639A (enExample)
MY (1) MY144320A (enExample)
NI (1) NI200700138A (enExample)
NO (1) NO338784B1 (enExample)
NZ (1) NZ555376A (enExample)
PE (1) PE20061148A1 (enExample)
PL (1) PL1819700T3 (enExample)
PT (1) PT1819700E (enExample)
RS (1) RS52197B (enExample)
SI (1) SI1819700T1 (enExample)
TN (1) TNSN07215A1 (enExample)
TW (1) TWI344463B (enExample)
UA (1) UA87884C2 (enExample)
WO (2) WO2006060730A2 (enExample)
ZA (1) ZA200704130B (enExample)

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EP3165220B2 (en) † 2004-12-03 2024-11-13 Merck Sharp & Dohme LLC Pharmaceutical composition containing an anti-nucleating agent
BRPI0518741A2 (pt) * 2004-12-03 2008-12-02 Merck & Co Inc uso de uma combinaÇço de uma droga diretamente metabolizada por ugt1a1 ou um seu sal farmaceuticamente aceitÁvel e atazanavir ou um seu sal farmaceuticamente aceitÁvel, e, combinaÇço farmacÊutica para administraÇço oral a um mamÍfero
CA2642504A1 (en) * 2006-03-14 2007-09-20 Brian K. Johnson Processes and apparatuses for the production of crystalline organic microparticle compositions by micro-milling and crystallization on micro-seed and their use
CA2657034A1 (en) 2006-07-19 2008-01-24 University Of Georgia Research Foundation, Inc. Pyridinone diketo acids: inhibitors of hiv replication in combination therapy
US7687509B2 (en) 2007-07-09 2010-03-30 Concert Pharmaceuticals Inc. Pyrimidinecarboxamide derivatives
EP2231621B1 (en) * 2008-01-08 2016-11-02 Merck Sharp & Dohme Corp. Process for preparing n-substituted hydroxypyrimidinone carboxamides
US8742105B2 (en) 2009-06-02 2014-06-03 Hetero Research Foundation Polymorphs of raltegravir potassium
WO2011024192A2 (en) 2009-07-27 2011-03-03 Matrix Laboratories Ltd Novel polymorphs of raltegravir
AU2010313571B2 (en) 2009-10-26 2014-07-31 Merck Sharp & Dohme Llc Solid pharmaceutical compositions containing an integrase inhibitor
DE102009056636A1 (de) 2009-12-02 2011-06-09 Ratiopharm Gmbh Raltegravir-Polymorphe
SG181524A1 (en) * 2009-12-07 2012-07-30 Univ Georgia Pyridinone hydroxycyclopentyl carboxamides: hiv integrase inhibitors with therapeutic applications
ES2362598B1 (es) * 2009-12-17 2012-06-13 Consejo Superior De Investigaciones Científicas (Csic) Uso del raltegravir y derivados para la elaboración de medicamentos destinados al tratamiento de infecciones por herpesvirus.
ES2524380T3 (es) * 2010-04-01 2014-12-05 Teva Pharmaceutical Industries Ltd. Sales de raltegravir y formas cristalinas de las mismas
WO2011120153A1 (en) * 2010-04-01 2011-10-06 Critical Outcome Technologies Inc. Compounds and method for treatment of hiv
WO2011148381A1 (en) * 2010-05-25 2011-12-01 Hetero Research Foundation Salts of raltegravir
US9107922B2 (en) 2010-07-16 2015-08-18 Concert Pharmaceuticals, Inc. Pyrimidinecarboxamide derivatives
CN101914067B (zh) * 2010-08-26 2012-07-11 陈岱岭 N-甲基嘧啶酮的合成方法
JO3209B1 (ar) * 2010-11-05 2018-03-08 H Lundbeck As طريقة لتصنيع نالتريكسون
WO2012103105A1 (en) 2011-01-24 2012-08-02 Assia Chemical Industries Ltd. Processes for preparing raltegravir and intermediates in the processes
WO2012106534A2 (en) * 2011-02-02 2012-08-09 The Regents Of The University Of California Hiv integrase inhibitors
US9163009B2 (en) 2011-04-06 2015-10-20 Lupin Limited Salts of raltegravir
EP2699094A4 (en) * 2011-04-22 2014-12-17 Merck Sharp & Dohme TASTE-MASKED FORMULATIONS BY RALTEGRAVIR
US9968607B2 (en) 2011-04-25 2018-05-15 Hetero Research Foundation Pharmaceutical compositions of raltegravir, methods of preparation and methods of use therof
EP2522665A1 (en) 2011-05-03 2012-11-14 Sandoz Ag Crystalline sodium salt of an HIV integrase inhibitor
ES2450944T3 (es) 2011-06-01 2014-03-25 Ratiopharm Gmbh Composición y comprimido que comprenden raltegravir
WO2013037731A1 (de) 2011-09-16 2013-03-21 Hexal Ag Neue polymorphe form von raltegravir-kalium
CN103130787B (zh) * 2011-11-24 2015-06-10 南开大学 嘧啶酮酰胺类化合物及其制备方法、抗hiv活性和抗tmv活性
CN103130788B (zh) * 2011-11-24 2015-09-02 南开大学 嘧啶酰胺类化合物及其制备方法、抗hiv活性和抗tmv活性
US9403809B2 (en) 2011-12-26 2016-08-02 Emcure Pharmaceuticals Limited Synthesis of raltegravir
KR20140114406A (ko) 2012-01-25 2014-09-26 루핀 리미티드 안정한 비정질 랄테그라빌 포타슘 프리믹스 및 이의 제조 방법
WO2014064711A2 (en) * 2012-10-22 2014-05-01 Hetero Research Foundation Methods of administering raltegravir and raltegravir compositions
EP2818470A1 (en) 2013-06-27 2014-12-31 Basf Se Cocrystals of raltegravir potassium
EP3022209B1 (en) 2013-07-17 2018-03-07 ratiopharm GmbH Dolutegravir potassium salt
PT3102565T (pt) 2014-02-03 2019-04-01 Mylan Laboratories Ltd Processos para a preparação de intermediários de raltegravir
WO2015140765A1 (en) * 2014-03-21 2015-09-24 Mylan Laboratories Ltd. A premix of crystalline raltegravir potassium salt and a process for the preparation thereof
US10257840B2 (en) 2014-10-22 2019-04-09 Telefonaktiebolaget Lm Ericsson (Publ) Operation of wireless local area network in the presence of periodic interference
US10259778B2 (en) 2014-11-10 2019-04-16 Aurobindo Pharma Ltd Process for the preparation of raltegravir
EP3472134B1 (en) 2016-06-21 2021-10-20 Pharmathen S.A. Process for preparing compounds useful as intermediates for the preparation of raltegravir
AU2017329049A1 (en) * 2016-09-15 2019-04-04 Lupin Limited Process for the preparation of pure and stable crystalline Raltegravir potassium Form 3
CN108610338A (zh) * 2016-12-12 2018-10-02 天津国际生物医药联合研究院 一种嘧啶酮酰胺类化合物的制备方法
CA3080012A1 (en) 2017-11-14 2019-05-23 Cambrex Profarmaco Milano S.R.L. Process for the preparation of raltegravir
US20210290548A1 (en) * 2018-06-06 2021-09-23 Merck Sharp & Dohme Corp. Formulations of raltegravir
GB201907305D0 (en) * 2019-05-23 2019-07-10 Douglas Pharmaceuticals Ltd Treatment of conditions
WO2021148992A1 (en) 2020-01-23 2021-07-29 Lupin Limited Pharmaceutical compositions of raltegravir

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BRPI0518741A2 (pt) 2004-12-03 2008-12-02 Merck & Co Inc uso de uma combinaÇço de uma droga diretamente metabolizada por ugt1a1 ou um seu sal farmaceuticamente aceitÁvel e atazanavir ou um seu sal farmaceuticamente aceitÁvel, e, combinaÇço farmacÊutica para administraÇço oral a um mamÍfero
RU2382648C2 (ru) 2004-12-03 2010-02-27 Мерк Энд Ко., Инк. Фармацевтический состав карбоксамидных ингибиторов интегразы вич, содержащий композицию с контролируемой скоростью высвобождения
EP3165220B2 (en) 2004-12-03 2024-11-13 Merck Sharp & Dohme LLC Pharmaceutical composition containing an anti-nucleating agent

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