发明名称 SYNTHESIS AND PURIFICATION OF VALACYCLOVIR
摘要 The present invention relates to protected valacyclovir, N-tert- butoxycarbonyl-L-valine 2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl) methoxy] ethyl ester, and a method of making it. The present invention further relates to a method of making valacyclovir including the steps of coupling an amine protected valine selected from N-tbutoxycarbonyl valine and N-formyl valine with acyclovir using a coupling agent to form a protected valacyclovir, and deprotecting the protected valacyclovir to form valacyclovir or a pharmaceutically acceptable salt thereof. The present invention further relates to valacyclovir in pure form, a method of making pure valacyclovir, and to compositions containing pure valacyclovir. ® KIPO & WIPO 2007
申请公布号 KR20070020149(A) 申请公布日期 2007.02.16
申请号 KR20077002062 申请日期 2007.01.26
申请人 TEVA PHARMACEUTICAL INDUSTRIES LTD. 发明人 ETINGER MARINA YU;YUDOVICH LEV M.;YUZEFOVICH MICHAEL;NISNEVICH GENNADY A.;DOLITZKI BEN ZION;PERTSIKOV BORIS;TISHIN BORIS;BLASBERGER DINA
分类号 C07D473/18;A61K;A61K31/522;A61P31/22;C07B51/00;C07D473/00 主分类号 C07D473/18
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