发明名称 METHODS FOR ISOLATING PROPARGYLATED AMINOINDANS
摘要 Disclosed is a process for isolating from a reaction mixture a salt of a mono-propargylated aminoindan having the structure (I) wherein R1 is H, hydroxyl, alkoxy or (II) wherein Y is 0 or S; R2 and R3 is each independently, C1-8 alkyl, C6-12 aryl, C6-12 aralkyl, each optionally halo substituted, or hydrogen ; where the reaction mixture further comprises a solven, a primary aminoindan having the structure (III) wherein R1 is defined as above, and a tertiary aminoindan having the structure (IV) the process comprising d) adding an acid to the reaction mixture; e) crystallizing the mono-propargylated aminoindan under conditions suitable for the formation of a crystalline salt of the mono-propargylated aminoindan ; and f) recovering the crystalline salt of the mono- propargylated aminoindan, wherein the process is performed without addition of an organic solvent. Also disclosed are the crystalline diastereomeric salts produced by the process and pharmaceutical compositions containing the salts.
申请公布号 WO2007061717(A3) 申请公布日期 2009.04.30
申请号 WO2006US44327 申请日期 2006.11.15
申请人 TEVA PHARMACEUTICAL INDUSTRIES, LTD.;TEVA PHARMACEUTICALS USA, INC. 发明人 FRENKEL, ANTON;LIDOR-HADAS, RAMY;GUREVICH, EDUARD;ATTILI, GSAN
分类号 C07C211/42;A61K31/13;C07C209/84;C07C209/86;C07C209/88 主分类号 C07C211/42
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