Process for making hiv protease inhibitors

A process for making a clinically efficacious HIV protease inhibitor Compound J eliminates one step in its synthesis, by an improved, alternative synthesis of the 2(S)-4-picolyl-2-piperazine-t-butyl-carboxamide intermediate.

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Bibliographische Detailangaben
Hauptverfasser: RALPH P. VOLANTE, KAI ROSSEN, JESS W. SAGER, PAUL J. REIDER, DAVID ASKIN
Format: Patent
Sprache:eng
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Zusammenfassung:A process for making a clinically efficacious HIV protease inhibitor Compound J eliminates one step in its synthesis, by an improved, alternative synthesis of the 2(S)-4-picolyl-2-piperazine-t-butyl-carboxamide intermediate.