Singh_2008_Beilstein.J.Org.Chem_4_20

Reference

Title : Synthesis of (S)-1-(2-chloroacetyl)pyrrolidine-2-carbonitrile: a key intermediate for dipeptidyl peptidase IV inhibitors - Singh_2008_Beilstein.J.Org.Chem_4_20
Author(s) : Singh SK , Manne N , Pal M
Ref : Beilstein J Org Chem , 4 :20 , 2008
Abstract :

An alternative and practical synthesis of (S)-1-(2-chloroacetyl)pyrrolidine-2-carbonitrile was achieved. Reaction of L-proline with chloroacetyl chloride was followed by conversion of the carboxylic acid moiety of the resulting N-acylated product into the carbonitrile via the corresponding amide intermediate. The synthesized pyrrolidine derivative was utilized to prepare DPP-IV inhibitor Vildagliptin.

PubMedSearch : Singh_2008_Beilstein.J.Org.Chem_4_20
PubMedID: 18941490

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Citations formats

Singh SK, Manne N, Pal M (2008)
Synthesis of (S)-1-(2-chloroacetyl)pyrrolidine-2-carbonitrile: a key intermediate for dipeptidyl peptidase IV inhibitors
Beilstein J Org Chem 4 :20

Singh SK, Manne N, Pal M (2008)
Beilstein J Org Chem 4 :20