J. Grote, Yon-Yih Chen
Jan 15, 2014
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Journal
Tetrahedron Letters
Abstract
Abstract An efficient synthesis of a chemiluminescent valproic acid conjugate is described. Reaction of diethyl propylmalonate with 4-bromobutylphthalimide produced an amino protected malonate, which was deprotected with hydrazine and treated with HCl to produce an aminoderivatized valproic acid. Reaction with an acridinium active ester produced the conjugate in good yield. Careful selection of commercially available materials and mild conditions made this pathway amenable to scale up. This strategy offers a general method for the preparation of valproic acid conjugates.