Synthesis of Formamidines from Carbodiimides with Sodium Borohydride in Isopropanol

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Abstract

Reduction of the N,N’-disubstituted carbodiimides with sodium borohydride in iso-propanol performs a convenient synthetic method of the corresponding formamidines. tert-Butanol, pyridine, and tetrahydrofuran proved also available as solvents for the procedure, while methanol or ethanol was unsuitable for the lower yield of the formamidine, probably due to the further reduction to proceed. © 1978, The Pharmaceutical Society of Japan. All rights reserved.

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Kaji, K., Matsubara, H., Nagashima, H., Kikugawa, Y., & Yamada, S. ichi. (1978). Synthesis of Formamidines from Carbodiimides with Sodium Borohydride in Isopropanol. Chemical and Pharmaceutical Bulletin, 26(7), 2246–2249. https://doi.org/10.1248/cpb.26.2246

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