A facile synthesis of piperazines from primary amines
DW Henry
Index: Henry,D.W. Journal of Heterocyclic Chemistry, 1966 , vol. 3, p. 503 - 511
Full Text: HTML
Citation Number: 20
Abstract
Abstract A general procedure is described for converting primary amines to N-substituted piperazines. Reaction of an amine with an N-substituted iminodiacetic acid anhydride (V) yields an iminodiacetic acid monoamide (VI) which closes to a 2, 6-piperazinedione (VII) upon treatment with acetic anhydride. The diones are reduced to piperazines with borane- THF. Fourteen examples of this process, using twelve aliphatic or aromatic amines and ...
Related Articles:
[Shudo, Koichi; Ohta, Toshiharu; Okamoto, Toshihiko Journal of the American Chemical Society, 1981 , vol. 103, # 3 p. 645 - 653]
[Ohwada, Atsushi; Li, Hao; Sakamoto, Takeshi; Kikugawa, Yasuo Heterocycles, 1997 , vol. 46, # 1 p. 225 - 233]