期刊
TETRAHEDRON LETTERS
卷 44, 期 24, 页码 4491-4493出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(03)00988-2
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Two simple Procedures for the selective protection of the ring N of aminopyrazoles as tert-butoxycarbamate (Boc) in high yields are reported: several other protecting groups (Cbz, Bn. SEM) can be introduced using the one-pot procedure (method B). The N-Boc protected aminopyrazoles are acylated at the exocyclic NH2 group and subsequently deprotected to give the corresponding 3-acylaminopyrazoles in high yields. This procedure is applicable for the rapid parallel synthesis of 3-acylaminopyrazoles. (C) 2003, Elsevier Science Ltd. All rights reserved.
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