通过肼与α-氨基酯衍生的异氰酸酯缩合合成 3-氨基海因的新方法

IF 2 Q2 CHEMISTRY, ORGANIC
SynOpen Pub Date : 2023-12-11 DOI:10.1055/a-2217-6821
Houda Bouchnak, Thierry Ollevier, Jamil Kraïem
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引用次数: 0

摘要

据报道,一种新的、简单而高效的 3-氨基海因合成方法从相应的 l-氨基酯开始,分两个步骤进行。市售的α-氨基酯被转化为相应的异氰酸酯衍生物,然后在 DMAP 和 DIPEA 的存在下,与水合肼和芳基肼发生缩合反应。这种方法以简单实用的方案提供了相应的 3-氨基海因,产量适中且良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

New Synthesis of 3-Aminohydantoins via Condensation of Hydrazines with Isocyanates Derived from α-Amino Esters

New Synthesis of 3-Aminohydantoins via Condensation of Hydrazines with Isocyanates Derived from α-Amino Esters

A new, simple, and efficient method for the synthesis of 3-aminohydantoins was reported in two steps, starting from the corresponding l -amino esters. Commercially available α-amino esters were converted into the corresponding isocyanate derivatives, which were then subjected to the condensation reaction with hydrazine hydrate and arylhydrazines, in the presence of DMAP and DIPEA. This method provides the corresponding 3-aminohydantoins in moderate and good yields under a simple and practical protocol.

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来源期刊
SynOpen
SynOpen CHEMISTRY, ORGANIC-
CiteScore
2.30
自引率
4.00%
发文量
35
审稿时长
6 weeks
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