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Synthesis 2006(3): 461-466
DOI: 10.1055/s-2006-926284
DOI: 10.1055/s-2006-926284
PAPER
© Georg Thieme Verlag Stuttgart · New York
Amidination of Amines under Microwave Conditions Using Recyclable Polymer-Bound 1H-Pyrazole-1-carboxamidine
Further Information
Received
18 July 2005
Publication Date:
11 January 2006 (online)
Publication History
Publication Date:
11 January 2006 (online)
Abstract
A convenient one-step transformation of primary and secondary amines into the corresponding unprotected guanidines using 4-benzyl-3,5-dimethyl-1H-pyrazole-1-carboxamidine and its polymer-bound variant is described. The scopes and limitations of the method, the microwave-assistance of amidination as well as a recycling protocol are examined.
Key words
amines - guanidines - polymer-bound reagent - microwave-assisted synthesis - reagent regeneration
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References
We first tested this transformation with 3-benzylpentane-2,4-dione which was treated with H2NNH2·H2O (CH2Cl2, r.t., 24 h) to yield 2a. Then the resulting pyrazole was transformed into 1a (91%) with cyanamide (anhyd dioxane, 120 °C, 4 h).