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Progress in arylpiperazine synthesis by the catalytic amination reaction. | LitMetric

Progress in arylpiperazine synthesis by the catalytic amination reaction.

Bioorg Med Chem

Process Research Laboratory, Second Tokushima Factory, Otsuka Pharmaceutical Co. Ltd., Kawauchi-cho, Tokushima, Japan.

Published: December 2002

Careful base and solvent optimization for catalytic amination is described. A Pd-catalyzed amination between some arylbromide and unprotected piperazine (1equiv) was efficiently carried out with Pd/BINAP catalyst in a toluene-DBU solvent system, which is useful for the one-pot preparation of unsymmetrical piperazine through amination and in-situ N-protection. Reaction with N-BOC-piperazine was also successful in toluene-DBU or more polar NMP with Cs(2)CO(3) as a key base. No reports have previously reported such solvent and base optimization in arylpiperazine synthesis.

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http://dx.doi.org/10.1016/s0968-0896(02)00303-6DOI Listing

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