POTENTIAL GABA-B RECEPTOR ANTAGONISTS .7. THE SYNTHESIS OF 2-(4-CHLOROPHENYL)-3-NITROPROPAN-1-AMINE AND RELATED ANALOGS OF BACLOFEN

被引:10
作者
ABBENANTE, G
HUGHES, R
PRAGER, RH
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D O I
10.1071/CH9941441
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
3-Nitro-2-phenylpropan-1-amine and 2-(4-chloropenyl)-3-nitropropan-1-amine have been synthesized by the addition of nitrous acid to the corresponding trifluoroacetylaminomethylstyrenes followed by reduction of the double bond with sodium borohydride. A more general and efficient route involves the Michael addition of nitroalkane anions to methyl cinnamates followed by Curtius degradation of the corresponding acids. 2-(4-Chlorophenyl)-3-nitropropan-1-amine is a specific agonist of GABA and the GABA(B) receptor, with about half the activity of racemic baclofen at the isolated guinea pig ileum. Methylation or dimethylation at C 3 decreases activity markedly.
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页码:1441 / 1452
页数:12
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