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Structure-activity relationships in the formation of amides from substitutedN-benzylanilines

 

作者: UlgenM.,   GorrodJ. W.,   BarlowD.,  

 

期刊: Xenobiotica  (Taylor Available online 1994)
卷期: Volume 24, issue 8  

页码: 735-748

 

ISSN:0049-8254

 

年代: 1994

 

DOI:10.3109/00498259409043274

 

出版商: Taylor&Francis

 

数据来源: Taylor

 

摘要:

1. Thein vitrohepatic microsomal metabolism of certain substitutedN-benzylanilines was studied in the male hamster to establish the mechanism(s) and process(es) involved in the formation of the corresponding amides.2.N-Benzyl-2,4,6-trihalogeno,N-benzyl-4-cyano- andN-benzyl-4-nitroanilines were only metabolized byN-debenzylation. However,N-benzyl-4-methyl- andN-benzyl-2,4,6-trimethylanilines gave rise to both the corresponding amide and nitrone metabolites together with dealkylation products. These latter two substrates also produced hydroxymethyl metabolites as major products. Metabolism ofN-(2,4,6,-trimethylbenzyl)aniline also led to the formation of an amide metabolite. The dealkylation products, the corresponding imine and an unknown metabolite, probably an hydroxylated product were also detected with this substrate.3.N-(2,4-Dichlorobenzyl) andN-(2,6-dichlorobenzyl) anilines yielded the corresponding nitrone metabolites; but no amide metabolite was detected. Oxidative dealkylation leading to the formation of the corresponding primary anilines and aldehydes, together withparahydroxylation of aniline rings, were established as major routes of metabolism for both compounds. Similarly, neitherN-(2,4,6-triflurobenzyl) norN-(4-nitrobenzyl) anilines produced any amide metabolite although dealkylation products were detected.4. The pattern of amide formation observed for theseN-benzylsubstituted anilines is discussed in terms of the steric and electronic effects of their aromatic substituents.

 

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