Issue 10, 1998

Reaction of Symmetric N1,N2-Diarylamidines with α-Bromoacetophenone and Ethyl 2-Bromoethanoate

Abstract

2-Bromo-1-{aryl[1-(arylimino)ethyl]amino}-1-phenylethanol derivatives 3a, 3b were obtained from the reaction of N1,N2-diarylacetamidines 1a, 1b with α-bromoacetophenone 2, while 1a, 1b with ethyl 2-bromoethanoate 4 afforded 2-{[1-(arylimino)]ethyl}aminoethanoic acid derivatives 5a, 5b; N1,N2-diarylformamidines 6a, 6b reacted with 2 and 4 to give the arylaminoacetophenones 8a, 8b and N-arylglycine ethyl esters 11a, 11b respectively together with the corresponding formanilides 9a, 9b.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 654-655

Reaction of Symmetric N1,N2-Diarylamidines with α-Bromoacetophenone and Ethyl 2-Bromoethanoate

M. Abdel-Motaal Gomaa, J. Chem. Res. (S), 1998, 654 DOI: 10.1039/A802858C

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