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Some Cyclization Reactions with 1,3‐Diphenyl‐5‐Imino‐2‐Imidazolidinone‐4‐Thione
Author(s) -
Mohamed Y.A.,
Ammar Y.A.,
Sh. ElSharief A.M.,
Aly M.M.
Publication year - 1990
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.199000070
Subject(s) - chemistry , semicarbazone , bromide , medicinal chemistry , condensation , condensation reaction , organic chemistry , catalysis , physics , thermodynamics
1,3‐Diphenyl‐5‐imino‐2‐imidazolidinone‐4‐thione (II) was treated with diazomethanes to give (III‐V). Interaction of (II) with amino compounds furnished the corresponding 4‐substituted imino derivatives (VIa‐m). Imidazoquinoxaline derivatives (VIIIb, c) were obtained through interaction of (II) with o‐phenylenediamines. Condensation of (II) with hydrazines afforded the hydrazones (IX, Xa, b). Semicarbazone and thiosemicarbazone derivatives (XIIa‐d) were prepared from the reaction of (IX) with isocyanates and isothiocyanates. Again (II) was allowed to react with n‐butylmagnesium bromide and HgCl 2 to give (XIII) and (XIV) respectively.
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