<i>N</i>-ALKOXY-<i>N</i>-CHLOROUREAS IN THE SYNTHESIS OF 3,4-DIHYDRO-1<i>H</i>-2,1-BENZOXAZINE-1-CARBOXAMIDE AND 1-ALKOXY-1,3-DIHYDROBENZIMIDAZOL-2-ONES
DOI:
https://doi.org/10.1007/421Keywords:
N-alkoxy-N-chloroureas, 1-alkoxy-1, 3-dihydrobenzimidazol-2-ones, 3, 4-dihydro-1H-2, 1-benzoxazine-1-carboxamide, nitrogen-containing heterocycles, cyclizationAbstract
The cyclization of N-chloro-N-(2-phenylethoxy)urea in the presence of silver trifluoroacetate leads to the formation of 3,4-dihydro-1H-2,1-benzoxazine-1-carboxamide, while N-alkoxy-N'-aryl-N-chloro-ureas in the presence of sodium acetate form 1-alkoxy-1,3-dihydrobenzimidazol-2-ones. The structures of 3,4-dihydro-1H-2,1-benzoxazine-1-carboxamide and 1-methoxy-6-nitro-1,3-dihydrobenzimidazol-2 one were examined by X-ray structural analysis.
Authors: V. G. Shtamburg, O. V. Shishkin, V. V. Shtamburg, R. I. Zubatyuk, A. V. Mazepa, and R. G. Kostyanovsky.
English Translation in Chemistry of Heterocyclic Compounds, 2013, 49 (8), pp 1195-1206