NEW 2-HYDRAZONOPHENYLTHIOACETAMIDES INTERMEDIATES IN THE SYNTHESIS OF 6-ACYLAMINO-3,6- DIHYDRO-2H-1,3,4-THIADIAZINES
摘要:
The three steps synthesis of new 2-hydrazonophenylthioacetamides having a N-monosubstitued thioamide group is described. The selective acylation of the thioamide nitrogen atom involves an intramolecular cyclisation affording 3,6-dihydro-2H-1,3,4-thiadiazines with good yields.
NEW 2-HYDRAZONOPHENYLTHIOACETAMIDES INTERMEDIATES IN THE SYNTHESIS OF 6-ACYLAMINO-3,6- DIHYDRO-2H-1,3,4-THIADIAZINES
作者:M. J. Gil、A. Reliquet、J. C. Meslin
DOI:10.1080/10426509708043544
日期:1997.7.1
The three steps synthesis of new 2-hydrazonophenylthioacetamides having a N-monosubstitued thioamide group is described. The selective acylation of the thioamide nitrogen atom involves an intramolecular cyclisation affording 3,6-dihydro-2H-1,3,4-thiadiazines with good yields.
Gil, M. J.; Reliquet, A.; Reliquet, F., Phosphorus, Sulfur and Silicon and the Related Elements, 1994, vol. 97, # 1-4, p. 89 - 94
作者:Gil, M. J.、Reliquet, A.、Reliquet, F.、Meslin, J. C.