81930-20-3Relevant academic research and scientific papers
2,4-Dialkyl Substituted Carbono- and Thiocarbonohydrazides, Reactions with Carbonyl Compounds
Neugebauer, Franz Alfred,Fischer, Hans,Siegel, Rolf,Krieger, Claus
, p. 3461 - 3481 (2007/10/02)
2,4-Dialkyl substituted carbono- and thiocarbonohydrazides (4) were prepared from alkylhydrazines and phosgene or thiophosgene.Mono carbonyl compounds reacted with 4 (molar ratio 1:1) to yield hexahydro-1,2,4,5-tetrazines (9, 14; exception 13).Aldehydes in excess generally afforded dihydrazones (3); formaldehyde, however, yielded 1,1'-methylenebis(hexahydro-1,2,4,5-tetrazines) (10) as well as the bicyclic compounds 11 and 12.The constitution of 11 was confirmed by X-ray analysis of 11b.Dialdehydes and aliphatic or alicyclic α-diketones reacted with 4 to give double hexahydro-1,2,4,5-tetrazine derivatives (19), aryl substituted α-diketones on the other hand yielded cyclic dihydrazones (15) and/or mono-hexahydro-1,2,4,5-tetrazines (16).
1,2,4,5-Tetrahydro-1,2,4,5-tetrazin-2,6-dione (p-Urazine) and Its Conversion into 1,2,4,5-Tetrazine Derivatives
Neugebauer, Franz Alfred,Fischer, Hans
, p. 387 - 395 (2007/10/02)
Cyclization of 4 with phosgene and subsequent hydrogenolysis of the protecting benzyl groups yielded the yet unknown p-urazine (1) which rearranges thermally to the tetrazolidine 2.Compound 1 was dehydrogenated to give 14 which exists in solution in the t
