13958-22-0Relevant academic research and scientific papers
2-thiophenecarbohydrazides: A novel efficient method for the synthesis of 2-thiophenecarbohydrazide
Elshaarawy, Reda F.M.,Janiakb, Christoph
experimental part, p. 1202 - 1208 (2012/03/09)
Hydrazinolysis of carboxylic acid esters in alcoholic solutions is the standard method for preparing carbohydrazides (carboxylic hydrazides). Here we report an efficient process, involving the reaction of activated esters or amides with hydrazine, for the preparation of thiophenecarbohydrazides in yields larger than 90% and high purity. With this new method, a series of heteroaryl-, aryl-, or aralkyl- substituted carbohydrazides were synthesized and characterized. The X-ray crystal structure of 2-thiophenecarbohydrazide (thiophene-2-carboxylic hydrazide, 2-thenoyl-hydrazine) has revealed that it crystallizes in the monoclinic system, space group P21/c, with cell parameters of a = 6.1202(2), b = 8.3907(3), c = 12.5332(5) A, β = 98.6577(11)?, Z = 4, R(F) = 0.0455 and wR(F2) = 0.1805, T = 293 K.
Electrochemical reduction of N-acylureas
Quintanilla, M. Gloria,Montero, Guillermo,Hierro, Angel G.,Diaz, Jose M.,Bassani, Silvina
, p. 928 - 931 (2007/10/03)
The cathodic reduction of N-acylureas with the structure R-NH-CO-N(COR′)-R in an aprotic medium gives N-alkylamides (R′-CO-NH-R) and amines (R-NH2) in a selective cleavage process. The structure of the R′ group is a significant factor of the el
