23614-55-3Relevant academic research and scientific papers
1,2-DIACYL-1-ARYLHYDRAZINES. 1. DERIVATIVES OF 2-HYDROXY- AND 2-HALOGENOBENZOIC ACIDS
Buzykin, B. I.,Sysoeva, L. P.
, p. 1115 - 1120 (2007/10/02)
New 1,2-diacyl-1-arylhydrazines, containing a hydroxy group or a mobile halogen atom in the 1-acyl fragment, were obtained by the reaction of the arylhydrazones of acetyl and benzoyl chlorides with the salts of 2-hydroxy-, 2-acetoxy-, and 2-halogeno-3-nitrobenzoic acids. 1-(2-Hydroxybenzoyl)-1-aryl-2-acylhydrazines could not be converted into cyclic products.On heating in alkaline and acidic media elimination of the more hindered salicyloyl group and not dehydration occurred.When boiled in DMF in the presence of bases, 1-(2-halogeno-3-nitro-5-R-benzoyl)-1-aryl-2-acylhydrazines gave 2-aryl-5-R-7-nitroindazol-3-ones and not the expected 4,5-dihydrobenzo-1,3,4-oxadiazepin-5-ones. Keywords: 1,2-Diacyl-1-arylhydrazines, salicylic acid, nitrohalogenobenzoic acids, 2-aryl-7-nitroindazol-3-ones, Chattaway-Walker reaction.
Displacement-Cyclization Reactions of Mono-substituted Hydrazines With Chloronitrobenzenes and Chloronitropyrimidines. New Routes to 8-Azapurine and Benzopyrazole Derivatives
DeFusco, A.A.,Strauss, M.J.
, p. 351 - 355 (2007/10/02)
Reactions of different chloronitrobenzenes and chloronitropyrimidines with monosubstituted hydrazines, R-NHNH2, where R is methyl, carbomethoxy and phenyl, are described.The reactivity of these hydrazines in displacement -ortho substituent cyclizations va
