Reactions of 4-benzoyl-1,5-diphenyl-1H-pyrazole-3- carboxylic acid chloride with various hydroxylamines and carbazates

Authors

ELİF KORKUSUZ
İSMAİL YILDIRIM

DOI

10.3906/kim-1004-523

Abstract

The 1H-pyrazole-3-carboxylic acid 2 was converted via reactions of its acid chloride 3 with various hydroxylamine 4a-f and carbazate derivatives 8a-c into the corresponding novel N-substituted-4-benzoyl-1,5-dipenyl-1H-pyrazole-3-carboxamides 5a-c, N,N-disubstituted-4-benzoyl-1,5-diphenyl-1H-pyrazole-3-carboxylates 6d,e, 4-benzoyl-N-{[(4-benzoyl-1,5-diphenyl-1H-pyrazol-3-yl)carbonyl]oxy}- N-methyl-1,5dip- henyl-1H-pyrazole-3-carboxamide (7), and 4-benzoyl-N'-(alkoxycarbonyl)-1,5-diphenyl-1H-pyrazole-3-car- bohydrazides 9a,b and 10, respectively, in good yields (65\%-90\%). The reactions of 3 with 4 and 8 in xylene for 8-15 h with catalytic amounts of base led to the formation of the products 5-7, 9, and 10. The structures of all new synthesized compounds were established by the ^{13}C-NMR, ^1H-NMR, IR spectroscopic data, and elemental analyses.

Keywords

Pyrazole-3-carboxylic acid, nucleophilic substitution, furan-2, 3-dione, carbazate, hydroxylamine

First Page

859

Last Page

868

Recommended Citation

KORKUSUZ, ELİF and YILDIRIM, İSMAİL (2010) "Reactions of 4-benzoyl-1,5-diphenyl-1H-pyrazole-3- carboxylic acid chloride with various hydroxylamines and carbazates," Turkish Journal of Chemistry: Vol. 34: No. 6, Article 3. https://doi.org/10.3906/kim-1004-523
Available at: https://journals.tubitak.gov.tr/chem/vol34/iss6/3