The present investigation is related to the construction of
novel 3-(3-bromophenyl)-2-(1,3-diphenyl-1H-pyrazol-4-yl)acrylic acid by
reacting methyl 1,3-diphenyl-1H-pyrazole-4-carboxylate with 3-bromophenyl
aldehyde. The hydrazone prepared from acetophenone and phenyl hydrazine was
subjected to the Vilsmeier-Haack reagent and after the usual workup, 4-formyl
pyrazole was obtained. The 4-formylpyrazole was further converted into methyl
pyrazole-4-carboxylate via various intermediates such as
(1,3-diphenyl-1H-pyrazol-4-yl)methanol,
4-(chloromethyl)-1,3-diphenyl-1H-pyrazole, and
2-(1,3-diphenyl-1H-pyrazol-4-yl)acetonitrile. The methyl
1,3-diphenyl-1H-pyrazole-4-carboxylate is a key scaffold that was further used
for Knoevenagel condensation with substituted aldehydes to get the
(pyrazol-4-yl)acetic acid derivatives. All intermediates and the final target
were characterized by their spectral data.
Author(s) Details:
Karan Singh,
Department of Chemistry, Indira Gandhi University, Meerpur,
Rewari-122502, Haryana, India.
Harshita Phougat
Department of Chemistry, Indira Gandhi University, Meerpur, Rewari-122502,
Haryana, India.
Please see the link here: https://stm.bookpi.org/CICMS-V9/article/view/14337
No comments:
Post a Comment