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Preparation of 1H-pyrazole-5-carboxamides from dilithiated C(α), N-phenylhydrazones and lithiated ethyl oxanilates or lithiated ethyl oxamate

✍ Scribed by Jennifer R. Downs; Stefan J. Pastine; Deborah A. Schady; Heather A. Greer; Wayne Kelley Jr.; Mildred C. Embree; Jessica D. Townsend; Charles F. Beam


Publisher
Journal of Heterocyclic Chemistry
Year
2001
Tongue
English
Weight
39 KB
Volume
38
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

Dilithiated C(α), N‐phenylhydrazones were prepared in excess lithium diisopropylamide and condensed with either ethyl oxanilate, ethyl 4′‐chlorooxanilate, or ethyl oxamate to give intermediates that were quenched and acid cyclized to substituted l__H__‐pyrazole‐5‐carboxamides.


📜 SIMILAR VOLUMES


Preparation of 2-(1-phenyl-1H-pyrazol-5-
✍ Michelle A. Meierhoefer; S. Patrick Dunn; Laela M. Hajiaghamohseni; Matthew J. W 📂 Article 📅 2005 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 92 KB

Select C(α),N-phenylhydrazones were dilithiated in excess lithium diisopropylamide followed by condensation with methyl 2-(aminosulfonyl)benzoate and acid cyclization to afford new pyrazol-benzenesulfonamides, 2-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamides.