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
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.