Preparation of 2-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamides from polylithiated C(α),N-phenylhydrazones and methyl 2-(aminosulfonyl)benzoate
✍ Scribed by Michelle A. Meierhoefer; S. Patrick Dunn; Laela M. Hajiaghamohseni; Matthew J. Walters; Mildred C. Embree; Sally P. Grant; Jennifer R. Downs; Jessica D. Townsend; Clyde R. Metz; Charles F. Beam; William T. Pennington; Donald G. VanDerveer; N. Dwight Camper
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 92 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
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.
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## Abstract magnified image Select C(α), __N__‐carbo‐__tert‐__butoxyhydrazones were dilithiated with excess lithium diisopropylamide followed by condensation with methyl 2‐(aminosulfonyl)benzoate, acid cyclization, hydrolysis, and decarboxylation to afford new 2‐(1__H__‐pyrazol‐5‐yl)benzenesulfona
## Abstract magnified image A variety of substituted spiro(benzoisothiazole‐pyrazoles) have been prepared by the condensation of dilithiated __C__(α),__N__‐carboalkoxyhydrazones with lithiated methyl 2‐(aminosulfonyl)benzoate followed by the cyclization of intermediates with acetic anhydride, whic
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