Preparation of 2-(1H-pyrazol-5-yl)benzenesulfonamides from polylithiated C(α),N-carbo-tert-butoxyhydrazones and methyl 2-(aminosulfonyl)benzoate
✍ Scribed by John D. Knight; Jordan B. Brown; Jason S. Overby; Charles F. Beam; N. Dwight Camper
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 408 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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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)benzenesulfonamides, [NH‐pyrazolyl‐ortho‐benzene‐sulfonamides].
📜 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.
## 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
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract magnified image Several dilithiated C(α), O‐oximes were prepared in excess lithium diisopropylamide‐tetramethyl‐ethylenediamine (LDA/TMEDA) and condensed with methyl **2**‐(aminosulfonyl)benzoate followed by acid cyclization of intermediates to spiro(benzoisothiazole‐isoxazole) dioxide