Preparation and Reaction of 3-Oxo-3H-pyrazolo[1,5-a]indole Derivatives
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概要
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An alternative method to prepare 3-oxo-2-phenyl-3H-pyrazolo[1,5-a]indoles starting from indoline-2-carboxylic acid was explored. The reaction with nucleophilic agents allowed us to introduce the properly substituted alkyl substituents at C-4 of the 4H-pyrazolo[1,5-a]indoles. The 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) oxidation of these products gave the 3-oxo-2-phenyl-3H-pyrazolo[1,5-a]indole derivatives. Selective Keto-enol tautomerizations of these 1,5-diketo-monoene system were observed.
- 社団法人日本薬学会の論文
- 1994-02-15
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