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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359006Generated: October 30, 2026

Water → 4-(1-phenyl-1H-indazol-3-yl)-1-piperazine carboxylic acid ethyl ester

https://huagongshe.com/reaction/359006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-[(Phenylhydrazono)(2-fluorophenyl)methyl]-1-piperazine carboxylic acid ethyl esterHCID 54290288—
SolventTetrahydrofuranHCID 8028—
Product4-(1-phenyl-1H-indazol-3-yl)-1-piperazine carboxylic acid ethyl esterHCID 1511707351%

Reaction Steps

To a stirred solution, under nitrogen of 16.2 g of 4-[(phenylhydrazono)(2-fluorophenyl)methyl]-1-piperazine carboxylic acid ethyl ester in 150 ml of tetrahydrofuran was added, dropwise, a solution of 6.0 g of potassium t-butoxide in 60 ml of tetrahydrofuran. The reaction mixture was stirred at room temperature for 16 hrs., poured into water, and extracted with dichloromethane. The extract was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated to an oil. The oil was purified on a Water's Model 500 Preparative High Pressure Liquid Chromatograph utilizing two silica gel columns and hexane/ethyl acetate (3:1 by volume) as the eluent. Concentration of the appropriate fractions yielded 5.3 g (51%) of 4-(1-phenyl-1H-indazol-3-yl)-1-piperazine carboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04999356
Source datasetuspto-grants-1991_03
ORD IDord-2e1ceb4d20d9422eb7d9154bef5886cb
Source noteuspto-grants-1991_03