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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450864Generated: October 30, 2026

Phenyl chloroformate → 1-Benzenesulfonyl-3-(1-phenoxycarbonyl4-piperazinyl)-1H-indazole

https://huagongshe.com/reaction/1450864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
Reactant1-(Benzenesulfonyl)-3-(4-methylpiperazin-1-yl)-1H-indazoleHCID 14823425—
SolventDichloromethaneHCID 6344—
Product1-Benzenesulfonyl-3-(1-phenoxycarbonyl4-piperazinyl)-1H-indazoleHCID 1846722355.1%

Reaction Steps

To a solution of 1-benzenesulfonyl-3-(1-methyl-4-piperazinyl)-1H-indazole (2.1 g, 5.89 mmol) in dichloromethane (100 ml) was added phenyl chloroformate (3.8 ml, 29.45 mmol) at room temperature. The reaction mixture was warmed to reflux for 2 hours, cooled to room temperature, and concentrated. The residue was diluted with ethyl acetate, filtered and purified via flash column chromatography (silica gel, ethyl acetate). Concentration of the product containing fractions gave an oil which solidified on standing. The product was washed well with heptane to give 1.5 g of a white solid, m.p. 112°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602159
Source datasetuspto-grants-1997_02
ORD IDord-63ca886941314ddf8bdd846fbf6eb3ea
Source noteuspto-grants-1997_02