Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370235Generated: October 30, 2026

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

https://huagongshe.com/reaction/370235

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 numberUS06140345
Source datasetuspto-grants-2000_10
ORD IDord-e568a6f783004e2680dcdc1d849fc758
Source noteuspto-grants-2000_10