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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082713Generated: October 28, 2026

Phenyl chloroformate → HCID 18467270, compound

https://huagongshe.com/reaction/1082713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
Reactant1-benzoyl-6-fluoro-3-(1-methyl-4-piperidinyl)-1H-indazoleHCID 14032555—
SolventDichloromethaneHCID 6344—
ProductHCID 18467270HCID 1846727017.9%

Reaction Steps

To a solution of 1-benzoyl-6-fluoro-3-(1-methyl-4-piperidinyl)-1H-indazole (2.0 g, 5.93 mmol) in dichloromethane (100 ml) was added phenyl chloroformate (3.9 ml, 29.65 mmol) at room temperature. The reaction mixture was stirred at room temperature for 24 hours, refluxed for an additional 0.5 hours and subsequently concentrated. The remaining residue was dissolved into dichloromethane and washed with 10% HCl (aq.). The organic phase was dried (MgSO4), filtered, and concentrated to give an oil which was purified via flash column chromatography (silica gel, 20% DCM/EtOAc). Concentration of the product-containing fractions gave an oil which solidified on standing. The white solid was washed with EtOAc, leaving 0.47 g of the desired product, m.p. 137°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589495
Source datasetuspto-grants-1996_12
ORD IDord-59b60e9e4d94461f9e1fc2780264d7d0
Source noteuspto-grants-1996_12