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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357436Generated: October 30, 2026

Phenyl chloroformate → HCID 18467270, compound

https://huagongshe.com/reaction/357436

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 numberUS05840727
Source datasetuspto-grants-1998_11
ORD IDord-1cea96c48cbd456f858be1ed3536a8e4
Source noteuspto-grants-1998_11