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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166015Generated: November 1, 2026

Pyridine → HCID 22716470, compound

https://huagongshe.com/reaction/1166015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 22716472HCID 22716472—
SolventDichloromethaneHCID 6344—
ProductHCID 22716470HCID 22716470—

Reaction Steps

5-Amino-2-(4-[2-fluoroethyl]-3-oxopiperazin-1-yl)fluorobenzene (2.6 g) is dissolved in dry dichloromethane (50 ml) under argon. Pyridine (1.03 ml) is added, and the mixture cooled to −20°. Benzyl chloroformate (1.6 ml) is added and the mixture stirred for 10 minutes at −20°, before allowing the temperature to rise to 20-25° over 1.5 hours. The solvents are removed and the residue is dissolved in dichloromethane and washed with sodium bicarbonate solution. After drying over magnesium sulfate and removal of the solvent, the residue is chromatographed (silica, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane) to give 5-benzyloxycarbonylamino-2-(4-[2 fluoroethyl]-3-oxopiperazin-1-yl)fluorobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613349B2
Source datasetuspto-grants-2003_09
ORD IDord-5418e27c15424567a53bad89f2b9a485
Source noteuspto-grants-2003_09