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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250164Generated: October 31, 2026

Pyridine → HCID 22716470, compound

https://huagongshe.com/reaction/1250164

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 numberUS06337329B1
Source datasetuspto-grants-2002_01
ORD IDord-f2b74c598f5f46c79a787f44efe5faf6
Source noteuspto-grants-2002_01