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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365580Generated: October 29, 2026

Pyridine → HCID 22716470, compound

https://huagongshe.com/reaction/1365580

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 numberUS07892574B2
Source datasetuspto-grants-2011_02
ORD IDord-a2cc73f6e90f4e66853c6933260ae822
Source noteuspto-grants-2011_02