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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108587Generated: October 30, 2026

Pyridine → 5-Benzyloxycarbonylamino-2-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)fluorobenzene

https://huagongshe.com/reaction/1108587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl chloroformateHCID 10387—
Reactant5-Amino-2-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)fluorobenzeneHCID 18783902—
SolventDichloromethaneHCID 6344—
Product5-Benzyloxycarbonylamino-2-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)fluorobenzeneHCID 18783906—

Reaction Conditions

Temperature-20 °C

Reaction Steps

5-Amino-2-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)fluorobenzene (3.5 g) was dissolved in dry dichloromethane (50 ml) under argon. Pyridine (1.33 ml) was added, and the mixture cooled to -20° C. Benzyl chloroformate (2.06 ml) was added, and the mixture stirred for 10 minutes at -20° C., before allowing the temperature to rise to ambient over 1.5 hours. Solvents were evaporated, the residue dissolved in dichloromethane and washed with sodium bicarbonate solution. After drying (MgSO4) and evaporation of solvent, the residue was chromatographed on silica, using as eluant a gradient increasing in polarity from 0 to 4% methanol in dichloromethane. Relevant fractions were combined and evaporated to give 5-benzyloxycarbonylamino-2-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)fluorobenzene (3.28 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069145
Source datasetuspto-grants-2000_05
ORD IDord-63f7b243b9444ded82b59f57879b9c03
Source noteuspto-grants-2000_05