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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108570Generated: October 29, 2026

N,N-Dimethylaniline → 5-Benzyloxycarbonylamino-2-(4-methyl-3-oxopiperazin-1-yl)fluorobenzene

https://huagongshe.com/reaction/1108570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-(4-Amino-2-fluorophenyl)-1-methylpiperazin-2-oneHCID 18783930—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Benzyloxycarbonylamino-2-(4-methyl-3-oxopiperazin-1-yl)fluorobenzeneHCID 18783908—

Reaction Conditions

Temperature-20 °C

Reaction Steps

5-Amino-2-(4-methyl-3-oxopiperazin-1-yl)fluorobenzene (2.94 g) was dissolved in dry DMF (40 ml) under argon, and the solution cooled to -20° C. N,N-Dimethylaniline (2.1 ml) was added, followed by benzyl chloroformate (2.07 ml), and the mixture stirred for 10 minutes at -20° C. The temperature was allowed to rise to ambient over 16 hours. The mixture was diluted with ethyl acetate, and washed twice with water, and then brine. After drying (MgSO4) and evaporation of solvent, the residue was chromatographed on silica, using as eluant a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give 5-benzyloxycarbonylamino-2-(4-methyl-3-oxopiperazin-1-yl)fluorobenzene (4.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069145
Source datasetuspto-grants-2000_05
ORD IDord-d748b4cf864242f8a1950bc12750be38
Source noteuspto-grants-2000_05