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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454982Generated: October 30, 2026

Bromide ion → t-Butyl (1R)-1-(4-(2-methylpentyloxy)phenyl)-2-(4-methylpiperazin-1-yl)ethylcarbamate

https://huagongshe.com/reaction/454982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantPotassium CarbonateHCID 11430—
Reactant[(R)-1-(4-Hydroxy-phenyl)-2-(4-methyl-piperazin-1-yl)-ethyl]-carbamic acid tert-butyl esterHCID 58459801—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productt-Butyl (1R)-1-(4-(2-methylpentyloxy)phenyl)-2-(4-methylpiperazin-1-yl)ethylcarbamateHCID 67430949—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of [(R)-1-(4-hydroxy-phenyl)-2-(4-methyl-piperazin-1-yl)-ethyl]-carbamic acid tert-butyl ester (57 mg, 0.17 mmol), K2CO3 (72 mg, 0.52 mmol) and 2-methylpenthyl bromide (60 ul, 0.42 mmol) in DMF (1 ml) was stirred at 55° C. for over night. After cool to rt, the mixture was diluted with EtOAc and washed with H2O and dried (MgSO4). Removal of the solvent provided the titled compound. MS (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497271B2
Source datasetuspto-grants-2013_07
ORD IDord-79db1b79f5d5410a828e622afbb15db1
Source noteuspto-grants-2013_07