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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574251Generated: October 30, 2026

Ethanolamine → ((R)-2-{3-(2,6-difluoro-benzyl)-5-[2-(2-hydroxy-ethylamino)-acetylamino]-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl}-1-phenyl-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/574251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantTriethylamineHCID 8471—
Reactant{(R)-2-[5-(2-chloro-acetylamino)-3-(2,6-difluoro-benzyl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl esterHCID 67143301—
SolventAcetonitrileHCID 6342—
Product((R)-2-{3-(2,6-difluoro-benzyl)-5-[2-(2-hydroxy-ethylamino)-acetylamino]-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl}-1-phenyl-ethyl)-carbamic acid tert-butyl esterHCID 6714350380.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of {(R)-2-[5-(2-chloro-acetylamino)-3-(2,6-difluoro-benzyl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester (44 mg, 0.08 mmol) in acetonitrile (2 mL) were added triethylamine(30 μl, 0.22 mmol) and 2-amino-ethanol (60 μl, 0.96 mmol) in that order. The solution was stirred at 60° C. for 4 hrs, cooled to room temperature, and washed with an aqueous saturated sodium bicarbonate solution to separate an organic layer. The organic layer was concentrated, and the residue was purified using silica gel chromatography (eluent: dichloromethane/methanol, 10/1) and dried in a vacuum to afford 37 mg of the compound as a colorless oil (yield 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034850B2
Source datasetuspto-grants-2015_05
ORD IDord-9359df1abec641e0b70feea240be14ea
Source noteuspto-grants-2015_05