Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708313Generated: October 28, 2026

Ethanolamine → Benzyl ((2R,3S)-1-(2,4-dimethoxybenzyl)-2-(((2-hydroxyethyl)amino)methyl)-4-oxoazetidin-3-yl)carbamate

https://huagongshe.com/reaction/708313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantDiisopropylethylamineHCID 81531—
Reactant((2S,3S)-3-(((benzyloxy)carbonyl)amino)-1-(2,4-dimethoxybenzyl)-4-oxoazetidin-2-yl)methyl methanesulfonateHCID 118379363—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductBenzyl ((2R,3S)-1-(2,4-dimethoxybenzyl)-2-(((2-hydroxyethyl)amino)methyl)-4-oxoazetidin-3-yl)carbamateHCID 11841132875.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ((2S,3S)-3-(((benzyloxy)carbonyl)amino)-1-(2,4-dimethoxybenzyl)-4-oxoazetidin-2-yl)methyl methanesulfonate (6.43 g, 13.4 mmol) in Acetonitrile (44.8 ml) was added ethanolamine (8.13 ml, 134 mmol) followed by DIPEA (7.0 ml, 40 mmol). The solution was heated to 80° C. for 20 h, whereupon it was cooled to rt, diluted with EtOAc, washed with water, dried over Na2SO4 and concentrated in vacuo, afford the title compound (4.47 g, 75%) as a white solid. LCMS: Rf=0.60 min, m/z=444.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-9de80c5160054881927df07c02795e9a
Source noteuspto-grants-2015_11