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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261402Generated: November 1, 2026

1,2-Dichloroethane → n-Benzyloxy-3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionamide

https://huagongshe.com/reaction/2261402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
ReactantN,N-DiisopropylmethylamineHCID 547370—
Reactant3-(2-Oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionic acidHCID 11159560—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productn-Benzyloxy-3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionamideHCID 11391683268%

Reaction Steps

29 mg of 3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionic acid (g) was dissolved in 0.5 ml of DMF solution (0.171 mM). 30 mg of BnONH2.HCl (0.188 mmol), 0.033 ml of diisopropyl methylamine (0.189 mmol), 43 mg of EDC (0.224 mmol) and 5 mg of DMAP (0.041 mmol) were added thereto and the mixture was stirred for overnight at room temperature. The mixture was diluted with 7 ml of ethyl acetate and washed with 5% HCl (1 ml) and 1 ml of sat. NaHCO3 solution. The organic layer was dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting compound was purified by column chromatography on Silica gel with methanol/chloroform (1:20) solvent mixture as an eluant to give 126 mg (yield: 55%) of the title compound (h).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846963B2
Source datasetuspto-grants-2010_12
ORD IDord-dfd41532b9fa430b8601302f54e49966
Source noteuspto-grants-2010_12