Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24600Generated: October 26, 2026

3,3-Diphenylpropylamine → 4-(3-Chlorophenyl)-6-methoxymethyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amide

https://huagongshe.com/reaction/24600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-DiphenylpropylamineHCID 79698—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(3-Chlorophenyl)-6-methoxymethyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acidHCID 22570146—
SolventDimethylformamideHCID 6228—
Product4-(3-Chlorophenyl)-6-methoxymethyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amideHCID 15546105—

Reaction Steps

130 mg (0.438 mmol) of 4-(3-chlorophenyl)-6-methoxymethyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid and 139 mg (0.657 mmol) of 3,3-diphenylpropylamine were dissolved in 10 ml of DMF. 126 mg (0.657 mmol) of WSC hydrochloride was added to the obtained solution under cooling with ice, and they were stirred at room temperature overnight. After the concentration under reduced pressure, the reaction mixture was diluted with ethyl acetate and then washed with 1 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (dichloromethane/methanol=50/1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855716B2
Source datasetuspto-grants-2005_02
ORD IDord-505e0b8c133c49b4b460c2aad404e340
Source noteuspto-grants-2005_02