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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324781Generated: October 25, 2026

3,4-Dichlorobenzaldehyde → 3-Phenylpropyl 4-(3,4-dichlorophenyl)-2-phenyl-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/324781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorobenzaldehydeHCID 22710—
ReactantBenzamidine, hydrochlorideHCID 80289—
ReactantSodium AcetateHCID 517045—
Reactant3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
SolventDimethylformamideHCID 6228—
Product3-Phenylpropyl 4-(3,4-dichlorophenyl)-2-phenyl-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylateHCID 220055302.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (1.50 g, 4.32 mmol), 3,4-dichlorobenzaldehyde (0.907 g, 5.18 mmol), benzamidine hydrochloride (0.811 g, 5.18 mmol) and sodium acetate (0.425 g, 5.18 mmol) was stirred in N,N-dimethylformamide (10 mL) for 14 days at room temperature and then heated to 60° C. for 3 days. The DMF was removed in vacuo and ethyl acetate was added to the residue. The precipitate was removed by filtration and the filtrate was washed with water, sodium hydrogen carbonate solution and brine, dried and evaporated to yield an oil. The oil was further purified by flash chromatography and RP-HPLC to give the title compound (60 mg) as an oil. Electrospray MS m/z 606/608 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218538B1
Source datasetuspto-grants-2001_04
ORD IDord-ae5a80fb576c4a2e922d506fe841ee4e
Source noteuspto-grants-2001_04