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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324785Generated: October 25, 2026

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

https://huagongshe.com/reaction/324785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,4-DichlorobenzaldehydeHCID 22710—
Reactant4-Chlorobenzene-1-carboximidamide hydrochlorideHCID 203436—
Reactant3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
SolventDimethylformamideHCID 6228—
Product3-Phenylpropyl 2-(4-chlorophenyl)-4-(3,4-dichlorophenyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylateHCID 220055203%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (5.46 g, 15.70 mmol), 3,4-dichlorobenzaldehyde (2.75 g, 15.70 mmol), 4-chlorobenzamidine hydrochloride (3.0 g, 15.70 mmol) and potassium carbonate (2.17 g, 15.70 mmol) was stirred in N,N-dimethylformamide (15 ml) for 5 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 (300 mg) as an oil. Electrospray MS m/z 640/642 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218538B1
Source datasetuspto-grants-2001_04
ORD IDord-b512d2d240a34d0e8f796183c5d0b819
Source noteuspto-grants-2001_04