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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324778Generated: October 26, 2026

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

https://huagongshe.com/reaction/324778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorobenzaldehydeHCID 22710—
ReactantSodium AcetateHCID 517045—
ReactantPyridine-4-amidine hydrochlorideHCID 2776844—
Reactant3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
SolventDimethylformamideHCID 6228—
Product3-Phenylpropyl 4-(3,4-dichlorophenyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-2-(4-pyridyl)-1,4-dihydropyrimidine-5-carboxylateHCID 220055313.1%

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), 4-amidinopyridine hydrochloride (0.816 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 6 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 to give the title compound (81.7 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218538B1
Source datasetuspto-grants-2001_04
ORD IDord-76d939b350284a8cb06b7161a68ee743
Source noteuspto-grants-2001_04