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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324782Generated: October 30, 2026

4-Cyanobenzaldehyde → 3-Phenylpropyl 4-(4-cyanophenyl)-6-[(2-(N,N-diethylamino)ethoxy)methyl]-2-(2-furyl)-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/reaction/324782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium BicarbonateHCID 516892—
ReactantFuran-2-carboximidamide hydrochlorideHCID 12231049—
Reactant3-phenylpropyl 4-(2-(N,N-diethylamino)ethoxy)acetoacetateHCID 22005511—
SolventDimethylformamideHCID 6228—
Product3-Phenylpropyl 4-(4-cyanophenyl)-6-[(2-(N,N-diethylamino)ethoxy)methyl]-2-(2-furyl)-1,4-dihydropyrimidine-5-carboxylateHCID 2200556521.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-phenylpropyl 4-(2-(N,N-diethylamino)ethoxy)acetoacetate (2.0 g, 5.96 mmol), 4-cyanobenzaldehyde (0.86 g, 6.56 mmol), 2-amidinofuran hydrochloride (0.962 g, 6.56 mmol) and sodium hydrogen carbonate (0.551 g, 6.56 mmol) was stirred in N,N-dimethylformamide (10 mL) for 24 h at room temperature and then heated to 60° C. for 5 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 (683.7 mg) as an oil. Electrospray MS m/z 541 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218538B1
Source datasetuspto-grants-2001_04
ORD IDord-79bb35fc579442dabeebcc028bc7949b
Source noteuspto-grants-2001_04