Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375506Generated: October 25, 2026

4-Amidinobenzamide Hydrochloride → 4-[5-(4-Cyanophenyl)-2-pyrimidinyl]benzamide

https://huagongshe.com/reaction/375506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amidinobenzamide HydrochlorideHCID 2724293—
ReactantSodiumHCID 5360545—
Reactant2-(4-Cyanophenyl)-3-methoxyacroleinHCID 54100265—
SolventMethanolHCID 887—
Product4-[5-(4-Cyanophenyl)-2-pyrimidinyl]benzamideHCID 18991914—

Reaction Steps

247 mg of sodium are treated at room temperature with 10 ml of methanol. After 15 minutes the solution obtained is treated at room temperature with 1.58 g of 4-amidinobenzamide hydrochloride. A white suspension forms and this is treated dropwise at room temperature within 10 minutes with a solution of 1.42 g of 2-(4-cyanophenyl)-3-methoxyacrolein in 50 ml of methanol. The reaction mixture is stirred at room temperature for a further 2 hours and then suction filtered. The residue is washed with water, tetrahydrofuran and diethyl ether and dried in a high vacuum. 4-[5-(4-Cyanophenyl)-2-pyrimidinyl]benzamide is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486310
Source datasetuspto-grants-1996_01
ORD IDord-f2c4875e63134ec497c2dfd574b7b513
Source noteuspto-grants-1996_01