Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769259Generated: October 27, 2026

Acetic Acid → n-Propyl 2-amino-1,4-dihydro-5-cyano-6-methyl-4-(3-phenylquinolin-5-yl)-pyridine-3-carboxylate

https://huagongshe.com/reaction/1769259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant5-MethylisoxazoleHCID 79833—
ReactantSodiumHCID 5360545—
ReactantPropyl amidinoacetate hydrochlorideHCID 12391079—
Reactant3-Phenylquinoline-5-carbaldehydeHCID 15170332—
Solvent1-PropanolHCID 1031—
Productn-Propyl 2-amino-1,4-dihydro-5-cyano-6-methyl-4-(3-phenylquinolin-5-yl)-pyridine-3-carboxylateHCID 6778061216.3%

Reaction Steps

23.3 g (100 mmol) of 3-phenyl-quinoline-5-aldehyde are suspended in 200 ml of n-propanol and the suspension is stirred with 8.25 ml (100 mmol) of 5-methylisoxazole. A solution of 2.3 g of sodium in 100 ml of n-propanol is added dropwise and the mixture is stirred at 40°-50° C. for 4 hours. A brown solution is obtained by this procedure. 18.04 g (100 mmol) of propyl amidinoacetate hydrochloride and 6 ml of acetic acid (100 mmol) are added and the mixture is boiled for 20 hours. It is concentrated, the residue is dissolved in ethyl acetate/water and the phases are separated. The ethyl acetate phase is washed with sodium bicarbonate solution and twice with water, dried and concentrated. The resulting residue is dissolved in 100 ml of hot acetonitrile and the product is left to crystallise. It is filtered off with suction and recrystallised from n-propanol and then from acetonitrile. 6.9 g of colourless crystals of melting point 237° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380851
Source datasetuspto-grants-1995_01
ORD IDord-3b6bdef469e2473ea9aa32ec1c78b1c6
Source noteuspto-grants-1995_01