Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657363Generated: November 3, 2026

Potassium Carbonate → 9-[(2-Bromo-4-chlorobenzyl)oxy]-4-oxo-4H-pyrido [1,2-alpha]pyrimidine-3-carboxylic Acid, Ethyl Ester

https://huagongshe.com/reaction/1657363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylateHCID 616445—
Reactant2-Bromo-1-(bromomethyl)-4-chlorobenzeneHCID 10613066—
SolventMethyl Ethyl KetoneHCID 6569—
Product9-[(2-Bromo-4-chlorobenzyl)oxy]-4-oxo-4H-pyrido [1,2-alpha]pyrimidine-3-carboxylic Acid, Ethyl EsterHCID 131710255108.2%

Reaction Steps

To 4.7 g of 9-hydroxy-4-oxo-4H-pyrido[1,2-α]pyrimidine-3-carboxylic acid, ethyl ester, 7.2 g of 2-bromo-4-chlorobenzyl bromide and 200 ml of ethyl methyl ketone is added 3.3 g of anhydrous potassium carbonate. The mixture is stirred and heated under reflux for 18 hours, cooled and filtered. The filtrate is concentrated in vacuo to give 9.5 g of a viscous gum. This is dissolved in 100 ml of chloroform and the chloroform solution is washed with 60 ml of 5% aqueous potassium hydroxide. The chloroform solution is separated, washed with 25 ml of saturated aqueous sodium chloride, dried, and concentrated to give 7.4 g of a viscous gum. This gum is crystallized in 250 ml of 1:1 toluene-Skellysolve E to give 3.6 g of green crystals that sinter at 155° and melt at 162°-165°. A second recrystallization from 225 ml of 2-propanol gives the yellow crystalline named product, m.p. about 167°-169°. The yield is about 2.95 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03960847
Source datasetuspto-grants-1976_06
ORD IDord-75294a8ca3e6409bb55b46a17c3cfa07
Source noteuspto-grants-1976_06