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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372998Generated: October 26, 2026

Triethylamine → 7-(2-Ethoxycarbonylethylamino)-4-oxo-2-(2-propoxyphenyl)3,4-dihydropyrimido[4,5-d]pyrimidine

https://huagongshe.com/reaction/372998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactant7-Methylsulphonyl-4-oxo-2-(2-propoxyphenyl)-3,4-dihydropyrimido[4,5-d]pyrimidineHCID 135670752—
SolventDichloromethaneHCID 6344—
Product7-(2-Ethoxycarbonylethylamino)-4-oxo-2-(2-propoxyphenyl)3,4-dihydropyrimido[4,5-d]pyrimidineHCID 135670771—

Reaction Steps

A solution of 7-methylsulphonyl-4-oxo-2-(2-propoxyphenyl)-3,4-dihydropyrimido[4,5-d]pyrimidine (1.0 g), β-alanine ethyl ester hydrochloride (1.10 g) and triethylamine (0.73 g) in dichloromethane (20 ml) was stirred at ambient temperature for 2.5 hours. The reaction mixture was extracted with dilute hydrochloric acid (20 ml) then water (10 ml), and the extracts back washed with dichloromethane (10 ml). The combined organic extracts were dried (magnesium sulphate) and evaporated under reduced pressure to yield a crude product which was recrystallised from ethanol: water to yield the title compound, 0.83 g, m.p. 142°-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162316
Source datasetuspto-grants-1992_11
ORD IDord-e5ef1ee8fa57457580765a4dcf39d892
Source noteuspto-grants-1992_11