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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284698Generated: October 30, 2026

4-Aminopyridine → Ethyl 4-(propylamino)-2-(3-(pyridin-4-yl)ureido)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/2284698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantDimethylformamideHCID 6228—
ReactantEthyl 2-((phenoxycarbonyl)amino)-4-(propylamino)pyrimidine-5-carboxylateHCID 90052190—
SolventWaterHCID 962—
ProductEthyl 4-(propylamino)-2-(3-(pyridin-4-yl)ureido)pyrimidine-5-carboxylateHCID 9005331428.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

To ethyl 2-((phenoxycarbonyl)amino)-4-(propylamino)pyrimidine-5-carboxylate (E7, 2.89 g) and 4-aminopyridine (3.16 g), N,N-dimethylformamide (30 mL) was added at room temperature, and the mixture was stirred at 70° C. for 30 minutes. The reaction mixture was cooled to room temperature, and then the reaction mixture was poured into water (300 mL). The solid matter was taken by filtration, and purified by silica gel column chromatography (eluent, ethyl acetate) to obtain ethyl 4-(propylamino)-2-(3-(pyridin-4-yl)ureido)pyrimidine-5-carboxylate (E8, 830 mg) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-81994395a7104e35a615ea6d15c1e6d5
Source noteuspto-grants-2015_09