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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284651Generated: November 1, 2026

Hydrochloric Acid → 2-((4-Carbamoylphenyl)amino)-4-(propylamino)pyrimidine-5-carboxylic acid

https://huagongshe.com/reaction/2284651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-((4-carbamoylphenyl)amino)-4-(propylamino)pyrimidine-5-carboxylateHCID 90051724—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product2-((4-Carbamoylphenyl)amino)-4-(propylamino)pyrimidine-5-carboxylic acidHCID 9005172554.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 2-((4-carbamoylphenyl)amino)-4-(propylamino)pyrimidine-5-carboxylate (C1, 8.0 g) in tetrahydrofuran (240 mL) and methanol (240 mL), water (40 mL) and 5.0 mol/L aqueous sodium hydroxide (48 mL) were added at room temperature, and the mixture was stirred at 60° C. for 3 hours. The reaction mixture was cooled on ice, then 12 mol/L aqueous hydrochloric acid was added to the mixture until pH of the mixture became 2, and the reaction mixture was poured into ice water (2000 mL). The solid matter was taken by filtration, washed with water, and then dried under reduced pressure to obtain 2-((4-carbamoylphenyl)amino)-4-(propylamino)pyrimidine-5-carboxylic acid (C2, 4.0 g) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-69d8e2859dae42fea4ad7417426c3b76
Source noteuspto-grants-2015_09