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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284708Generated: October 29, 2026

Hydrochloric Acid → 2-((3-Fluorophenyl)amino)-4-(propylamino)pyrimidine-5-carboxylic acid

https://huagongshe.com/reaction/2284708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 90052261HCID 90052261—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product2-((3-Fluorophenyl)amino)-4-(propylamino)pyrimidine-5-carboxylic acidHCID 9005211757.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl 2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidine-5-carboxylate (E3, 247 mg) in ethanol (3 mL) and tetrahydrofuran (1.5 mL), 2.0 mol/L aqueous sodium hydroxide (0.78 mL) was added at room temperature, and the mixture was stirred at 50° C. for 1 hour. To the reaction mixture, 2.0 mol/L aqueous sodium hydroxide (0.39 mL) was added at 50° C., and the mixture was stirred at the same temperature for 3 hours. The reaction mixture was cooled to room temperature, and then 1.0 mol/L aqueous hydrochloric acid was added to the reaction mixture until the mixture became acidic. The solid matter was taken by filtration, washed with water, and then dried under reduced pressure to obtain 2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidine-5-carboxylic acid (E22, 130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-dd507d80924b4c28b97841d28f0ca52f
Source noteuspto-grants-2015_09