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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007840Generated: October 31, 2026

Citric Acid → Ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylsulfanyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1007840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
Reactant3-Chloro-4-methoxybenzylamineHCID 738038—
Catalyst3-Chloro-4-methoxybenzylamineHCID 738038—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductEthyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 2202592795.7%

Reaction Steps

To a solution of 4-chloro-5-ethoxycarbonyl-2-methylthio-pyrimidine (25.33 g) in N,N-dimethylformamide (85 ml) are added a solution of 3-chloro-4-methoxybenzylamine (19.62 g) in N,N-dimethyl-formamide (15 ml) and triethylamine (16.7 ml) under ice-cooling. The mixture is stirred at room temperature for 20 minutes, and thereto is added 3-chloro-4-methoxybenzylamine (940 mg), and the mixture is further stirred for 15 minutes. To the mixture is further added said amine (940 mg), and the mixture is stirred for 15 minutes. The reaction mixture is poured into a mixture of ice water and citric acid, and the mixture is extracted with ethyl acetate. The extract is washed successively with a 10% aqueous citric acid solution, water and brine, and dried over anhydrous sodium sulfate. The solvent is evaporated under reduced pressure, and the residue is washed with n-hexane to give 4-(3-chloro-4-methoxybenzylamino)-5-ethoxycarbonyl-2-methylthiopyrimidine (38.34 g), m.p. 86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797709B2
Source datasetuspto-grants-2004_09
ORD IDord-db988d2226394e789952f0019a61bc44
Source noteuspto-grants-2004_09