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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871883Generated: October 30, 2026

Aniline → Ethyl 2-(methylthio)-4-(phenylamino)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/871883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(methylthio)-4-(phenylamino)pyrimidine-5-carboxylateHCID 29567264.2%

Reaction Steps

To a solution of 5.0 g (21.49 mmol) of ethyl 4-chloro-2-methylsulfanyl-5-pyrimidinecarboxylate and 4.9 mL (53.72 mmol) of aniline in 75 mL of THF are added 7.49 mL (53.72 mmol) of triethylamine. The mixture is stirred at room temperature overnight. After evaporating off the THF, aqueous 1N HCl solution is added and the mixture is extracted with ethyl acetate. The organic phase is washed with saturated aqueous NaHCO3 solution and then with NaCl solution. The organic phase is dried over MgSO4. After filtering, the filtrate is concentrated to give 3.99 g of the expected product in the form of a beige-coloured solid, which is used as obtained in the following step. Yield=64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975250B2
Source datasetuspto-grants-2015_03
ORD IDord-dad508be5f3649d5b1b2e48d2048aa18
Source noteuspto-grants-2015_03