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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3168Generated: October 25, 2026

Methylamine → Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/3168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 29569781%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-chloro-2-methylsulfanyl-5-pyrimidinecarboxylate ethyl ester (18.66 g, 80.4 mmol) in 260 mL of tetrahydrofuran was added triethylamine (34 mL, 244 mmol), followed by 30 mL of a 40% aqueous solution of methylamine. The solution was stirred for 30 minutes at 25° C. then concentrated in vacuo and partitioned between chloroform and saturated aqueous sodium bicarbonate. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated to provide a white solid. The solid was suspended in hexane and filtered to provide 14.70 g (81%) of 4-methylamino-2-methylsulfanyl-5-pyrimidinecarboxylate ethyl ester; mp 91°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733914
Source datasetuspto-grants-1998_03
ORD IDord-dd5613fe644d4335b125576fcb33212e
Source noteuspto-grants-1998_03