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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378365Generated: October 29, 2026

Triethylamine → Methyl 3-phenoxy-3-phenyl-2-[(4,6-dimethoxy-2-pyrimidinyl)thio]butyrate

https://huagongshe.com/reaction/378365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-benzyloxy-3-phenyl-2-hydroxybutyrateHCID 15292268—
ReactantHCID 178493561HCID 178493561—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-phenoxy-3-phenyl-2-[(4,6-dimethoxy-2-pyrimidinyl)thio]butyrateHCID 1529230038.1%

Reaction Steps

7.2 g (25 mmol) of methyl 3-phenoxy-3-phenyl-2-hydroxybutyrate (Compound 1.1) are dissolved in 50 ml of dichloromethane, 3 g (30 mmol) of triethylamine are added and, while stirring, 3.2 g (28 mmol) of methanesulfonyl chloride are added dropwise. The mixture is stirred at room temperature for 2 hours, washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue is taken up in 100 mo of DMF and added dropwise to a suspension 12.9 g (75 mmol) of 4,6-dimethoxypyrimidine-2-thiol and 8.4 g (100 mmol) sodium bicarbonate in 100 ml of DMF at 0° C. After stirring at room temperature for 2 hours and at 60° C. for further 2 hours, the mixture is poured into 1 liter of ice-water, and the precipitate is filtered off with suction. Drying results in 4.2 g of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030975
Source datasetuspto-grants-2000_02
ORD IDord-51f43ff620c64095b90bfe1cffaab82a
Source noteuspto-grants-2000_02