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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356867Generated: October 30, 2026

Triethylamine → Methyl 3-benzyloxy-3-phenyl-2-(4,6-dimethoxypyrimidin-2-ylthio)-butyrate

https://huagongshe.com/reaction/356867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 3-benzyloxy-3-phenyl-2-hydroxybutyrateHCID 15292268—
ReactantSodium dimethylformamideHCID 86746767—
ReactantHCID 178493561HCID 178493561—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-benzyloxy-3-phenyl-2-(4,6-dimethoxypyrimidin-2-ylthio)-butyrateHCID 1529227529%

Reaction Steps

11 g (25 mmol) of methyl 3-benzyloxy-3-phenyl-2-hydroxybutyrate (comp. 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 DMF and added dropwise to a suspension of 12.9 g (75 mmol) of 4,6-dimethoxypyrimidine-2-thiol and 8.4 g (100 nmol) of sodium DMF at 0° C. After stirring at room temperature for 2 hours and at 60° C. for a further 2 hours, the mixture is poured into 1 1 of ice-water, and the precipitate is filtered off with suction. Drying results in 3.2 g of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840722
Source datasetuspto-grants-1998_11
ORD IDord-3cfcf8f88c6248a289a5131a0e00c216
Source noteuspto-grants-1998_11