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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326812Generated: October 31, 2026

Methanesulfonyl chloride → 2-(4-Fluorophenyl)-4-(3-methanesulfonyloxyphenyl)-5-methoxypyrimidine

https://huagongshe.com/reaction/326812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 14883712HCID 14883712—
SolventPyridineHCID 1049—
Product2-(4-Fluorophenyl)-4-(3-methanesulfonyloxyphenyl)-5-methoxypyrimidineHCID 1488375766%

Reaction Steps

1.2 g of 2-(4-fluorophenyl)-4-(3-hydroxyphenyl)-5-methoxypyrimidine and 0.57 g of methanesulfonyl chloride were added to 10 ml of pyridine, and the resulting mixture was stirred for 3 hours at room temperature. After completion of the reaction, ice-cold water was added to the mixture. Subsequently, the mixture was extracted with ethyl acetate. The solvent was evaporated off, and the residue was purified by column chromatography on silica gel, thereby obtaining 1.0 g 2-(4-fluorophenyl)-4-(3-methanesulfonyloxyphenyl)-5-methoxypyrimidine (Compound 54).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270467
Source datasetuspto-grants-1993_12
ORD IDord-d096bf354e3e4377853f7b953a78467c
Source noteuspto-grants-1993_12