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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612560Generated: November 4, 2026

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

https://huagongshe.com/reaction/1612560

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 numberUS05190575
Source datasetuspto-grants-1993_03
ORD IDord-496bb6ab2e39493e91634b6a6b7e520f
Source noteuspto-grants-1993_03