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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514408Generated: November 5, 2026

Methanol → 2-Methanesulfonyl-5-methyl-4-pyridin-3-yl-pyrimidine

https://huagongshe.com/reaction/1514408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 59242786HCID 59242786—
Product2-Methanesulfonyl-5-methyl-4-pyridin-3-yl-pyrimidineHCID 6869731888%

Reaction Steps

A solution of 5-methyl-2-methylsulfanyl-4-pyridin-3-yl-pyrimidine (1.28 g, 5.90 mmol) in MeOH (45 ml) was cooled at 0° C. and then an aqueous solution of oxone (11 g, 17.95 mmol in 45 ml of water) was added dropwise. After 15 minutes, ice bath was removed and the stirring continue for 3 hours. The mixture was neutralized with solid NaHCO3 and the product was extracted with ethyl acetate. The organic phase was dried (Na2SO4) and evaporated to give 1.3 g of the title compound as a white powder (88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222266B2
Source datasetuspto-grants-2012_07
ORD IDord-f33826bba26143329662b10d8da64daa
Source noteuspto-grants-2012_07