Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403181Generated: October 26, 2026

Methanol → 5-Fluoro-2-(methylsulfonyl)pyrimidin-4-amine

https://huagongshe.com/reaction/1403181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Fluoro-2-(methylthio)pyrimidin-4-amineHCID 20593351—
ReactantSodium BisulfiteHCID 23665763—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
Product5-Fluoro-2-(methylsulfonyl)pyrimidin-4-amineHCID 5831893463%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 5-fluoro-2-methylsulfanylpyrimidin-4-ylamine (5.02 g, 31.6 mmol) in methyl alcohol (MeOH; 105 mL) was added dropwise a solution of OXONE™ (Registered trademark of E.I. du Pont de Nemours & Co, Inc.; 42.7 g, 69.4 mmol) in H2O (210 mL) over a 20 minute (min) period at −45° C., and the resulting mixture was slowly warmed to 10° C. over a period of 14 h. The mixture was treated with sodium bisulfite (10 g) and the majority of the MeOH was removed on the rotary evaporator. The aqueous residue was extracted with EtOAc (2×250 mL), and the organic extracts were combined, washed with brine (100 mL), dried over Na2SO4, filtered, and concentrated to give 5-fluoro-2-methanesulfonylpyrimidin-4-ylamine (3.79 g, 63%) as a white solid: mp 157-159° C.; 1H NMR (300 MHz, DMSO-d6) δ 8.35 (d, J=3.6 Hz, 1H), 8.11 (s, 2H), 3.27 (s, 3H); CIMS m/z 191 ([M]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912207B2
Source datasetuspto-grants-2014_12
ORD IDord-e2468e004a5b4b2a94afdb7b64a0ccfd
Source noteuspto-grants-2014_12