Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348435Generated: October 26, 2026

m-Chloroperbenzoic acid → 2-Methanesulfinylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide

https://huagongshe.com/reaction/348435

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-(4-fluorophenyl)-2-(methylthio)-5-pyrimidinecarboxamideHCID 58802987—
SolventDichloromethaneHCID 6344—
SolventMethylenechloride HexaneHCID 21226440—
Product2-Methanesulfinylpyrimidine-5-carboxylic acid (4-fluorophenyl)amideHCID 8676038473.4%

Reaction Steps

To a solution of 2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide (2.00 g, 7.60 mmol) in dichloromethane (76 mL) was added m-CPBA (67%, 2.02 g, 7.84 mmol) in one portion. Solid precipitate appeared within 2 min, and after 10 min the solution was diluted with 2/1 dichloromethane/hexane (60 mL). The solids were collected by filtration and washed with 50% dichloromethane/hexane to afford, after drying, 1.558 g (73% yield) of the titled sulfoxide. A second crop was obtained by concentrating the filtrate and triturating the solids first with hot 2/1 dichloromethane/hexane, and then after filtration by a second trituration with acetone. An additional 0.22 g (10%) of titled product was obtained, and was shown by 1H NMR to be contaminated with 10% sulfone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176310B1
Source datasetuspto-grants-2007_02
ORD IDord-df9c7ac5308a49a8aff0716f4f50424b
Source noteuspto-grants-2007_02