Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435358Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 21070559, compound

https://huagongshe.com/reaction/1435358

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 21070576HCID 21070576—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 21070559HCID 21070559—

Reaction Steps

A solution of (4-amino-2-ethylsulfanyl-pyrimidin-5-yl)-(2-methoxy-5-methyl-phenyl)-methanone, 571 mg, 1.885 mmol, Example 324) in chloroform (16 mL) was cooled to −15° C. and treated with 3-chloroperoxybenzoic acid (503.7 mg, ˜2.25 mmol, ˜70% purity from Aldrich) and the reaction was stirred at the same temperature for 1 hour. The reaction mixture was diluted with methylene chloride (20 mL) and washed with 10% aqueous sodium thiosulfate (2×5 mL), 10% aqueous sodium carbonate (2×5 mL), brine, dried and concentrated to give (4-amino-2-ethanesulfinyl-pyrimidin-5-yl)-(2-methoxy-5-methyl-phenyl)-methanone as a white solid. MS (M+H)+: 320.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615634B2
Source datasetuspto-grants-2009_11
ORD IDord-5b25b19f0ecf4689bf69d2053b5a8874
Source noteuspto-grants-2009_11