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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551200Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 178427149, compound

https://huagongshe.com/reaction/551200

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178427148HCID 178427148—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 178427149HCID 178427149—

Reaction Conditions

Temperature-12.5 °C

Reaction Steps

204 mg (0.48 mmol) N-[(1S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethyl]-3-methyl-4-(thiomorpholin-3-on-4-yl)-benzamide are dissolved in a mixture of 12 ml dichloromethane and 1.2 ml acetic acid at −15° C. and combined with 110 mg (0.48 mmol) 3-chloroperbenzoic acid. The mixture is then stirred for one hour at −15 to −10° C., heated to ambient temperature and stirred for a further 3 hours. Then the reaction mixture is combined with semi-concentrated sodium hydrogen carbonate solution and extracted with a solvent mixture dichloromethane/methanol 19:1. The combined organic phases are washed with water, dried over magnesium sulphate, evaporated down i. vac. and purified by chromatography on silica gel (eluting gradient: ethyl acetate/(ethanol/conc. ammonia solution 19:1)=1:0→4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947700B2
Source datasetuspto-grants-2011_05
ORD IDord-b42e1b1f88f34dee84d73eeb881902fe
Source noteuspto-grants-2011_05