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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947035Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 69309553, compound

https://huagongshe.com/reaction/1947035

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 69307229HCID 69307229—
SolventChloroformHCID 6212—
ProductHCID 69309553HCID 6930955392.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-ethyl-N-[1-(2-methylsulfanyl-pyrimidin-4-yl)-1H-indol-4-yl]-methanesulfonamide (0.4 g) in CHCl3 (60 mL) was cooled to 0° C. and MCPBA (0.247 g) added and stirred at 0° C. for 5 h before quenching with 10% sodium thiosulfate solution. The organic layer was separated, dried over sodium sulfate, filtered, concentrated and purified on a column using 100% DCM to 15% MeOH/DCM to yield N-ethyl-N-[1-(2-methylsulfinyl-pyrimidin-4-yl)-1H-indol-4-yl]-methanesulfonamide (0.386 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399462B2
Source datasetuspto-grants-2013_03
ORD IDord-deca4d7fa4674e068be8c1189a7efa21
Source noteuspto-grants-2013_03