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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615383Generated: November 4, 2026

m-Chloroperbenzoic acid → HCID 67204402, compound

https://huagongshe.com/reaction/1615383

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58159630HCID 58159630—
SolventDichloromethaneHCID 6344—
ProductHCID 67204402HCID 67204402107.4%

Reaction Steps

1-(2-(Methylthio)pyrimidin-4-yl)-6-(3-nitrophenyl)-1H-indole (91 mg, 0.251 mmol) was dissolved in methylene chloride (1 mL). At 0° C., 3-chloroperoxybenzoic acid (87 mg, 0.502 mmol) was added. 1 hour later, the reaction mixture was added to sodium bicarbonate aqueous solution and extracted with methylene chloride. The combined organic layer was washed with brine, dried with magnesium sulfate, and concentrated under reduced pressure. 1-(2-(Methylsulfinyl)pyrimidin-4-yl)-6-(3-nitrophenyl)-1H-indole (102 mg) was yielded.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765749B2
Source datasetuspto-grants-2014_07
ORD IDord-97186357d5594aaeb8a25617147e62cd
Source noteuspto-grants-2014_07