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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432213Generated: October 30, 2026

Water → 1-Benzenesulfonyl-5-methanesulfonyl-2-([1,3,4]oxadiazol-2-yl)indole

https://huagongshe.com/reaction/1432213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant1-benzenesulfonyl-5-methylthio-2-([1,3,4]oxadiazol-2-yl)-1H-indoleHCID 22504401—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Product1-Benzenesulfonyl-5-methanesulfonyl-2-([1,3,4]oxadiazol-2-yl)indoleHCID 22504426—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the compound obtained in Example 4 (1) (265 mg) in tetrahydrofuran (7 ml), an aqueous solution (3.5 ml) of OXONE (registered trademark) (970 mg) was added dropwise and the mixture was stirred at 0° C. for 4 hours. To the reaction solution was added water, the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 262 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612070B2
Source datasetuspto-grants-2009_11
ORD IDord-ed58eca8cd434059bcc0c0475e105962
Source noteuspto-grants-2009_11