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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814078Generated: October 25, 2026

Water → 2-(2-Tetrahydrofuranyl)-5-methanesulfonyl-1-benzenesulfonylindole

https://huagongshe.com/reaction/1814078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-EthynyloxolaneHCID 10034582—
Reactant1-Benzenesulfonylamino-2-iodo-4-methanesulfonylbenzeneHCID 22504376—
Solvent1,4-DioxaneHCID 31275—
Product2-(2-Tetrahydrofuranyl)-5-methanesulfonyl-1-benzenesulfonylindoleHCID 2250444991.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-benzenesulfonylamino-2-iodo-4-methanesulfonylbenzene (256 mg) in 1,4-dioxane (6 ml), 2-ethynyltetrahydrofuran (169 mg), bistriphenylphosphine palladium dichloride (21 mg), cuprous iodide (11 mg) and triethylamine (89 mg) were added successively and the mixture was stirred in a sealed tube at 60° C. for 3 hours. After cooling, the reaction solution was poured into water, extracted with dichloromethane, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) to obtain 218 mg of the desired product in a white amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-4dffaf6061d048778e2e6ae024b22aaf
Source noteuspto-grants-2005_04