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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012304Generated: October 31, 2026

HCID 23152475, compound → HCID 23152479, compound

https://huagongshe.com/reaction/1012304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23152475HCID 23152475—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23152479HCID 2315247987.1%

Reaction Steps

A suspension of N-tert-butyl-4-((E)-2-dimethylaminovinyl)-3-nitrobenzenesulfonamide (5.41 g, 16.5 mmol) and 7.5% palladium/carbon (500 mg) in tetrahydrofuran (50 ml) and ethanol (50 ml) was stirred at room temperature for 3.5 hr under a hydrogen atmosphere of 3.5 atm. The reaction mixture was filtered through celite and the filtrate was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was successively washed with 1N hydrochloric acid and saturated brine and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure to give N-tert-butyl-1H-indole-6-sulfonamide (3.62 g, yield 87.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-a131108c3af247bfbd2fe4a545cc370c
Source noteuspto-grants-2011_07