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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130486Generated: October 29, 2026

Pyridine → 1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanone

https://huagongshe.com/reaction/130486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantEthyl AcetateHCID 8857—
Reactant1-(2,3-Dihydro-1H-indol-5-yl)ethan-1-oneHCID 253117—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-ethanoneHCID 14112956—

Reaction Steps

1-(2,3-Dihydro-1H-indol-5-yl)-ethanone (0.200 g, 1.24 mmol) was dissolved in THF (2 ml) before pyridine (0.303 ml, 3.75 mmol) was added, leaving a yellow solution. The benzenesulfonyl chloride (0.220 g, 1.24 mmol) was then added, as a solid, with stirring. The reaction mixture was stirred at 40 C for 5 h. The mixture was cooled and the THF and pyridine were removed in vacuo. The desired sulfonamide (0.310 g, 1.02 mmol, 82%) was recrystallized from ethyl acetate and hexanes. It had LC-MS (ES+): 302 [MH]+ m/e

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381749B2
Source datasetuspto-grants-2008_06
ORD IDord-1a284aaa23ec4f8f9029bbecc9b61d57
Source noteuspto-grants-2008_06