Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159808Generated: October 27, 2026

Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-4-pyrazin-2-yl-1H-indole

https://huagongshe.com/reaction/1159808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant4-pyrazin-2-yl-1H-indoleHCID 68717665—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(Phenylsulfonyl)-4-pyrazin-2-yl-1H-indoleHCID 68717002—

Reaction Steps

4-Pyrazin-2-yl-1H-indole (0.060 g, 0.307 mmol, Intermediate 65), benzensulfonyl chloride (0.071 g, 0.40 mmol) and tetrabutylammonium hydrogen sulfate (0.010 g, 0.031 mmol) were dissolved in dichloromethane (3 mL) and NaOH (0.061 g, 1.5 mmol) in water (1 mL) was added. The mixture was stirred at rt overnight and the mixture was diluted with dichloromethane and water and extracted with dichloromethane (2×). The organic phase was dried (MgSO4) and evaporated. The crude product was purified by flash chromatography using CH2Cl2 to 1% MeOH in CH2Cl2 as the eluent. Yield: 81 mg (79%). White solid. MS (electronspray; [M+H]+) m/z 336.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-87b331da22134b10804f6b12ed049ebd
Source noteuspto-grants-2010_10