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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745009Generated: October 30, 2026

Triethylamine → (R)-5-(2-Ethylsulphonylethenyl)-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole

https://huagongshe.com/reaction/745009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Ethylsulfonyl)etheneHCID 74680—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant(R)-5-Bromo-3-(1-methyl-2-pyrrolidinyl methyl)-1H-indoleHCID 11185464—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product(R)-5-(2-Ethylsulphonylethenyl)-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indoleHCID 5450432065.3%

Reaction Steps

A mixture of (R)-5-bromo-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole (0.25 g), ethyl vinyl sulphone (0.14 g), tri-o-tolylphosphine (0.075 g), palladium (II) acetate (0.013 g), triethylamine (0.25 mL) and acetonitrile (3 mL) was heated under reflux for 17 hours in an atmosphere of nitrogen. The mixture was evaporated and the residue was chromatographed on silica gel. Elution with dichloromethane/ethanol/concentrated aqueous ammonia (90:8:1) gave the title compound as a foam (0.185 g): TLC (dichloromethane/-ethanol/concentrated aqueous ammonia, 90:10:1): Rf =0.5. Anal. Calcd for C18H24N2O2S. 0.2 CH2Cl2 : C,62.55; H,7.04; N,8.02. Found: C,62.65; H,6.94; N,7.92.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559246
Source datasetuspto-grants-1996_09
ORD IDord-6a1fbe1efffc40c696e446c9dd3ccb52
Source noteuspto-grants-1996_09