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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279384Generated: October 31, 2026

1-(Benzenesulfonyl)-5-bromo-1H-indole → 1-Benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole

https://huagongshe.com/reaction/1279384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzenesulfonyl)-5-bromo-1H-indoleHCID 2776210—
Reactant1-(3-Butynyl)-4-benzylpiperidineHCID 10609355—
CatalystHCID 178418397HCID 178418397—
SolventPyrrolidineHCID 31268—
Product1-Benzenesulfonyl-5-[4-(4-benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indoleHCID 1842795680.3%

Reaction Steps

A mixture of 1-benzenesulfonyl-5-bromoindole (1.34 g, 4 mmol), 4-benzyl-1-(3-butynyl)-piperidine (908 mg, 4 mmol) and tetrakis(triphenylphosphine)palladium (0) (600 mg) is stirred in pyrrolidine (50 mL) at 50° C. under N2 overnight. Most of the pyrrolidine is evaporated and the residue purified by medium-pressure column chromatography on silica gel eluting with 50% increasing to 100% EtOAc/hexanes to give the title compound as a pale yellow oil (1.55 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448270B1
Source datasetuspto-grants-2002_09
ORD IDord-7997806fe34f44889798bd0d3a89202b
Source noteuspto-grants-2002_09