Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36892Generated: October 23, 2026

Triethylamine → Vinyl 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carboxylate

https://huagongshe.com/en/reaction/36892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantVinyl chloroformateHCID 78808—
Reactant5-bromo-3-(piperidin-4-ylthio)-1H-indoleHCID 19936667—
SolventDichloromethaneHCID 6344—
ProductVinyl 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carboxylateHCID 19936620—

Reaction Steps

Vinyl chloroformate (0.75 ml) is added dropwise to a solution of triethylamine (1.2 ml) and 5-bromo-3-(piperidin-4-ylthio)-1H-indole (2.5 g, prepared in Example 49) in dichloromethane (25 ml) at 0° C. After 2 hours at room temperature, the solution is washed with water. The organic phase is dried over magnesium sulfate and concentrated. Vinyl 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carboxylate (1.8 g) is obtained after chromatography on silica gel (eluent: cyclohexane/AcOEt 70/30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418242
Source datasetuspto-grants-1995_05
ORD IDord-1b910d7bef7849f3b7e40343de7732e6
Source noteuspto-grants-1995_05