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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209997Generated: October 30, 2026

Potassium Iodide → HCID 54135875, compound

https://huagongshe.com/reaction/2209997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
ReactantHCID 10339222HCID 10339222—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54135875HCID 54135875—

Reaction Steps

To a solution of 3-[1-(2-aminoethyl)-4-piperidyl]-6-chloro-1-(4-fluorophenyl)-1H-indole 7b (11 g)in dioxan (100 ml) were added 2-bromo-1,1-dimethoxyethane (5.6 g), potassium carbonate (5 g) and a potassium iodide crystal. The mixture was refluxed for 16 hours. After cooling inorganic salts were filtered off and dioxan evaporated leaving crude 6-chloro-3-[1-[N-(1,1-dimethoxyethyl)-aminoethyl]-4-piperidyl]-1-(4-fluorophenyl)-1H-indole as an oil. The crude product was purified by column chromatography on silica gel (eluted with ethyl acetate/methanol 1:1). Yield: 6 g as an oil. The thus obtained alkylated aminoderivative (6 g) was dissolved in dichloromethane (100 ml) and 2-propylisocyanate (1.1 g) was added. After refluxing for 2 hours dichloromethane was evaporated and the title compound 16a was purified by column chromatography on silica gel (eluted with ethyl acetate/methanol 1:1). Yield: 4.9 g as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457115
Source datasetuspto-grants-1995_10
ORD IDord-9f2c70b82cce471f9f1cd6512f35b976
Source noteuspto-grants-1995_10