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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286231Generated: October 30, 2026

Dimethylformamide → HCID 13002707, compound

https://huagongshe.com/reaction/2286231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
Reactant3-(3-Bromopropyl)-2-methyl-1H-indoleHCID 13002706—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 13002707HCID 13002707—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-(3-bromopropyl)-2-methylindole (13.8 g), 4-(4-fluorobenzoyl)piperidine (6.0 g), K2CO3 (4.0 g) and dimethylformamide (DMF) (100 ml) is stirred and heated at 50° C. under N2 for 16 hours. The mixture is poured into H2O, and the aqueous mixture extracted with benzene, the benzene extract is washed with H2O, dried (Na2SO4), and the solvent evaporated to leave an oil. The oil is taken up in ether and HCl (g) is bubbled into it to precipitate 10.6 g of a hydrochloride salt. The salt is converted to the free base (an oil). Upon trituration of the oil with ether 4.2 g of a solid is collected. The solid is recrystallized from EtOH-H2O (charcoal treatment), and then twice from isopropanol to yield 1.9 g (15%), m.p. 135°-137° of 3-{3-[4-(4-fluorobenzoyl)piperidyl]propyl} 2-methylindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04327103
Source datasetuspto-grants-1982_04
ORD IDord-ad5c930285a8432bb4a8ebaa0d70d75b
Source noteuspto-grants-1982_04