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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790459Generated: October 31, 2026

Isopropylamine → 1-[1-(4-Fluorophenethyl)-piperdin-4-yl]-6-(isopropylcarbamoylmethyl)indoline

https://huagongshe.com/reaction/1790459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantEthyl AcetateHCID 8857—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-carboxymethylindolineHCID 22038043—
SolventDimethylformamideHCID 6228—
Product1-[1-(4-Fluorophenethyl)-piperdin-4-yl]-6-(isopropylcarbamoylmethyl)indolineHCID 2203797452%

Reaction Steps

Under ice cooling, 1,1′-carbonyldimidazole (15 g) was added to a solution of 1-[1-(4-fluorophenethyl)piperidin-4-yl]-6-carboxymethylindoline (30 g) in dimethylformamide (240 ml) and the resultant mixture was stirred for 2 hr. After adding isopropylamine (5.6 g), the mixture was warmed to room temperature and then stirred for additional 2 hr. Next, ice water (240 ml) and ethyl acetate (300 ml) were added to the reaction solution and the layers were separated. The organic layer was washed successively with water, a saturated aqueous solution of sodium bicarbonate and brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in hot ethyl acetate (80 ml). After allowing to cool to room temperature, the resulting crystals were collected by filtration to give the title compound (17.2 g) as a white powder (yield: 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-1cb140fd327d45739df3badf916eff95
Source noteuspto-grants-2006_07