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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790474Generated: October 31, 2026

Chlorosuccinimide → HCID 22038099, compound

https://huagongshe.com/reaction/1790474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 22037919HCID 22037919—
SolventAcetonitrileHCID 6342—
ProductHCID 22038099HCID 2203809934.5%

Reaction Steps

N-Chlorosuccinimide (0.24 g) was added at room temperature to a solution of 1-[1-(4-fluorophenethyl)piperidin-4-yl]-6-aminoindoline (0.5 g) in acetonitrile (50 ml) and the resultant mixture was stirred for 1 hr. Then the reaction mixture was filtered and concentrated under reduced pressure. Next, a 5 N aqueous solution of sodium hydroxide and ethyl acetate were added thereto and the layers were separated. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The resulting residue was purified by silica gel column chromatography (methylene chloride/ethanol system) to give the title compound (0.19 g) as a brown oil (yield: 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-91568a1f09ec49e28d81837910dbdcf9
Source noteuspto-grants-2006_07