Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548635Generated: October 29, 2026

Potassium Iodide → HCID 16663103, compound

https://huagongshe.com/reaction/548635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantHCID 16058746HCID 16058746—
SolventAcetonitrileHCID 6342—
ProductHCID 16663103HCID 1666310342%

Reaction Conditions

Temperature50 °C

Reaction Steps

(Bromomethyl)cyclopropane a48 (47 μl, 0.48 mmol, 2.1 eq) is added to a solution of (5S)-5-{[(cyclohexylmethyl)amino]methyl}-1-[4-(3-piperidin-1-ylpropoxy)phenyl]pyrrolidin-2-one 2 in acetonitrile (4 ml), then cesium carbonate (150 mg, 0.46 mmol, 2 eq) and potassium iodide (8 mg, 0.05 mmol, 0.2 eq) are added and the mixture is heated at 50° C. for 24 h. The precipitate is filtered and the solvent is removed in vacuo. The residue is dissolved into dichloromethane and washed with a saturated solution of aqueous ammonium chloride. The aqueous layer is then extracted with dichloromethane, the organic layers are dried over magnesium sulfate and concentrated in vacuo to give 109 mg of a yellow oil. This oil is purified by chromatography over silicagel (dichloromethane/methanol/ammonia 92/8/0.8) to obtain 47 mg of (5S)-5-{[(cyclohexylmethyl)(cyclopropylmethyl)amino]methyl}-1-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}pyrrolidin-2-one 3 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943605B2
Source datasetuspto-grants-2011_05
ORD IDord-3f5401e139bf4d468fb5aaa9b950ba89
Source noteuspto-grants-2011_05