HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548635Generated: October 29, 2026
Potassium Iodide → HCID 16663103, compound
https://huagongshe.com/reaction/548635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | HCID 16058746 | HCID 16058746 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 16663103 | HCID 16663103 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943605B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-3f5401e139bf4d468fb5aaa9b950ba89 |
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| Source note | uspto-grants-2011_05 |
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