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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783313Generated: October 28, 2026

Isopropyl iodide → HCID 10423169, compound

https://huagongshe.com/reaction/1783313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10421246HCID 10421246—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 10423169HCID 10423169—

Reaction Conditions

Temperature40 °C

Reaction Steps

4-(1,2,3,6-Tetrahydropyridin-4-yl)-2H-isoquinolin-1-one (0.4 g) obtained in Example 205 and potassium carbonate (1 g) were suspended in acetonitrile (10 mL) and water (1 mL), and isopropyl iodide (0.35 mL) was added at room temperature. The mixture was stirred under heating overnight at 40° C. After the completion of the reaction, the solvent was evaporated. Aqueous potassium carbonate solution was added to the obtained residue, and the mixture was extracted with chloroform. The organic layer was dried over magnesium sulfate, and the solvent was evaporated. The obtained residue was subjected to silica gel column chromatography (NH silica gel, Fuji Silysia Chemical Ltd.). The fraction eluted with chloroform:methanol=25:1 was concentrated, and the precipitated crystals were collected by filtration to give 4-(1-isopropyl-1,2,3,6-tetrahydropyridin-4-yl)-2H-isoquinolin-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501412B2
Source datasetuspto-grants-2009_03
ORD IDord-2f29c37076ab4202b31983e93ade142b
Source noteuspto-grants-2009_03