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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847509Generated: October 31, 2026

Methyl iodide → HCID 9994544, compound

https://huagongshe.com/reaction/847509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178421668HCID 178421668—
SolventDimethylformamideHCID 6228—
ProductHCID 9994544HCID 999454427.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 8,9-dihydro-7-[(1H-imidazol-4-yl)-methyl]-10-methylpyrido[1,2-a]indol-6(7H)-one (1.4 g) in N,N-dimethylformamide (14 ml) at 5° C. was added sodium hydride (60% in mineral oil) (220 mg). After stirring for 1 hour at 5° C, methyl iodide (852 mg) in dimethylformamide (5 ml) was added dropwise at 5° C. for 10 minutes. The mixture was stirred at 5° C. for 1 hour and at 20° C. for 2 hours. After evaporation of the solvent, the residue was diluted with 5% methanol-chloroform. The organic layer was washed twice with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The obtained residue contained two products which showed close Rf values (0.5 and 0.4 respectively) by TLC (20% methanol-chloroform). Separation with silica gel column chromatography (5% methanol-chloroform) gave two fractions. The first eluted fraction, containing a mixture of two products, was concentrated. The crystalline residue was recrystallized from ethyl acetate to give 8,9-dihydro-10-methyl-7-[(1-methyl-1H-imidazol-4-yl)methyl]pyrido[1,2-a]indol-6(7H)-one (0.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05141945
Source datasetuspto-grants-1992_08
ORD IDord-e9e9159024194cd6837c5d1018769482
Source noteuspto-grants-1992_08