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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399052Generated: October 30, 2026

Methyl iodide → 9-Chloro-1-(2,4-dichlorophenyl)-6-(1-methoxypropyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole

https://huagongshe.com/reaction/1399052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 44156374HCID 44156374—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
Product9-Chloro-1-(2,4-dichlorophenyl)-6-(1-methoxypropyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazoleHCID 5778631276.3%

Reaction Steps

A mixture of 1-[9-chloro-1-(2,4-dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl]propan-1-ol (460 mg, 1.12 mmol), potassium carbonate (201 mg, 1.46 mmol) and methyl iodide (207 mg, 1.46 mmol) in N,N-dimethylformamide (4.5 mL) was stirred at room temperature for 9 hr. The mixture was diluted with aqueous saturated ammonium chloride, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 5-40% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the solid, which was recrystallized from ethyl acetate/diisopropyl ether to give the title compound as a colorless crystal (363 mg, 0.855 mmol, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-922b1599650b435eb71d2fd87ce637c7
Source noteuspto-grants-2014_12