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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404477Generated: October 31, 2026

Methyl iodide → HCID 66836080, compound

https://huagongshe.com/reaction/2404477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 56947596HCID 56947596—
SolventAcetoneHCID 180—
SolventAcetonitrileHCID 6342—
ProductHCID 66836080HCID 66836080—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-[(3-iodophenyl)(1-methylpiperidin-4-yloxy)methyl]-1H-benzimidazole (example 51, 260 mg) in anhydrous acetonitrile (10 mL) is treated with 60% sodium hydride (47 mg) for 1 h at room temperature. The mixture is then cooled to 0° C. and iodomethane (36 μL) is introduced. After stirring for 15 h, dilution with water and extraction with ethyl acetate, the organic phase is dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography over silica gel (gradient dichloromethane/methanol/ammonia from 95/5/0.5 to 90/10/0.5) to afford the pure base that is then converted into its dioxalate salt in acetone to give 2-[(3-iodophenyl)(1-methylpiperidin-4-yloxy)methyl]-1-methyl-1H-benzimidazole, dioxalate, melting at 76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802664B2
Source datasetuspto-grants-2014_08
ORD IDord-9536d8b8b57c4908a0ef6e38daf3035a
Source noteuspto-grants-2014_08