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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034286Generated: October 31, 2026

Methyl iodide → HCID 85612602, compound

https://huagongshe.com/reaction/1034286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 85612633HCID 85612633—
SolventTetrahydrofuranHCID 8028—
ProductHCID 85612602HCID 8561260211%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of N-cyclohexyl-N-methyl 4-(1H-benzimidazylmethyl)benzamide (347 mg, 1 mmol) in dry THF (20 ml) at -78 ° C. was added sodium bis(trimethylsilyl)amide (1.1 ml of 1M solution in THF) under argon. The mixture was left to stir at -78° C. for 40 minutes, a solution of methyl iodide (170 mg, 1.2 mmol) in dry THF (2 ml) was added and the mixture left to warm to ambient temperature overnight. The reaction mixture was partitioned between ethyl acetate and brine, the organic layer dried (Na2SO4), concentrated to give a crude product which was purified by column chromatography (flash silica gel, 4% methanol in DCM) to yield N-cyclohexyl-N-methyl 4-(1-(1H-benzimidazyl)ethyl)benzamide (40 mg, 11%) as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05314880
Source datasetuspto-grants-1994_05
ORD IDord-cf4e7b6967484aa4a995d8af425d4338
Source noteuspto-grants-1994_05