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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382355Generated: October 31, 2026

Methyl iodide → 2-(4-Methoxyphenyl)-1-methyl-1H-benzimidazole-4-carboxamide

https://huagongshe.com/reaction/382355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178488846HCID 178488846—
SolventAcetoneHCID 180—
Product2-(4-Methoxyphenyl)-1-methyl-1H-benzimidazole-4-carboxamideHCID 10540772—

Reaction Steps

2-(4′-Methoxyphenyl)benzimidazole-4-carboxamide (NU1076 from Example 5) (105.3 mg, 0.394 mmol) and powdered potassium hydroxide (22 mg, 0.394 mmol) were suspended in acetone (4 ml) and stirred until all the solids had dissolved. Methyl iodide (24.6 μll, 0.394 mmol) was added and the reaction stirred at room temperature overnight. The solvent was removed under reduced pressure and the white solid residue purified by column chromatography with dichloromethane/methanol 95:5 to give fine white crystals of the title compound. (33.2 mg, 30%) mp 289-292° C.; Found C 68.62 H 5.36 N 14.67 C16Hl5N3O2 Requires C 68.33 H 5.34 N 14.95; vmax(cm−1) 3309.23, 3141.44, 1671.29, 1605.30, 1255.08, δH 3.95 (3H, s), 4.02 (3H, s), 7.22-7.27 (2H, d), 7.44-7.52 (1H, t), 7.86-8.00 (5H, m), 9.4 (1H, br s, NH); m/z (EI) 281 (M+), 264, 250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310082B1
Source datasetuspto-grants-2001_10
ORD IDord-056a59c1f9a940fd87e11548b35443a8
Source noteuspto-grants-2001_10