Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649893Generated: October 30, 2026

2,4-Dimethoxybenzoyl chloride → HCID 9826690, compound

https://huagongshe.com/reaction/649893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethoxybenzoyl chlorideHCID 2734719—
ReactantHCID 15546371HCID 15546371—
SolventDichloromethaneHCID 6344—
ProductHCID 9826690HCID 982669095%

Reaction Steps

A solution of 5.4 mmole 2-(chloromethyl)-1-[(2-methylphenyl)methyl]benzimidazole in 20 mL of dry Acetonitrile is treated with 10 mL of isoamylamine for 16 hr at room temperature. The solvent is removed in vacuo and the residue is partitioned between 30 mL of ethyl acetate and 10 mL of 1 N NaOH. The ethyl acetate layer is dried over anhydrous Na2SO4 and solvent removed in vacuo to afford 1.6 g 92% ({1-[(2-methylphenyl)methyl]benzimidazol-2-yl}methyl) (3-methylbutyl)amine. 2,4-dimethoxybenzoylchloride 1.5 eq is treated with 1.0 eq of ({1-[(2-methylphenyl)methyl]benzimidazol-2-yl}methyl) (3-methylbutyl)amine in dichloromethane at room temperature for 1 hr. The reaction is quenched with 1 N NaOH and partitioned between dichloromethane and water. The organic layer is dried with Na2SO4 and the solvent removed in vacuo. The residue is chromatographed (SiO2) with ethyl acetate to afford 95% of (2,4-dimethoxyphenyl)-N-({1-[(2-methylphenyl)methyl]benzimidazol-2-yl}methyl)-N-(3-methylbutyl)carboxamide (Compound 1). Mass Spec M+ 486.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271241B1
Source datasetuspto-grants-2001_08
ORD IDord-0a7166f967024db18b39637927520e06
Source noteuspto-grants-2001_08