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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277704Generated: October 30, 2026

HCID 11481734, compound → HCID 9871847, compound

https://huagongshe.com/reaction/277704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11481734HCID 11481734—
ReactantHCID 53702815HCID 53702815—
SolventDichloromethaneHCID 6344—
ProductHCID 9871847HCID 987184795%

Reaction Steps

A solution of 5.4 mmole 1-{[2-(chloromethyl)-benzimidazolyl]methyl}-2-methoxybenzene in 20 mL of dryacetonitrile is treated with 10 mL of isoamylamine for 16 hours 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 1.7 g 97% ({1-[(2-methoxyphenyl)methyl]benzimidazol-2-yl}methyl)(3-methylbutyl) amine. 2-Chloro-3,4-dimethoxybenzoylchloride (1.5 equ.) is treated with 1.0 equivalent of ({1-[(2-methoxyphenyl)methyl]benzimidazol-2-yl}methyl)(3-methylbutyl) amine in dichloromethane at room temperature for 1 hour. 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-chloro-3,4-dimethoxyphenyl)-N-({1-[(2-methoxyphenyl)methyl]benzimidazol-2-yl}methyl)-N-(3-methylbutyl)carboxamide (Compound 1). Mass Spec M+ 537.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358949B1
Source datasetuspto-grants-2002_03
ORD IDord-c718ea203ec34a82ba99642a4376fc2e
Source noteuspto-grants-2002_03