HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277704Generated: October 30, 2026
HCID 11481734, compound → HCID 9871847, compound
https://huagongshe.com/reaction/277704
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11481734 | HCID 11481734 | — |
| Reactant | HCID 53702815 | HCID 53702815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9871847 | HCID 9871847 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06358949B1 |
|---|
| Source dataset | uspto-grants-2002_03 |
|---|
| ORD ID | ord-c718ea203ec34a82ba99642a4376fc2e |
|---|
| Source note | uspto-grants-2002_03 |
|---|