HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099855Generated: November 3, 2026
4-Methoxybenzylamine → 2-methyl-1H-benzimidazole-5-carboxylic acid
https://huagongshe.com/reaction/2099855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 2-methyl-1H-benzimidazole-5-carboxylic acid | HCID 1132609 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-methyl-1H-benzimidazole-5-carboxylic acid | HCID 1132609 | 127% |
| Product | HCID 57878451 | HCID 57878451 | — |
Reaction Steps
To a dimethylformamide (20 ml) solution of 2-methylbenzimidazol-5-carboxylic acid (1.00 g) were added hydroxybenzotriazole (844 mg), 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (1.21 g) and 4-methoxyphenylmethylamine (1.33 g) at room temperature, and the reaction solution was stirred at room temperature for 18 hours. The reaction solution was concentrated under reduced pressure and the obtained residue was diluted with chloroform (20 ml). The organic layer was washed with saturated sodium hydrogen carbonate aqueous solution, water and saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate. The residue obtained by solvent evaporation under reduced pressure was subjected to silica gel column chromatography and eluted with chloroform-methanol (30:1 (v/v)) to obtain (4-methoxyphenylmethyl)amide of 2-methyl-1H-benzimidazol-5-carboxylic acid (1.27 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07569688B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-071c4b37e4c94153a634d1906011744a |
|---|
| Source note | uspto-grants-2009_08 |
|---|