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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173891Generated: November 1, 2026

1H-imidazole-2-carbaldehyde → (4-dipropylaminomethylphenyl)-(4-{[(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-amine

https://huagongshe.com/reaction/1173891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
Reactant(4-Aminomethylbenzyl)-(4-dipropylaminomethylphenyl)-amineHCID 23079293—
SolventMethanolHCID 887—
Product(4-dipropylaminomethylphenyl)-(4-{[(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)-amineHCID 2108447359.8%

Reaction Steps

The compound (63.1 mg) obtained in Example 39-2 was dissolved in methanol (2.0 ml) and then added with 2-imidazole carboxaldehyde (17.9 mg), followed by stirring at room temperature for 17 hours. After the solvent had been distilled off, the residue was dried under vacuum and then dissolved in methanol (2.5 ml). Subsequently, the solution was added with sodium borohydride (14.5 mg) and stirred at room temperature for 1 hour. The reaction solution was added with a saturated aqueous ammonium chloride solution (4.0 ml) and stirred at room temperature for 30 minutes. Then, the reaction solution was added with saturated saline solution and subjected to extraction with chloroform, followed by drying with anhydrous sodium sulfate. After the solvent had been distilled off, the residue obtained was purified through silica gel column chromatography (chloroform/acetone), thereby obtaining the subject compound (45.2 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-409b1dc7c0444ba18f4ee8bc0b230cec
Source noteuspto-grants-2010_11