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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348759Generated: October 29, 2026

Trimethyl orthoformate → [4-(6-{[(1H-imidazol-2-ylmethyl)amino]methyl}-1-propyl-1H-benzimidazol-2-yl)butyl]dipropylamine

https://huagongshe.com/reaction/348759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
ReactantSodium borohydrideHCID 4311764—
Reactant[4-(6-aminomethyl-1-propyl-1H-benzimidazol-2-yl)butyl]dipropylamineHCID 23079304—
SolventMethanolHCID 887—
Product[4-(6-{[(1H-imidazol-2-ylmethyl)amino]methyl}-1-propyl-1H-benzimidazol-2-yl)butyl]dipropylamineHCID 2315544339.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

The compound (130 mg) obtained in Example 125-6 was dissolved in methanol (3.0 ml) and added with trimethyl orthoformate (0.130 ml) and 2-imidazole carboxaldehyde (37.3 mg), followed by stirring for 1 hour. Then, the solution was cooled to 0° C. The solution was added with sodium borohydride (21.5 mg) and stirred at room temperature for 3 hours. After completion of the reaction, the solvent was distilled off under reduced pressure and the residue was then dissolved in chloroform. The solution was washed with a 1 mol/l sodium hydroxide aqueous solution and then subjected to extraction with chloroform. The organic layer was washed with saturated saline solution and then dried with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure. Then, the residue was purified through silica gel column chromatography (chloroform/methanol), thereby obtaining the subject compound (64.0 mg) as a pale-yellow viscous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176227B2
Source datasetuspto-grants-2007_02
ORD IDord-38837e77bc0749fd8ca71b4603d17646
Source noteuspto-grants-2007_02