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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348690Generated: October 27, 2026

Sodium Hydroxide → N-[4-[(dipropylamino)methyl]phenyl]-4-[[(1-ethylimidazol-2-yl)methyl-(1H-imidazol-2-ylmethyl)amino]methyl]benzamide

https://huagongshe.com/reaction/348690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-ethyl-1H-imidazole-2-carbaldehydeHCID 11062377—
ReactantN-[4-(dipropylamino)phenyl]-4-[(1H-imidazol-2-ylmethylamino)methyl]benzamideHCID 21084514—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-[4-[(dipropylamino)methyl]phenyl]-4-[[(1-ethylimidazol-2-yl)methyl-(1H-imidazol-2-ylmethyl)amino]methyl]benzamideHCID 49771572—

Reaction Steps

The compound (120 mg) obtained in Example 47-3 was dissolved in methanol (5.0 ml) and then added with the compound (58.0 mg) obtained in Example 90-1 and sodium cyanoborohydride (18.0 mg). Then, the solution was adjusted to pH 5 with acetic acid and then stirred at room temperature for 2 days. After completion of the reaction, a 1 mol/l sodium hydroxide aqueous solution was added to the reaction solution, followed by separation/extraction with chloroform. The organic layer was dried with anhydrous sodium sulfate and the solvent was then distilled off. The residue was purified through silica gel column chromatography (chloroform/methanol) and then treated with hydrochloric acid, thereby obtaining hydrochloride (107 mg) of the subject compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176227B2
Source datasetuspto-grants-2007_02
ORD IDord-cfad80e99b074f4abf711c1707994045
Source noteuspto-grants-2007_02