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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348635Generated: October 30, 2026

Sodium Hydroxide → (4-{[bis(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-(4-dipropylaminomethylphenyl)-amine

https://huagongshe.com/reaction/348635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Methyl-2-imidazolecarboxaldehydeHCID 139575—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(4-Aminomethylbenzyl)-(4-dipropylaminomethylphenyl)-amineHCID 23079293—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product(4-{[bis(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-(4-dipropylaminomethylphenyl)-amineHCID 58801914122.1%

Reaction Steps

The compound (57.3 mg) obtained in Example 39-2 was dissolved in methanol (2.5 ml). The solution was added with 1-methyl-2-imidazole carboxaldehyde (158 mg) and then added with sodium cyanoborohydride (68.4 mg). The reaction solution was adjusted to pH 5 by the addition of acetic acid, followed by stirring for 17 hours at room temperature. Then, the reaction solution was added with a 1 mol/l sodium hydroxide aqueous solution and then subjected to extraction with chloroform. After that, the organic layer was washed with saturated saline solution and then dried with anhydrous sodium sulfate. After the solvent had been distilled off, a 10% hydrogen chloride/methanol solution was added to the residue, and the solvent was then distilled off. The residue obtained was purified through silica gel column chromatography (chloroform/methanol/water), thereby obtaining the subject compound (55.2 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176227B2
Source datasetuspto-grants-2007_02
ORD IDord-0d1f158ecc154a12bc1e9337dbb4b01e
Source noteuspto-grants-2007_02