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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173871Generated: October 25, 2026

Propanal → HCID 10432329, compound

https://huagongshe.com/reaction/1173871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanalHCID 527—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(4-{[bis-(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-piperazin-1-yl-methanoneHCID 21084462—
SolventMethanolHCID 887—
ProductHCID 10432329HCID 10432329—

Reaction Steps

The compound (48.8 mg) obtained in Example 32-2 was dissolved in anhydrous methanol (1.0 ml) and then added with sodium cyanoborohydride (16.2 mg), trimethyl orthoformate (21.1 μl), propionaldehyde (13.9 μl), followed by stirring overnight at room temperature under a nitrogen atmosphere. After completion of the reaction, the solvent was distilled off and the residue was then dissolved in chloroform. A saturated aqueous sodium bicarbonate solution was added to the solution, followed by stirring. The resultant solution was subjected to extraction with chloroform and washed with a saturated aqueous sodium bicarbonate solution and saturated saline solution, and then the organic layer was dried with anhydrous sodium sulfate. The solvent was distilled off and the residue was then treated with hydrochloric acid. Subsequently, the treated product was purified through silica gel column chromatography (chloroform/methanol/water), thereby obtaining hydrochloride (33.2 mg) of the subject compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-824ce398f8f546a39bfc06a4c7512942
Source noteuspto-grants-2010_11