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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173946Generated: November 2, 2026

Sodium Hydroxide → HCID 10438338, compound

https://huagongshe.com/reaction/1173946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-[4-(dipropylamino)phenyl]-4-[(1H-imidazol-2-ylmethylamino)methyl]benzamideHCID 21084514—
ReactantHCID 23079305HCID 23079305—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 10438338HCID 10438338139.1%

Reaction Steps

The compound (120 mg) obtained in Example 47-3 was dissolved in methanol (5.0 ml). The solution was added with the compound (73.0 mg) obtained in Example 92-2 and sodium cyanoborohydride (18.0 mg) and then adjusted to pH 5 with acetic acid, followed by stirring at room temperature for 2 days. After completion of the reaction, the reaction solution was added with a 1 mol/l sodium hydroxide aqueous 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), thereby obtaining the subject compound (121 mg) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-8355e55971384500a71c3ccb1b6ce663
Source noteuspto-grants-2010_11