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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080771Generated: November 1, 2026

1H-imidazole-2-carbaldehyde → HCID 58345795, compound

https://huagongshe.com/reaction/2080771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
Reactant(1-methyl-1H-imidazol-2-yl)methanamineHCID 533842—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 23155582HCID 23155582—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 58345795HCID 5834579554.6%

Reaction Steps

The compound (31.2 mg) obtained in Example 18-6 was dissolved in methanol (1.0 ml) and added with acetic acid (30 μl) and 1-methyl-2-aminomethylimidazole (15.4 mg), and the whole was stirred at room temperature for 2 hours. Sodium cyanoborohydride (22.7 mg) was added thereto and the whole was stirred at room temperature for 15 hours. Furthermore, 2-imidazole carboxaldehyde (18.0 mg) was added thereto and the whole was stirred at room temperature for 18 hours. After completion of the reaction, the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform, washed with a saturated aqueous sodium hydrogen carbonate solution and a saturated saline solution, and dried with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure. The residue was purified through silica gel column chromatography (chloroform/methanol) and treated with hydrochloric acid, thereby obtaining a hydrochloride (25.6 mg) of the subject compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932281B2
Source datasetuspto-grants-2011_04
ORD IDord-672648bf983a481fa0958a161b58a86d
Source noteuspto-grants-2011_04