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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080890Generated: November 2, 2026

Formaldehyde → 5-dipropylamino-(2S)-[(4-{[(1H-imidazol-2-ylmethyl)-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-methyl-amino]-pentanoic acid ethyl ester

https://huagongshe.com/reaction/2080890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-[[(1H-imidazol-2-ylmethyl)-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl]-benzaldehydeHCID 86614918—
Reactant(2S)-amino-5-dipropylamino-pentanoic acid ethyl esterHCID 86614919—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product5-dipropylamino-(2S)-[(4-{[(1H-imidazol-2-ylmethyl)-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-methyl-amino]-pentanoic acid ethyl esterHCID 11664001—

Reaction Steps

The compound (54.2 mg) obtained in Example 92-3 and the compound (76.8 mg) obtained in Example 84-5 were dissolved in ethanol (4.3 ml) and added with acetic acid (80 μl). The solution was added with sodium cyanoborohydride (49.6 mg) and the whole was stirred at room temperature for 1.5 hours. The solution was added with a 36% formaldehyde aqueous solution (0.10 ml) and the whole was stirred at room temperature for 1 hour. After completion of the reaction, the solvent was distilled off and the residue was dissolved in chloroform and washed with a 1 mol/l sodium hydroxide aqueous solution, followed by extraction with chloroform. The organic layer was washed with a saturated saline solution and dried with anhydrous sodium sulfate. After filtration, the solvent was distilled off and the residue was purified through silica gel column chromatography (chloroform), thereby obtaining the subject compound (94.9 mg) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932281B2
Source datasetuspto-grants-2011_04
ORD IDord-e194081f6cea4dc599d24f2c4ca628aa
Source noteuspto-grants-2011_04