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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703387Generated: October 30, 2026

Hydrochloride methanol → HCID 178496807, compound

https://huagongshe.com/reaction/703387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantHCID 178478613HCID 178478613—
ReactantHCID 178496808HCID 178496808—
SolventMethanolHCID 887—
ProductHCID 178496807HCID 17849680767%

Reaction Steps

To a solution of 45.5 mg (0.10 mmole) of N-[4-(3-aminopropyl)aminobutyl]-2-(4-guanidinobutanamido)-2-hydroxyethanamide trihydrochloride in 1 ml of anhydrous methanol was added 0.1 ml of 2N hydrogen chloride-methanol. The mixture was stirred at room temperature for 17 hours. The reaction mixture was concentrated under reduced pressure and dissolved in 3 ml of water. The resulting solution was passed through a column (20 mm inner diameter) packed with 150 ml of CM-Sephadex® C-25 and fractionated by the gradient elution method with each one liter of water and 1M aqueous sodium chloride solution (17 ml fraction size). The fractions No. 67 to No. 71 corresponding to the salt concentrations of 0.63-0.67M were combined, evaporated to dryness and extracted three times with 5 ml of methanol. The methanol layer was passed through a column (20 mm inner diameter) packed with 150 ml of Sephadex® LH-20 and developed with methanol (7 ml fraction size). Fractions No. 10 to No. 14 were combined and evaporated to dryness, yielding 31.4 mg (67% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(4-guanidinobutanamido)-2-methoxyethanamide trihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983328
Source datasetuspto-grants-1991_01
ORD IDord-20ed408ead504e559fb922b2c467c145
Source noteuspto-grants-1991_01