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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 703383Erstellt: 24. Oktober 2026

Glutaric Acid → HCID 178512976, Verbindung

https://huagongshe.com/de/reaction/703383

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGlutaric AcidHCID 743—
EduktGlyoxylylspermidineHCID 133564—
EduktHCID 178479464HCID 178479464—
EduktN-[4-(3-aminopropyl)aminobutyl]-2-(4-guanidinobutanamido)-2-hydroxyethanamide hydrochlorideHCID 178479465—
LösungsmittelWaterHCID 962—
ProduktHCID 178512976HCID 17851297635%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 360 mg (2 mmoles) of 4-guanidinobutanamide hydrochloride, 701 mg (2.4 mmoles) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride, 264 mg (2 mmoles) of glutaric acid and 0.36 ml of water was heated at 60° C. for 24 hours. After completion of the reaction, 5 ml of water was added to the reaction mixture, then passed through a column (20 mm inner diameter) packed with 150 ml of CM-Sephadex® C-25 (Na-type), and fractionated by the gradient elution method with 1.5 liters of water and 1.5 liters of 0.8M aqueous sodium chloride solution (15 ml fraction size). The fractions No. 125 to No. 137 corresponding to the sodium chloride concentrations of 0.48-0.56M were combined, then concentrated, and extracted three times with 10 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). The fractions No. 9 to No. 15 were combined and evaporated to dryness, yielding 318 mg (35% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(4-guanidinobutanamido)-2-hydroxyethanamide hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04983328
Quelldatensatzuspto-grants-1991_01
ORD IDord-2fbbc436b07d429ab950345fc8b80bc1
Quellennotizuspto-grants-1991_01