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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 462905Erstellt: 24. Oktober 2026

Hydrochloric Acid → 8-Guanidino-3-hydroxyoctanamide hydrochloride

https://huagongshe.com/de/reaction/462905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBis(S-methylisothiouronium) sulfateHCID 13347—
Edukt8-Amino-3-hydroxyoctanamide hydrochlorideHCID 22149892—
LösungsmittelSodium HydroxideHCID 14798—
Produkt8-Guanidino-3-hydroxyoctanamide hydrochlorideHCID 178479437113,3%

Reaktionsschritte

To a solution of 670 mg of 8-amino-3-hydroxyoctanamide hydrochloride in 8 ml of 1N aqueous sodium hydroxide solution, was added 668 mg (2.4 mmoles) of S-methylisothiourea hemisulfate. The mixture was stirred overnight at room temperature. The reaction mixture was adjusted to pH 6 with 1N hydrochloric acid, evaporated to dryness and dissolved in 5 ml of 1M saline. The solution was passed through a column of 160 ml of Diaion® HP-20 (Mitsubishi Chemical Co.) and the column was eluted successively with 400 ml of 1M saline, 400 ml of 0.8M saline and 800 ml of 0.6M saline (15 g fraction size). Fractions No. 41 to No. 87 were combined, evaporated to dryness and extracted three times with 10 ml of methanol. The methanol layer was passed through a column of 300 ml of Sephadex® LH-20 and eluted with methanol to effect desalting (7 ml fraction size). Fractions No. 25 to 35 were combined and evaporated to dryness to obtain 687 mg (85% yield) of 8-guanidino-3-hydroxyoctanamide hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04518532
Quelldatensatzuspto-grants-1985_05
ORD IDord-17387d8a505046deb755ca3a22d61c2b
Quellennotizuspto-grants-1985_05