HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 462905Erstellt: 24. Oktober 2026
Hydrochloric Acid → 8-Guanidino-3-hydroxyoctanamide hydrochloride
https://huagongshe.com/de/reaction/462905
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Bis(S-methylisothiouronium) sulfate | HCID 13347 | — |
| Edukt | 8-Amino-3-hydroxyoctanamide hydrochloride | HCID 22149892 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | 8-Guanidino-3-hydroxyoctanamide hydrochloride | HCID 178479437 | 113,3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04518532 |
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| Quelldatensatz | uspto-grants-1985_05 |
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| ORD ID | ord-17387d8a505046deb755ca3a22d61c2b |
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| Quellennotiz | uspto-grants-1985_05 |
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