HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 255807Erstellt: 24. Oktober 2026
Glycolic Acid → 1H-Pyrano(3',4':6,7)indolizino(1,2-b)quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-11-(hydroxymethyl)-, (S)-
https://huagongshe.com/de/reaction/255807
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Glycolic Acid | HCID 757 | — |
| Edukt | Camptothecin | HCID 24360 | — |
| Edukt | Ammonium Persulfate | HCID 62648 | — |
| Katalysator | Silver Nitrate | HCID 24470 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | 1H-Pyrano(3',4':6,7)indolizino(1,2-b)quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-11-(hydroxymethyl)-, (S)- | HCID 149610 | — |
Reaktionsschritte
Camptothecin (50 mg, 0.143 m-mol) was dissolved in 75% sulfuric acid (3 ml). To this solution were added glycolic acid (500 mg, 6.57 m-mol) and silver nitrate (250 mg, 1.31 m-mol) and then was added dropwise under heating (100°-110° C.) and agitation and aqueous solution (15 ml) of ammonium persulfate (3.00 g, 0.0131 m-mol) over 2 hours. After the reaction mixture was allowed to cool, ice water (100 ml) was poured into the reaction mixture which was then extracted with chloroform (100 ml×3). The chloroform layers were combined, washed with a 7% aqueous solution of sodium bicarbonate (300 ml) and then with a saturated edible salt solution (100 ml), dried with anhydrous magnesium sulfate, filtered and evaporated until dryness under reduced pressure. The residue was subjected to thin layer chromatography (5% methanol-chloroform) to effect separation and purification of 7-hydroxymethylcamptothecin whereupon 10.3 mg (19.0%) of pure 7-hydroxymethylcamptothecin were obtained. Besides this, 10.7 mg of camptothecin were recovered.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | USRE032518 |
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| Quelldatensatz | uspto-grants-1987_10 |
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| ORD ID | ord-fc5023fe01dc4785a66e34e5a83e4190 |
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| Quellennotiz | uspto-grants-1987_10 |
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