1-Hydroxybenzotriazole → Artelinate

HRID 553405

Reaktionsgleichung

Reaktionsgleichung von HRID 553405
C[C@H]1[C@@H]2CCC3(C)OO[C@]42[C@H]([C@@H](C)[C@@H](O)O[C@@H]4O3)CC1.[CH3:21][C@@H:22]1[C@H:31]2[CH2:32][CH2:33][C@@:34]3([CH3:38])[O:36][O:37][C@@:30]42[C@H:25]([C@H:26]([CH3:50])[C@H:27]([O:39][CH2:40][C:41]2[CH:42]=[CH:43][C:44]([C:47]([OH:49])=[O:48])=[CH:45][CH:46]=2)[O:28][C@@H:29]4[O:35]3)[CH2:24][CH2:23]1.ON1C2C=CC=CC=2N=N1.C(N=C=NC(C)(C)C)C>C(#N)C>[CH3:21][C@H:22]1[C@@H:31]2[CH2:32][CH2:33][C:34]3([CH3:38])[O:36][O:37][C@:30]42[C@H:25]([C@@H:26]([CH3:50])[C@@H:27]([O:39][CH2:40][C:41]2[CH:46]=[CH:45][C:44]([C:47]([OH:49])=[O:48])=[CH:43][CH:42]=2)[O:28][C@@H:29]4[O:35]3)[CH2:24][CH2:23]1

Komponenten

6

Versuchsvorschrift

Attempts to prepare an hydrazide derivative of artesunate were unsuccessful and resulted in the formation of dihydroartemisinin due to the cyclization reaction. Artelinate was synthesized from dihydroartemisinin as previously described (Shrimali et al. (1998) Indian J. Chem. 37B:1161-1163). Artelinic acid (0.1 g, 0.24 mmol) was dissolved in anhydrous acetonitrile (0.48 mL). To this solution, 1-hydroxybenztriazole (HOBt) (0.038 g, 0.29 mmol) was added, followed by addition of ethyl dimethylethylcarbodiimide (0.055 g, 0.29 mmol). The reaction mixture was stirred at room temperature and monitored by thin-layer chromatography (TLC) until all the acid was converted to the HOBt ester.

Quellen und Nachweise

ORD-Eintrag
ord-c3defc15bea949658fc4a5ffc314abb0
Quelldatensatz
uspto-grants-2011_11
Patentnummer
US08048850B2

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