Formic Acid → Amitiza

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[CH3:1][CH2:2][CH2:3][CH2:4][C:5]([F:27])([F:26])[C@:6]1([OH:25])[O:11][C@@H:10]2[CH2:12][C:13]([C@H:15]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]([OH:24])=[O:23])[C@H:9]2[CH2:8][CH2:7]1)=[O:14].C(N)(C)(C)C.C(O)=O>C(OCC)(=O)C.O>[CH3:1][CH2:2][CH2:3][CH2:4][C:5]([F:27])([F:26])[C@:6]1([OH:25])[O:11][C@@H:10]2[CH2:12][C:13]([C@H:15]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]([OH:24])=[O:23])[C@H:9]2[CH2:8][CH2:7]1)=[O:14]

참가 물질

실험 절차

To a solution of compound 10 (150 g) in dichloromethane (15 volumes), was added 10% palladium on carbon (35% wt) and the suspension was hydrogenated at 2 PSI for 15 hours. After the completion of the reaction, the mixture was filtered through Celite®, concentrated to near dryness and purified by column chromatography (ethyl acetate in hexanes) to give crude Lubiprostone. To a solution of crude Lubiprostone in ethyl acetate (10 vol) was added tert-butylamine (1.05 eq) at room temperature. The mixture was stirred at room temperature until precipitation of the amine salt occurred. The amine salt was isolated by filtration and dried to give Lubiprostone tert-butylamine salt (20 g). The amine salt was suspended in ethyl acetate (6 volumes) and water (3 volumes). The resulting bi-phasic mixture was adjusted to about pH 5 with formic acid. The organic layer was separated and concentrated to obtain Lubiprostone as a syrup. Upon crystallization using ethyl acetate/petroleum ether (1:9 volumes), the syrup produced Lubiprostone (1, 12 g) in approximately 70% recovery. The Lubiprostone filtrate was concentrated to near-dryness. HRMS (ESI+) [M+NH4]+ of (1): Formula: C20H36F2NO5: cal m/z: 408.25561 amu. found: 408.25626 amu.