Hydrochloric Acid → Ethyl 10-(ethylamino)-4-oxo-3-((phenylcarbonyl)oxy)-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxylate

HRID 1093085Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1093085
[CH2:1]([N:8](CC)[C:9]12[CH2:17][CH2:16][CH:13]([CH2:14][CH2:15]1)[CH2:12][N:11]1[C:18](=[O:36])[C:19]([O:27][C:28]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[O:29])=[C:20]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[N:21]=[C:10]21)[C:2]1C=CC=CC=1.Cl.[H][H]>CO.[Pd]>[CH2:1]([NH:8][C:9]12[CH2:17][CH2:16][CH:13]([CH2:14][CH2:15]1)[CH2:12][N:11]1[C:18](=[O:36])[C:19]([O:27][C:28]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[O:29])=[C:20]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[N:21]=[C:10]21)[CH3:2]

Komponenten

6

Versuchsvorschrift

To a mixture of ethyl 10-(benzyl(ethyl)amino)-4-oxo-3-((phenylcarbonyl)oxy)-4,6,7,8,9,10-hexahydro-7,10-ethanopyrimido[1,2-a]azepine-2-carboxylate (120 mg, 0.233 mmol) in methanol (5 mL) was added 1N HCl (0.256 mL, 0.256 mmol) followed by Pd/C (24.77 mg, 0.023 mmol) and the mixture stirred under 1 atm hydrogen for 18 h. The mixture was filtered and the solids thoroughly washed with dichloromethane. The filtrate was concentrated under reduced pressure and dried under high vacuum overnight to afford the title compound.

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. washthe solids thoroughly washed with dichloromethane
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customdried under high vacuum overnight

Quellen und Nachweise

ORD-Eintrag
ord-f11a9c1fdb3d4a3e95dd4450e8cbde49
Quelldatensatz
uspto-grants-2012_03
Patentnummer
US08129398B2

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