Réaction #3773
ord-fbd154b2d6e642c8b3af3f1af09e77e0
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Autrequickly seal the vessel
- 2ExtractionExtract the reaction mixture with ethyl acetate
- 3ExtractionExtract the organic layer with saturated aqueous potassium carbonate solution (5×10 mL)
- 4ExtractionExtract with chloroform (5×15 mL)
- 5SéchageCombine the organic layers, dry over MgSO4
- 6Filtrationfilter
- 7Autreevaporate in vacuo
- 8Autreto give a residue
Mode opératoire
Combine (S)-7-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)]-1,2,6,7,8,12b-hexahydro-6-oxopyrido[2,1-a][2]benzazepine (32 mg, 0.09 mmol) and sulfuric acid (1.0 mL, 95-98%) in a pressure vessel. Add 96% formic acid (200 μL) and quickly seal the vessel. After 18 hours, add water (10 mL). Extract the reaction mixture with ethyl acetate. Extract the organic layer with saturated aqueous potassium carbonate solution (5×10 mL). Combine the aqueous layers and carefully acidify with aqueous 12M hydrochloric acid solution. Extract with chloroform (5×15 mL). Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 2/1 ethyl acetate/hexane containing 0.5% acetic acid to give the title compound. Rf =0.14 (silica gel, 2/1 ethyl acetate/hexane containing 0.5% acetic acid).