Reaktion #7506
ord-ebdb6c09cb774332a0a1cecc00fe64cd
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeobtained
- 2Temperaturcooled
- 3Filtrationfiltered over dicalite
- 4SonstigeThe filtrate was separated into its layers
- 5WaschenThe organic layer was washed with H2O
- 6Trocknendried (MgSO4)
- 7Filtrationfiltered
- 8Sonstigethe solvent was evaporated
- 9SonstigeThe residue was purified over silica gel on a glass
- 10Filtrationfilter (eluent: CH2Cl2/CH3OH 100/0 to 97/3)
- 11SonstigeThe pure fractions were collected
- 12Sonstigethe solvent was evaporated
Vorschrift
A mixture of 5,10-dihydro-imidazo[1,2-b]-isoquinoline-7,8-diol, obtained according to the procedure described in Ex.No. A8 c, (0.155 mol), phenyltrimethylammonium chloride (0.31 mol) and K2CO3 (0.68 mol) in DMF (400 ml) was stirred at 90° C. for 20 hours, cooled, poured out into H2O and filtered over dicalite. The filtrate was separated into its layers. The organic layer was washed with H2O, dried (MgSO4), filtered and the solvent was evaporated. The residue was purified over silica gel on a glass filter (eluent: CH2Cl2/CH3OH 100/0 to 97/3). The pure fractions were collected and the solvent was evaporated, yielding 3 g of 5,10-dihydro-7,8-dimethoxyimidazo[1,2-b]isoquinoline (8.4%) (interm. 22).