Potassium Carbonate → (R)-5-Dipropylamino-1-methoxy-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one
Reaction equation
[CH2:1]([NH:4][C@@H:5]1[CH2:14][C:13]2[C:8]3=[C:9]([N:15]([O:18][CH3:19])[C:16](=[O:17])[N:7]3[CH2:6]1)[CH:10]=[CH:11][CH:12]=2)[CH2:2][CH3:3].I[CH2:21][CH2:22][CH3:23].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH2:1]([N:4]([CH2:21][CH2:22][CH3:23])[C@@H:5]1[CH2:14][C:13]2[C:8]3=[C:9]([N:15]([O:18][CH3:19])[C:16](=[O:17])[N:7]3[CH2:6]1)[CH:10]=[CH:11][CH:12]=2)[CH2:2][CH3:3]Participants
Procedure
Following the procedure of Example 3, a mixture of (R)-5-Propylamino-1-methoxy-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (8b, 0.93 g, 3.56 mmol) 1-iodopropane (3.05 g, 17.9 mmol), and potassium carbonate (1.97 g, 14.3 mmol) in acetonitrile (25 ml) was heated at reflux under nitrogen for 17 hours. 1-Iodopropane (3.05 g, 17.9 mmol) was again added, and the mixture was refluxed for an additional 5 hours. The solvent was removed under vacuum, and the mixture was diluted with water and extracted twice with diethylether. The organic extract was washed with brine and dried (MgSO4). The solvent was removed under vacuum to leave an amber oil. Purification by flash chromatography (230-400 mesh silica gel; 10-25% ethyl acetate in hexane) gave the title compound (9b) as an amber oil (0.87 g, 90% yield).
Workup
- temperaturewas heated
- temperatureat reflux under nitrogen for 17 hours
- temperaturethe mixture was refluxed for an additional 5 hours
- customThe solvent was removed under vacuum
- additionthe mixture was diluted with water
- extractionextracted twice with diethylether
- extractionThe organic extract
- washwas washed with brine
- dry with materialdried (MgSO4)
- customThe solvent was removed under vacuum
- customto leave an amber oil
- customPurification by flash chromatography (230-400 mesh silica gel; 10-25% ethyl acetate in hexane)
Sources & evidence
- ORD record
- ord-7da89412939b4260a7af21c081d87f73
- Source dataset
- uspto-grants-2004_03
- Patent number
- USRE038452E1
Reaction notes
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