Water → HCID 87130437, compound
Reaction equation
[Li][CH2:2]CCC.[F:6][C:7]1C=NC2[C:15]([CH:16]=1)=CC(OC)=CC=2.C[N:20]([CH:22]=O)[CH3:21].O.[CH2:25]1[CH2:29][O:28][CH2:27][CH2:26]1>>[F:6][C:7]1[CH:16]=[CH:15][C:21]2[N:20]=[CH:22][CH:2]=[CH:27][C:26]=2[C:25]=1[CH:29]=[O:28]Participants
Conditions
- Temperature
- -78 °C
Procedure
To a solution of DIPA (1.1 mL, 7.75 mmol)) in THF (820 mL) cooled to −78° C., was added n-BuLi (2.5N in hexanes, 3 mL). The mixture was stirred 5 minutes at this temperature and was warmed in an ice-bath. After 10 min, the mixture was cooled down to −78° C. and a solution of 3-fluoro-6-methoxy-quinoline (see WO 2005/054232; 0.95 g, 6.46 mmol) in THF (8+2 mL rinse) was added. The reaction proceeded for 4 h. DMF (0.75 mL, 9.68 mmol) was added. The mixture was stirred 30 min at −78° C. The mixture was warmed to rt, stirred further 30 min and water (20 mL) was added. The two layers were decanted. The aq. layer was extracted with EA (2×50 mL). The combined org. layers were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was chromatographed (Hept-EA 1-1) to afford first the starting material and then the expected aldehyde (0.17 g) as a 2-1 mixture with its regioisomer.
Workup
- temperaturewas warmed in an ice-bath
- waitAfter 10 min
- waitThe reaction proceeded for 4 h
- stirringThe mixture was stirred 30 min at −78° C
- temperatureThe mixture was warmed to rt
- stirringstirred further 30 min
- customThe two layers were decanted
- extractionThe aq. layer was extracted with EA (2×50 mL)
- washlayers were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated to dryness
- customThe residue was chromatographed (Hept-EA 1-1)
- customto afford first the starting material
Sources & evidence
- ORD record
- ord-7e0e37b9afc34c97941532b3194d0a35
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08114867B2
Reaction notes
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