[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]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.
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