[C:1]([O:5][C:6]([N:8]1[CH2:11][C:10]([OH:13])([CH3:12])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].[Br:16][C:17]1[CH:28]=[CH:27][C:20]([CH:21]=NC(C)(C)C)=[C:19](F)[CH:18]=1.CS(C)=[O:32]>O>[C:1]([O:5][C:6]([N:8]1[CH2:11][C:10]([O:13][C:27]2[CH:28]=[C:17]([Br:16])[CH:18]=[CH:19][C:20]=2[CH:21]=[O:32])([CH3:12])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]To a solution of the title compound from Step B (400 mg, 2.2 mmol) in DMSO (8 mL) was added 60% NaH (120 mg, 3.0 mmol). After 30 min, the title compound from Step A was added and the resulting mixture was heated at 125° C. for 1 h in a microwave reactor. An additional quantity of the title compound from Step B (100 mg) and 60% NaH (32 mg) were added to the reaction. Heating was then resumed at 125° C. for another 1 h in a microwave reactor. The reaction was diluted with H2O and extracted with EtOAc (3×) followed by methanolic EtOAc (2×). The organics were dried, then THF (5 mL), H2O (5 mL) and AcOH (3 mL) were added. After 18 h at rt, the reaction was diluted with H2O and extracted with CH2Cl2. The organics were dried and purified by PTLC to give the title compound as an off white solid (247 mg, 31%). 1H NMR (CDCl3): 10.36 (s, 1H), 7.74 (d, J=8.3 Hz, 1H), 7.22-7.20 (m, 1H), 6.68 (d, J=1.6 Hz, 1H), 4.25 (d, J=9.2 Hz, 2H), 4.03 (d, J=9.8 Hz, 2H), 1.55 (s, 3H), 1.46 (m, 9H).
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