[CH2:1]([C@H:8]([NH2:25])[CH2:9][N:10]1[CH2:15][CH2:14][CH:13]([O:16][C:17]2[CH:22]=[CH:21][C:20]([F:23])=[C:19]([F:24])[CH:18]=2)[CH2:12][CH2:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[N:32]1[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=1[C:38]1[S:42][C:41]([S:43](Cl)(=[O:45])=[O:44])=[CH:40][CH:39]=1.O>CC(C)=O>[CH2:1]([C@H:8]([NH:25][S:43]([C:41]1[S:42][C:38]([C:33]2[CH:34]=[CH:35][CH:36]=[CH:37][N:32]=2)=[CH:39][CH:40]=1)(=[O:44])=[O:45])[CH2:9][N:10]1[CH2:11][CH2:12][CH:13]([O:16][C:17]2[CH:22]=[CH:21][C:20]([F:23])=[C:19]([F:24])[CH:18]=2)[CH2:14][CH2:15]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1The product of Example 6, Step (a) (0.091 g) was dissolved in acetone (2 ml). Potassium carbonate [0.066 g dissolved in H2O (0.5 ml)] was then added, followed by 5-pyridin-2-yl-thiophene-2-sulfonyl chloride (0.067 g) and the reaction left to stir for 10 mins. Water was then added and the product extracted with ethyl acetate. The combined organic extracts dried, filtered and concentrated. Purification by flash silica column chromatography with 1% MeOH/98.9% CH2Cl2/0.1% aq NH3 as eluent, and then reverse phase HPLC {with a gradient eluent system [50% MeCN/NH4OAcaq (0.1%) to 70% MeCN//NH4OAcaq (0.1%)]} gave the title compound as a solid (0.057 g).
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