[F:1][C:2]1[C:10]2[N:9]=[C:8]([CH:11]([C:13]3[N:14]([CH3:39])[C:15]4[CH:21]=[C:20]([C:22]([NH:24][CH2:25][CH2:26][O:27][C:28]5[CH:38]=[CH:37][CH:36]=[CH:35][C:29]=5[C:30]([O:32]CC)=[O:31])=[O:23])[CH:19]=[CH:18][C:16]=4[N:17]=3)[CH3:12])[NH:7][C:6]=2[C:5]([F:40])=[C:4]([F:41])[CH:3]=1.[OH-].[Na+].Cl>CO>[F:1][C:2]1[C:10]2[N:9]=[C:8]([CH:11]([C:13]3[N:14]([CH3:39])[C:15]4[CH:21]=[C:20]([C:22]([NH:24][CH2:25][CH2:26][O:27][C:28]5[CH:38]=[CH:37][CH:36]=[CH:35][C:29]=5[C:30]([OH:32])=[O:31])=[O:23])[CH:19]=[CH:18][C:16]=4[N:17]=3)[CH3:12])[NH:7][C:6]=2[C:5]([F:40])=[C:4]([F:41])[CH:3]=1A mixture comprising ethyl 2-(2-{2-[I-(4,6,7-trifluoro-1H-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidazol-5-carbonylamino}ethoxy}benzoate (118 mg, 0.21 mmol), methanol (4 ml) and 2N sodium hydroxide (2.1 ml) was stirred at room temperature for 4 hours, neutralized with 2N hydrochloric acid (2.1 ml) and partitioned between ethyl acetate and saturated ammonium chloride. The aqueous layer was separated and extracted with ethyl acetate (X3). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to a white solid. The residue was dissolved in warm ethanol (10 ml) and 4M hydrogen chloride/dioxane solution. The solution was diluted with ethyl ether to give a precipitate. The precipitate was isolated and dried to give 2-(2-{2-[1-(4,6,7-trifluoro-1H-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid as a white solid; MS (LCMS) C27H22F3N5O4 m/e calc 537.50; found 538.4 (MH+).
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