[CH3:1][O:2][C:3]1[C:4]([C:34]([F:37])([F:36])[F:35])=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([C:13]([N:15]([C:24]([O:26][CH3:27])=[O:25])[CH2:16][C:17]([O:19]C(C)(C)C)=[O:18])=[O:14])=[C:8]([O:28][CH2:29][C:30]([F:33])([F:32])[F:31])[CH:7]=[CH:6]2>C(O)=O.O>[CH3:1][O:2][C:3]1[C:4]([C:34]([F:35])([F:37])[F:36])=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([C:13]([N:15]([C:24]([O:26][CH3:27])=[O:25])[CH2:16][C:17]([OH:19])=[O:18])=[O:14])=[C:8]([O:28][CH2:29][C:30]([F:31])([F:32])[F:33])[CH:7]=[CH:6]2A suspension of N-[[6-methoxy-2-(2,2,2-trifluoroethoxy)-5-(trifluoromethyl)-1-naphthalenyl]carbonyl]-N-(methoxycarbonyl)glycine, 1,1-dimethylethyl ester (5.86 g, 10.9 mmol) in formic acid (135 mL) was stirred at room temperature under a dry nitrogen atmosphere. After 10 minutes, dissolution occurred. After 1 hour, the reaction mixture was diluted with water (1.5 L) and extracted with ether (2×400 mL). The extracts were combined and the ether was removed. The residue was suspended in water (100 mL) and filtered. The solid was washed with water (2×20 mL) and air dried. The crude product was recrystallized from chloroform to provide the title compound as a white powder (4.15 g, 79%), m.p. 186°-187° C.
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