Sodium Hydroxide → (2-(1-Naphthylamino)-7-fluoro-6-benzoxazolyl)acetic acid
反応式
[C:1]1([NH:11][C:12]2[O:13][C:14]3[C:20]([F:21])=[C:19]([CH2:22][C:23]([O:25]C)=[O:24])[CH:18]=[CH:17][C:15]=3[N:16]=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>C1COCC1.CO>[C:1]1([NH:11][C:12]2[O:13][C:14]3[C:20]([F:21])=[C:19]([CH2:22][C:23]([OH:25])=[O:24])[CH:18]=[CH:17][C:15]=3[N:16]=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1参加物
4
実験手順
Methyl (2-(1-naphthylamino)-7-fluoro-6-benzoxazolyl)acetate (1.41 g, 4.02 mmol) was dissolved in THF/methanol (21, 30 ml). To the resulting solution was added 1N NaOH (10 ml). After stirring at room temperature for 12 hours, the reaction mixture was distilled under reduced pressure to remove the solvent. The residue was acidified with 1N HCl. The crystals thus precipitated were collected by filtration under reduced pressure, washed with water and dried under reduced pressure to give (2-(1-naphthylamino)-7-fluoro-6-benzoxazolyl)acetic acid (1.44 g, 100%) as a brown solid.