Trifluoroacetic acid → 5-(4-Fluorophenyl)-2-({6-[(methylamino)methyl]pyridin-2-yl}amino)thiophene-3-carboxamide
反応式
C(O[C:6](=O)[N:7]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([NH:16][C:17]2[S:18][C:19]([C:25]3[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=3)=[CH:20][C:21]=2[C:22]([NH2:24])=[O:23])[N:11]=1)C)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[F:31][C:28]1[CH:29]=[CH:30][C:25]([C:19]2[S:18][C:17]([NH:16][C:12]3[CH:13]=[CH:14][CH:15]=[C:10]([CH2:9][NH:7][CH3:6])[N:11]=3)=[C:21]([C:22]([NH2:24])=[O:23])[CH:20]=2)=[CH:26][CH:27]=1参加物
実験手順
To a solution of tert-butyl[(6-{[3-(aminocarbonyl)-5-(4-fluorophenyl)-2-thienyl]amino}pyridin-2-yl)methyl]methylcarbamate (90 mg, 0.197 mmol) in dichloromethane (0.4 mL) was added trifluoroacetic acid (0.4 mL) and the reaction was maintained at room temperature for 1 hour. The volatiles were removed in vacuo and the crude product was purified by reverse phase HPLC (20-90% acetonitrile/water with 0.05% trifluoroacetic acid). The appropriate fractions were diluted with ethyl acetate (50 mL) and saturated aqueous sodium bicarbonate (40 mL). The layers were separated and the organic layer was washed with saturated aqueous sodium bicarbonate (40 mL) and water (2×40 mL), dried over sodium sulfate, filtered and concentrated to yield the title compound.
後処理
- customThe volatiles were removed in vacuo
- customthe crude product was purified by reverse phase HPLC (20-90% acetonitrile/water with 0.05% trifluoroacetic acid)
- additionThe appropriate fractions were diluted with ethyl acetate (50 mL) and saturated aqueous sodium bicarbonate (40 mL)
- customThe layers were separated
- washthe organic layer was washed with saturated aqueous sodium bicarbonate (40 mL) and water (2×40 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-03c2f1ac3eee4d9e95faa0a7079af875
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367706B2
反応ノート
読み込み中…