Trifluoroacetic acid → HCID 15228076、化合物
反応式
[CH3:1][CH2:2][O:3][CH2:4][CH2:5][N:6]1[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[C:15]([CH:17]1[CH2:22][CH2:21][N:20](C(OC(C)(C)C)=O)[CH2:19][CH2:18]1)=[O:16].FC(F)(F)C(O)=O.C(=O)([O-])O.[Na+]>>[CH3:1][CH2:2][O:3][CH2:4][CH2:5][N:6]1[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[C:15]([CH:17]1[CH2:18][CH2:19][NH:20][CH2:21][CH2:22]1)=[O:16]参加物
4
実験手順
Mix 1-[[(2-ethoxy)ethyl]-1H-benzimidazol-2-yl][1-(t-butyloxycarbonyl)-4-piperidinyl]methanone (10.07 g, 26.67 mmol) and trifluoroacetic acid (75 mL). Stir at room temperature until the reaction is complete. Pour onto water and carefully neutralize with solid sodium hydrogen carbonate. Extract into ethyl acetate (2×), wash with brine and dry (MgSO4). Evaporate the solvent in vacuo and purify by chromatography to give the title compound.
後処理
- additionPour onto water
- extractionExtract into ethyl acetate (2×)
- washwash with brine
- dry with materialdry (MgSO4)
- customEvaporate the solvent in vacuo
- custompurify by chromatography
出典と根拠
- ORDレコード
- ord-c2a19692b3094a1c9b0b889db26201ea
- 出典データセット
- uspto-grants-1995_01
- 特許番号
- US05380731
反応ノート
読み込み中…