反応式
[Br:1][C:2]1[CH:7]=[C:6]([C:8]([OH:10])=O)[CH:5]=[CH:4][C:3]=1[C:11]1[CH:16]=[C:15]([C:17]([F:20])([F:19])[F:18])[CH:14]=[C:13]([C:21]([F:24])([F:23])[F:22])[CH:12]=1.CCN=C=N[CH2:30][CH2:31][CH2:32][N:33]([CH3:35])C.Cl.O[N:38]1[C:42]2[CH:43]=[CH:44][CH:45]=CC=2N=N1.[CH3:47]N(C=O)C>>[Br:1][C:2]1[CH:7]=[C:6]([C:8]([N:38]2[CH2:45][CH2:44][CH:43]([C:47]3[CH:35]=[N:33][CH:32]=[CH:31][CH:30]=3)[CH2:42]2)=[O:10])[CH:5]=[CH:4][C:3]=1[C:11]1[CH:16]=[C:15]([C:17]([F:20])([F:19])[F:18])[CH:14]=[C:13]([C:21]([F:24])([F:23])[F:22])[CH:12]=1参加物
5
反応物 4
生成物 1
実験手順
i-5d (179 mg, 1.21 mmol) was added to a stirred solution of 3a (500 mg, 1.21 mmol), N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (255 mg, 1.33 mmol) and 1-hydroxybenzotriazole 185 mg, 1.21 mmol) in DMF (8.00 mL). After 4 h, the reaction mixture was quenched with said, aq. NaHCO3 and extracted with EtOAc. The organic layer was washed with water and brine, dried (sodium sulfate) and concentrated in vacuo. The resulting crude residue was purified by column chromatography on silica gel (gradient elution; 0%-5% methanol/EtOAc as eluent) to afford the title compound 3b. m/z (ES) 543 (MH)+.
後処理
- customthe reaction mixture was quenched
- extractionaq. NaHCO3 and extracted with EtOAc
- washThe organic layer was washed with water and brine
- dry with materialdried (sodium sulfate)
- concentrationconcentrated in vacuo
- customThe resulting crude residue was purified by column chromatography on silica gel (gradient elution; 0%-5% methanol/EtOAc as eluent)
出典と根拠
- ORDレコード
- ord-565eb4acbea748179c320f971fd30d70
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367679B2
関連ノート
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