Phosphorus oxychloride → 2-(5-(4-Chloro-2-((3-fluorophenyl)amino)pyrimidin-5-yl)-4-pentyn-1-yl)isoindoline-1,3-dione
반응식
[F:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[N:14]=[C:13](O)[C:12]([C:16]#[C:17][CH2:18][CH2:19][CH2:20][N:21]3[C:29](=[O:30])[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[C:22]3=[O:31])=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1.P(Cl)(Cl)([Cl:34])=O>C(OCC)(=O)C>[Cl:34][C:13]1[C:12]([C:16]#[C:17][CH2:18][CH2:19][CH2:20][N:21]2[C:29](=[O:30])[C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[C:22]2=[O:31])=[CH:11][N:10]=[C:9]([NH:8][C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=2)[N:14]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
To 2-(5-(2-((3-fluorophenyl)amino)-4-hydroxypyrimidin-5-yl)-4-pentyn-1-yl)isoindoline-1,3-dione (J4, 36 mg), phosphorus oxychloride (1 mL) was added at room temperature, and the mixture was stirred at 80° C. for 45 minutes. The reaction mixture was cooled to room temperature, and then poured into ice, and then ethyl acetate was added to the mixture. The organic layer was separated, washed successively with water, saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained solid matter was washed with diisopropyl ether, and then dried under reduced pressure to obtain 2-(5-(4-chloro-2-((3-fluorophenyl)amino)pyrimidin-5-yl)-4-pentyn-1-yl)isoindoline-1,3-dione (J5, 21 mg) as pale yellow solid.
후처리
- temperatureThe reaction mixture was cooled to room temperature
- additionpoured into ice
- customThe organic layer was separated
- washwashed successively with water, saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride
- dry with materialdried over anhydrous sodium sulfate
- customthe solvent was evaporated under reduced pressure
- washThe obtained solid matter was washed with diisopropyl ether
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-56a210e8aa0d494da22985f5176933d4
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09145415B2
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