Phosphorus oxychloride → 2-(5-(4-Chloro-2-((3-fluorophenyl)amino)pyrimidin-5-yl)-4-pentyn-1-yl)isoindoline-1,3-dione

HRID 2284757ノート

反応式

HRID 2284757 の反応式
[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]=1

参加物

4

反応条件

温度
80 °C

実験手順

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.

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. additionpoured into ice
  3. customThe organic layer was separated
  4. washwashed successively with water, saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride
  5. dry with materialdried over anhydrous sodium sulfate
  6. customthe solvent was evaporated under reduced pressure
  7. washThe obtained solid matter was washed with diisopropyl ether
  8. customdried under reduced pressure

出典と根拠

ORDレコード
ord-56a210e8aa0d494da22985f5176933d4
出典データセット
uspto-grants-2015_09
特許番号
US09145415B2

反応ノート

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