Methanol → Methyl 4-chloro-3-(3-{[5-cyano-2-propyl-4-(trifluoromethyl)-1H-indol-1-yl]methyl}-1,2,4-oxadiazol-5-yl)benzoate

HRID 2102111ノート

反応式

HRID 2102111 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](I)=[CH:4][C:3]=1[C:9]1[O:13][N:12]=[C:11]([CH2:14][N:15]2[C:23]3[C:18](=[C:19]([C:26]([F:29])([F:28])[F:27])[C:20]([C:24]#[N:25])=[CH:21][CH:22]=3)[CH:17]=[C:16]2[CH2:30][CH2:31][CH3:32])[N:10]=1.[CH3:33][OH:34].CN([CH:38]=[O:39])C>CC([O-])=O.CC([O-])=O.[Pd+2]>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:33]([O:39][CH3:38])=[O:34])=[CH:4][C:3]=1[C:9]1[O:13][N:12]=[C:11]([CH2:14][N:15]2[C:23]3[C:18](=[C:19]([C:26]([F:28])([F:29])[F:27])[C:20]([C:24]#[N:25])=[CH:21][CH:22]=3)[CH:17]=[C:16]2[CH2:30][CH2:31][CH3:32])[N:10]=1

参加物

5

反応条件

温度
70 °C

実験手順

A solution containing 1-{[5-(2-chloro-5-iodophenyl)-1,2,4-oxadiazol-3-yl]methyl}-2-propyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile (Example 291) (0.378 g, 0.662 mmol), 1,1-bisdiphenylphosphinoferrocene (0.073 g, 0.132 mmol), E3N (1.0 mL, 13.6 mmol), Pd(OAc)2 (0.032 g, 0.132 mmol), anhydrous MeOH (2.0 mL) and anhydrous DMF (20 mL). The mixture was then stirred at 70° C. under a carbon monoxide atmosphere for a period of 4 h and then allowed to cooled to rt. The reaction was partitioned between NaHCO3 and EtOAc, dried (MgSO4) and concentrated to dryness. The mixture was purified on a biotage prepak column (0-10% EtOAc-hexanes gradient) to give 0.214 g (64% yield) of pure product: MS (ES) m/z 502 (M+).

後処理

  1. temperatureto cooled to rt
  2. customThe reaction was partitioned between NaHCO3 and EtOAc
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated to dryness
  5. customThe mixture was purified on a biotage prepak column (0-10% EtOAc-hexanes gradient)

出典と根拠

ORDレコード
ord-c8a37e7d0f7244bea4fc1a09eef90d40
出典データセット
uspto-grants-2009_08
特許番号
US07572820B2

反応ノート

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