Dimethyl Sulfate → 6-Bromo-3-methoxy-1,3-dimethylindolin-2-one

HRID 2209298

反応式

HRID 2209298 の反応式
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6](O)([CH3:12])[C:7](=[O:11])[NH:8]2)=[CH:4][CH:3]=1.[C:14](=[O:17])([O-])[O-].[Cs+].[Cs+].S(OC)(O[CH3:24])(=O)=O>C(#N)C.CN(C=O)C>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([O:17][CH3:14])([CH3:12])[C:7](=[O:11])[N:8]2[CH3:24])=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 6497Dimethyl SulfateHCID 10796Cesium carbonateHCID 665802586-Bromo-3-hydroxy-3-methylindolin-2-one

生成物 1

HCID 894719146-Bromo-3-methoxy-1,3-dimethylindolin-2-one

試薬・触媒・溶媒 1

HCID 21891449acetonitrile N,N-dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

A solution of 6-bromo-3-hydroxy-3-methylindolin-2-one 7.45 (200 mg, 0.826 mmol) in ACN/DMF (2:1, 6 mL) was cooled to 0° C. Cesium carbonate (942 mg, 2.89 mmol) and dimethyl sulfate (274 μL, 2.89 mmol) were added. The reaction was stirred at 0° C. for 90 min then at room temperature for 4 hours. The mixture was filtered over celite, concentrated and the residue was purified by flash column chromatography on silica gel to afford 6-bromo-3-methoxy-1,3-dimethylindolin-2-one 7.46. 1H NMR (400 MHz, DMSO-d6) δ 7.39-7.25 (m, 3H), 3.14 (s, 3H), 2.85 (s, 3H), 1.40 (s, 3H).

後処理

  1. waitat room temperature for 4 hours
  2. filtrationThe mixture was filtered over celite,
  3. concentrationconcentrated
  4. customthe residue was purified by flash column chromatography on silica gel

出典と根拠

ORDレコード
ord-5a5b7068e3c449e6961fb87c97327213
出典データセット
uspto-grants-2016_06
特許番号
US09376441B2

関連ノート

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