Sodium Iodide → N-(3,5-dibromopyrazin-2-yl)-2-iodoacetamide

HRID 717135ノート

反応式

HRID 717135 の反応式
Cl[CH2:2][C:3]([NH:5][C:6]1[C:11]([Br:12])=[N:10][C:9]([Br:13])=[CH:8][N:7]=1)=[O:4].[I-:14].[Na+]>CC(C)=O.C(OCC)(=O)C>[Br:12][C:11]1[C:6]([NH:5][C:3](=[O:4])[CH2:2][I:14])=[N:7][CH:8]=[C:9]([Br:13])[N:10]=1

参加物

5

実験手順

To a solution of 2-chloro-N-(3,5-dibromopyrazin-2-yl)acetamide (3.0 g, 9.11 mmol) in acetone (40 mL) was added sodium iodide (13.65 g, 91 mmol) dissolved in acetone (20 mL). Solution was allowed to stir at ambient temperature for 16 h. Solution was condensed under reduced pressure and diluted with ethyl acetate (500 mL) and washed consecutively with water (5×) to remove the blue color. Organics were dried over magnesium sulfate, filtered and solvent removed under reduced pressure to afford the crude product. The solid was diluted with 10% ethyl acetate in hexanes (40 mL) and sonicated while scraping the sides of the flask. The solution was then heated under a heat gun for 5 min, then cooled while sonicating at ambient temperature. The resulting solid was filtered and washed with additional hexanes and dried under vacuum to afford the title compound (3.0 g, 7.13 mmol, 78% yield). MS (ESI) m/z 420.3 [M−1]+, 422.0 [M+1]+, 424.0 [M+3]+.

後処理

  1. customcondensed under reduced pressure
  2. washwashed consecutively with water (5×)
  3. customto remove the blue color
  4. dry with materialOrganics were dried over magnesium sulfate
  5. filtrationfiltered
  6. customsolvent removed under reduced pressure
  7. customto afford the crude product
  8. customsonicated
  9. temperatureThe solution was then heated under a heat gun for 5 min
  10. temperaturecooled
  11. customwhile sonicating at ambient temperature
  12. filtrationThe resulting solid was filtered
  13. washwashed with additional hexanes
  14. customdried under vacuum

出典と根拠

ORDレコード
ord-408a8fe6b58349a49502202709e12e28
出典データセット
uspto-grants-2015_11
特許番号
US09193692B2

反応ノート

読み込み中…