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Dimethylformamide → HCID 54373171、化合物

HRID 1388660
ノート
印刷プレビュー

反応式

HRID 1388660 の反応式
[H-].[Na+].[N:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1C1C=CC(=O)NC=1.[CH3:16][C:17]1C=CC(S(C)(=O)=O)=C[CH:22]=1.[CH3:27][N:28]([CH:30]=[O:31])[CH3:29]>>[CH3:27][N:28]1[CH:29]=[C:22]([N:3]2[CH:4]=[CH:5][N:6]=[CH:7][CH2:8]2)[CH:17]=[CH:16][C:30]1=[O:31]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6228DimethylformamideHCID 18521p-Tolyl methyl sulfoneHCID 24758Sodium hydrideHCID 233188115-(Pyrazin-2-yl)pyridin-2(1H)-one

生成物 1

HCID 54373171HCID 54373171、化合物

実験手順

Sodium hydride (0.75 g) is added to a stirred solution of 5-(2-pyrazinyl)-2(1H) pyridone (2.2 g) in DMF (150 ml). Methyl p-toluene sulfonate (4.0 g) is added to the stirred reaction mixture after 5 minutes of stirring. After 35 minutes reaction time at RT, the reaction mixture is filtered and the filtrate evaporated in vacuum. The oily solid residue is washed with ether, filtered and the dry solid treated with hot acetone. The acetone is filtered and the filtrate evaporated, yielding a solid. The ether filtrate from above is evaporated, yielding a solid which after washing with decane is combined with the acetone filtrate solid. The combined solids are recrystallized from toluene and decane (treated with charcoal and filtered while hot) resulting in the desired 1-methyl pyridone compound, M.P. 165.5°-166.5° C.

後処理

  1. customAfter 35 minutes reaction time at RT
  2. filtrationthe reaction mixture is filtered
  3. customthe filtrate evaporated in vacuum
  4. washThe oily solid residue is washed with ether
  5. filtrationfiltered
  6. additionthe dry solid treated with hot acetone
  7. filtrationThe acetone is filtered
  8. customthe filtrate evaporated
  9. customyielding a solid
  10. customThe ether filtrate from above is evaporated
  11. customyielding a solid which
  12. washafter washing with decane
  13. customThe combined solids are recrystallized from toluene and decane (treated with charcoal and filtered while hot)

出典と根拠

ORDレコード
ord-95bbd254e0324f768f2cb84dc66af11f
出典データセット
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04432979

反応ノート

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