2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-Acetyl-7-(benzyloxy)quinolin-2(1H)-one

HRID 33381ノート

反応式

HRID 33381 の反応式
[C:1]([C:4]1[CH:13]=[C:12]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][C:8](=[O:22])[NH:9]2)(=[O:3])[CH3:2].ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>O1CCOCC1>[C:1]([C:4]1[CH:13]=[C:12]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:22])[NH:9]2)(=[O:3])[CH3:2]

参加物

4

実験手順

13.0 g (44 mmol) 5-acetyl-7-benzyloxy-3,4-dihydro-1H-quinolin-2-one are suspended in 130 mL dioxane and combined with 15.0 g (66 mmol) of 2,3-dichloro-5,6-dicyanobenzoquinone. The mixture is refluxed for 30 minutes, cooled to ambient temperature and stirred for a further 2 hours. The solid is filtered off, washed with dioxane and dissolved in 600 mL dichloromethane/methanol (9:1). The solution is washed with sodium hydrogen carbonate solution, dried with sodium sulphate and evaporated down. Then the residue is suspended in methanol, filtered and dried.

後処理

  1. temperatureThe mixture is refluxed for 30 minutes
  2. filtrationThe solid is filtered off
  3. washwashed with dioxane
  4. dissolutiondissolved in 600 mL dichloromethane/methanol (9:1)
  5. washThe solution is washed with sodium hydrogen carbonate solution
  6. dry with materialdried with sodium sulphate
  7. customevaporated down
  8. filtrationfiltered
  9. customdried

出典と根拠

ORDレコード
ord-77418d8c43974fee8734f31649c38fcb
出典データセット
uspto-grants-2008_09
特許番号
US07429583B2

反応ノート

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