Potassium Carbonate → 5-(2-methyl-5-nitro-1H-imidazol-1-yl)-1,6-naphthyridin-2-(1H)-one

HRID 542513ノート

反応式

HRID 542513 の反応式
Br[C:2]1[N:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](=[O:12])[NH:7]2.[CH3:13][C:14]1[NH:15][C:16]([N+:19]([O-:21])=[O:20])=[CH:17][N:18]=1.C(=O)([O-])[O-].[K+].[K+]>CN1CCCC1=O>[CH3:13][C:14]1[N:15]([C:2]2[N:11]=[CH:10][CH:9]=[C:8]3[C:3]=2[CH:4]=[CH:5][C:6](=[O:12])[NH:7]3)[C:16]([N+:19]([O-:21])=[O:20])=[CH:17][N:18]=1

参加物

5

実験手順

A mixture containing 5.6 g of 5-bromo-1,6-naphthyridin-2(1H)-one, 12.7 g of 2-methyl-5-nitro-1H-imidazole, 3.45 g of anhydrous potassium carbonate and 50 ml of N-methylpyrrolidinone was refluxed for 5.5 hours, cooled and concentrated in vacuo to remove most of the solvent. To the concentrate was added 100 ml of water and 10 ml of 35% aqueous sodium hydroxide; and, the mixture was treated with decolorizing charcoal and filtered. The filtrate was acidified with acetic acid and the precipitate was collected, washed with water, dried, recrystallized from dimethylformamide, and dried in a vacuum oven at 90°-95° C. to yield 4.5 g of 5-(2-methyl-5-nitro-1H-imidazol-1-yl)-1,6-naphthyridin-2-(1H)-one, m.p. >300° C.

後処理

  1. temperaturewas refluxed for 5.5 hours
  2. temperaturecooled
  3. concentrationconcentrated in vacuo
  4. customto remove most of the solvent
  5. additionTo the concentrate was added 100 ml of water and 10 ml of 35% aqueous sodium hydroxide
  6. additionand, the mixture was treated with decolorizing charcoal
  7. filtrationfiltered
  8. customthe precipitate was collected
  9. washwashed with water
  10. customdried
  11. customrecrystallized from dimethylformamide
  12. customdried in a vacuum oven at 90°-95° C.

出典と根拠

ORDレコード
ord-13c688ef2b4744d89847b6b5232526f1
出典データセット
uspto-grants-1987_04
特許番号
US04657915

反応ノート

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