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1-Bromo-2-methylpropane → 7-Benzyl-3-(2-methylpropyl)xanthine

HRID 323860
ノート
印刷プレビュー

反応式

HRID 323860 の反応式
[CH2:1]([N:8]1[C:16]2[C:15](=[O:17])[NH:14][C:13](=[O:18])[NH:12][C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].[CH2:21](Br)[CH:22]([CH3:24])[CH3:23]>CN(C)C=O.O.CO>[CH2:1]([N:8]1[C:16]2[C:15](=[O:17])[NH:14][C:13](=[O:18])[N:12]([CH2:21][CH:22]([CH3:24])[CH3:23])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 65551-Bromo-2-methylpropane2 回HCID 24758Sodium hydrideHCID 125005077-Benzyl-1H-purine-2,6(3H,7H)-dione

生成物 1

HCID 30174687-Benzyl-3-(2-methylpropyl)xanthine

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962Water溶媒2 回
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
50 °C

実験手順

1.5 g (6.2 mmol) of 7-benzylxanthine from stage b) were dissolved in 50 ml of dimethylformamide at 50° C. and treated in portions with 0.149 g (6.2 mmol) of sodium hydride and stirred at 50° C. for one hour. 0.67 ml (6.2 mmol) of isobutyl bromide was added dropwise and the mixture was heated to 80° C. After 5 hours, a further 0.2 ml (1.86 mmol) of isobutyl bromide was added and the mixture was stirred for a further 5 hours. 12 ml of water and 5 ml of methanol were then added, the mixture was stirred at room temperature for 2 hours, a further 60 ml of water were added and the mixture was extracted three times using methyl tert-butyl ether. The organic phases were washed with water, dried using magnesium sulfate and concentrated under reduced pressure and the residue was purified by flash chromatography on a silica gel column, dichloromethane/methanol (99/1).

後処理

  1. temperaturethe mixture was heated to 80° C
  2. waitAfter 5 hours
  3. stirringthe mixture was stirred for a further 5 hours
  4. stirringthe mixture was stirred at room temperature for 2 hours
  5. extractionthe mixture was extracted three times
  6. washThe organic phases were washed with water
  7. customdried
  8. concentrationconcentrated under reduced pressure
  9. customthe residue was purified by flash chromatography on a silica gel column, dichloromethane/methanol (99/1)

出典と根拠

ORDレコード
ord-f183b62dcadc441fb61dc8c5b086b4d8
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06214992B1

反応ノート

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