5-Bromouracil → Urea, (2,6-difluorobenzyl)-

HRID 349290

反応式

HRID 349290 の反応式
BrC1C(=O)[NH:4][C:5](=[O:8])[NH:6]C=1.C/C(/O[Si](C)(C)C)=N\[Si](C)(C)C.[F:22][C:23]1[CH:30]=[CH:29][CH:28]=[C:27]([F:31])[C:24]=1[CH2:25]Br>ClC(Cl)C>[F:22][C:23]1[CH:30]=[CH:29][CH:28]=[C:27]([F:31])[C:24]=1[CH2:25][NH:4][C:5]([NH2:6])=[O:8]

参加物

5

反応条件

温度
80 °C

実験手順

A suspension of 5-bromouracil (18.45 g, 96.6 mmol) in 300 mL of dichloroethane was treated with N,O-bis(trimethylsilyl)acetamide (48 mL, 39.5 g, 194 mmol). The reaction mixture was heated at 80° C. for 3 hr under the nitrogen. The solution was cooled down to ambient temperature, 2,6-difluorobenzyl bromide (25 g, 120 mmol) was added and the reaction mixture was heated at 80° C. overnight under the protection of nitrogen. The reaction was cooled down, quenched with MeOH (15 mL), and partitioned between dichloromethane (500 mL) and water (250 mL). The organic layer was washed with brine, dried (sodium sulfate), and evaporated to give a solid. The crude product was triturated with ether, filtered, and washed with ether three times to give compound 1 (15.2 g, 50%) as a white solid; MS (CI) m/z 316.90, 318.90 (MH+).

後処理

  1. temperatureThe solution was cooled down to ambient temperature
  2. temperaturethe reaction mixture was heated at 80° C. overnight under the protection of nitrogen
  3. temperatureThe reaction was cooled down
  4. customquenched with MeOH (15 mL)
  5. custompartitioned between dichloromethane (500 mL) and water (250 mL)
  6. washThe organic layer was washed with brine
  7. dry with materialdried (sodium sulfate)
  8. customevaporated
  9. customto give a solid
  10. customThe crude product was triturated with ether
  11. filtrationfiltered
  12. washwashed with ether three times

出典と根拠

ORDレコード
ord-9cb07b852585438e943c26951b28e975
出典データセット
uspto-grants-2007_02
特許番号
US07179815B2

関連ノート

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