Sodium Methoxide → 8-(Methyloxy)-2-{[(1S)-1-methylpentyl]oxy}-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine

HRID 562744ノート

反応式

HRID 562744 の反応式
[CH3:1][O-:2].[Na+].Br[C:5]1[N:6]([CH:22]2[CH2:27][CH2:26][CH2:25][CH2:24][O:23]2)[C:7]2[C:12]([N:13]=1)=[C:11]([NH2:14])[N:10]=[C:9]([O:15][C@@H:16]([CH3:21])[CH2:17][CH2:18][CH2:19][CH3:20])[N:8]=2>CO>[CH3:1][O:2][C:5]1[N:6]([CH:22]2[CH2:27][CH2:26][CH2:25][CH2:24][O:23]2)[C:7]2[C:12]([N:13]=1)=[C:11]([NH2:14])[N:10]=[C:9]([O:15][C@@H:16]([CH3:21])[CH2:17][CH2:18][CH2:19][CH3:20])[N:8]=2

参加物

4

反応物 2

HCID 10942334Sodium Methoxide2 回HCID 592526088-Bromo-2-{[(1S)-1-methylpentyl]oxy}-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine

生成物 1

HCID 592525538-(Methyloxy)-2-{[(1S)-1-methylpentyl]oxy}-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒3 回

実験手順

A solution of sodium methoxide in methanol (0.5M, 20 ml, 10 mmol) was added to a solution of 8-bromo-2-{[(1S)-1-methylpentyl]oxy}-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine (2.368 g, 5.95 mmol) in methanol (10 ml) and the mixture heated under reflux for 5 hours. More sodium methoxide in methanol (4 ml, 2 mmol) was added and the mixture refluxed for a further 2 hours and then cooled and evaporated. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The organic phase was separated, washed with saturated brine, dried over anhydrous magnesium sulphate, filtered and evaporated. The residue was dissolved in dichloromethane and purified on an aminopropyl (NH2) cartridge (100 g) using a 0-100% ethyl acetate in cyclohexane gradient over 40 mins. The appropriate fractions were combined and evaporated in vacuo to give the title compound as a white foam (1.725 g).

後処理

  1. temperaturethe mixture heated
  2. temperatureunder reflux for 5 hours
  3. temperaturethe mixture refluxed for a further 2 hours
  4. temperaturecooled
  5. customevaporated
  6. customThe residue was partitioned between ethyl acetate (100 ml) and water (100 ml)
  7. customThe organic phase was separated
  8. washwashed with saturated brine
  9. dry with materialdried over anhydrous magnesium sulphate
  10. filtrationfiltered
  11. customevaporated
  12. dissolutionThe residue was dissolved in dichloromethane
  13. custompurified on an aminopropyl (NH2) cartridge (100 g)
  14. customover 40 mins
  15. customevaporated in vacuo

出典と根拠

ORDレコード
ord-6b0ed71cb1894a3e8d9e4b70ea6fcf7c
出典データセット
uspto-grants-2011_11
特許番号
US08067426B2

反応ノート

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