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Methyl morpholine oxide → 3-bromo-N-[(2S)-2-(4-fluorophenyl)-4-oxobutyl]-N-methyl-5-(trifluoromethyl)benzamide

HRID 2063305
ノート
印刷プレビュー

反応式

HRID 2063305 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:21]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:23]=1)[C:5]([N:7]([CH2:9][C@H:10]([C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1)[CH2:11][CH:12]=C)[CH3:8])=[O:6].C[N+]1([O-])CC[O:32]CC1.OS([O-])=O.[Na+]>CC(C)=O.O.O=[Os](=O)(=O)=O>[Br:1][C:2]1[CH:3]=[C:4]([CH:21]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:23]=1)[C:5]([N:7]([CH2:9][C@H:10]([C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1)[CH2:11][CH:12]=[O:32])[CH3:8])=[O:6]
参加物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 82029Methyl morpholine oxideHCID 161193783-bromo-N-[(2S)-2-(4-fluorophenyl)pent-4-en-1-yl]-N-methyl-5-(trifluoromethyl)benzamideHCID 23665763Sodium Bisulfite

生成物 1

HCID 159506583-bromo-N-[(2S)-2-(4-fluorophenyl)-4-oxobutyl]-N-methyl-5-(trifluoromethyl)benzamide収率 92%

試薬・触媒・溶媒 3

HCID 30318
Osmium Tetroxide
触媒
HCID 180Acetone溶媒
HCID 962Water溶媒2 回

実験手順

To a solution of 3-bromo-N-[(2S)-2-(4-fluorophenyl)pent-4-en-1-yl]-N-methyl-5-(trifluoromethyl)benzamide (0.86 g, 1.9 mmol) in acetone (45 mL) were added OsO4 (2.5% in t-butyl alcohol, 0.49 mL, 0.039 mmol) and 4-methylmorpholine-4-oxide (0.41 g, 3.5 mmol). The solution was stirred under nitrogen at RT overnight and then an aqueous solution of NaHSO3 (39%, 45 mL) was added. The mixture was stirred for 2 h, diluted with water and then extracted twice with methylene chloride. The combined organic solutions were separated by means of a phase separator column and the solvent was removed by evaporation. The residue (1.08 g) was dissolved in THF (18 mL) and water (4.5 mL) and to the resultant solution was added NaIO4 (0.73 g, 3.4 mmol). The mixture was stirred under nitrogen overnight at RT. The mixture was partitioned between methylene chloride and water. The aqueous phase was extracted with methylene chloride and then the combined organic solutions were washed with brine and separated by means of a phase separator column. The solvent was removed by evaporation and there was obtained 0.78 g (90%) of the title compound. 1H NMR (500 MHz, CDCl3): 2.4-4.4 (cm, 8H), 6.8-7.8 (cm, 7H), 9.8 (s, 1H); LCMS: m/z 447 (M−1)+.

後処理

  1. stirringThe mixture was stirred for 2 h
  2. extractionextracted twice with methylene chloride
  3. customThe combined organic solutions were separated by means of a phase separator column
  4. customthe solvent was removed by evaporation
  5. dissolutionThe residue (1.08 g) was dissolved in THF (18 mL)
  6. stirringThe mixture was stirred under nitrogen overnight at RT
  7. customThe mixture was partitioned between methylene chloride and water
  8. extractionThe aqueous phase was extracted with methylene chloride
  9. washthe combined organic solutions were washed with brine
  10. customseparated by means of a phase separator column
  11. customThe solvent was removed by evaporation

出典と根拠

ORDレコード
ord-4857b15308624d2b90a24a6ab0be4e47
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08288370B2

反応ノート

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