Sodium hydride → (5S)-3-(4-(3,6-Dihydro-2H-pyran-4-yl)-3-fluorophenyl)-5-(2-oxo-1H-pyridin-1-ylmethyl)oxazolidin-2-one

HRID 723794ノート

反応式

HRID 723794 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[H-].[Na+].[O:10]1[CH2:15][CH:14]=[C:13]([C:16]2[CH:21]=[CH:20][C:19]([N:22]3[CH2:26][C@H:25]([CH2:27]OS(C)(=O)=O)[O:24][C:23]3=[O:33])=[CH:18][C:17]=2[F:34])[CH2:12][CH2:11]1>CN(C)C=O>[O:10]1[CH2:11][CH:12]=[C:13]([C:16]2[CH:21]=[CH:20][C:19]([N:22]3[CH2:26][C@H:25]([CH2:27][N:3]4[CH:4]=[CH:5][CH:6]=[CH:7][C:2]4=[O:1])[O:24][C:23]3=[O:33])=[CH:18][C:17]=2[F:34])[CH2:14][CH2:15]1

参加物

5

反応物 3

HCID 24758Sodium hydrideHCID 213566765(R)-methanesulfonyloxymethyl 3-(4-[3,6-dihydro-(2H)-pyran-4-yl]-3-fluorophenyl)oxazolidin-2-oneHCID 178516071HCID 178516071、化合物

生成物 1

HCID 44354874(5S)-3-(4-(3,6-Dihydro-2H-pyran-4-yl)-3-fluorophenyl)-5-(2-oxo-1H-pyridin-1-ylmethyl)oxazolidin-2-one収率 28.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2-Hydroxypyridine (108 mg, 1.14 mM) was added at room temperature, under an atmosphere of nitrogen, to a stirred suspension of sodium hydride (60% dispersion in oil, 48 mg, 1.2 mM) in N,N-dimethylformamide (5 ml). The reaction was stirred for 30 minutes then (5R)-3-(4-(3,6-dihydro-2H-pyran-4-yl)-3-fluorophenyl)-5-methanesulfonyloxymethyloxazolidin-2-one (400 mg, 1.08 mM; WO 97-09328) was added in one portion. The mixture was stirred and heated at 60° for 5 hour before quenching in water (20 ml) and extracting with ethyl acetate. The extract was washed twice with water and once with saturated brine, dried (magnesium sulfate) and evaporated to an orange oil, which was purified by flash chromatography on silica, eluting with 2.5% methanol in dichloromethane to give the title compound (115 mg) as a colourless solid.

後処理

  1. stirringThe mixture was stirred
  2. temperatureheated at 60° for 5 hour
  3. custombefore quenching in water (20 ml)
  4. extractionextracting with ethyl acetate
  5. washThe extract was washed twice with water and once with saturated brine
  6. dry with materialdried (magnesium sulfate)
  7. customevaporated to an orange oil, which
  8. customwas purified by flash chromatography on silica
  9. washeluting with 2.5% methanol in dichloromethane

出典と根拠

ORDレコード
ord-4cca95dca340460f912052089e70f7ef
出典データセット
uspto-grants-2006_11
特許番号
US07141583B2

反応ノート

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