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Sodium hydride → N-(5R)-[3-(3-Fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]N-isoxazol-3-yl-carbamic acid tert-butyl ester

HRID 747215
ノート
印刷プレビュー

反応式

HRID 747215 の反応式
[H-].[Na+].[C:3]([O:7][C:8](=[O:15])[NH:9][C:10]1[CH:14]=[CH:13][O:12][N:11]=1)([CH3:6])([CH3:5])[CH3:4].[F:16][C:17]1[CH:18]=[C:19]([N:24]2[CH2:28][C@H:27]([CH2:29]OS(C)(=O)=O)[O:26][C:25]2=[O:35])[CH:20]=[CH:21][C:22]=1[I:23]>CN(C)C=O.C(=O)(O)[O-].[Na+]>[C:3]([O:7][C:8](=[O:15])[N:9]([CH2:29][C@@H:27]1[O:26][C:25](=[O:35])[N:24]([C:19]2[CH:20]=[CH:21][C:22]([I:23])=[C:17]([F:16])[CH:18]=2)[CH2:28]1)[C:10]1[CH:14]=[CH:13][O:12][N:11]=1)([CH3:6])([CH3:4])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 24758Sodium hydrideHCID 21992950tert-Butyl 1,2-oxazol-3-ylcarbamateHCID 23624705Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

生成物 1

HCID 59749411N-(5R)-[3-(3-Fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]N-isoxazol-3-yl-carbamic acid tert-butyl ester収率 57.1%

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
3 回
HCID 516892Sodium Bicarbonate溶媒

実験手順

To sodium hydride (60% in oil, 9.04 mM) suspended in dry N,N-dimethylformamide (10 ml) under nitrogen, N-isoxazol-3-yl-carbamic acid tert-butyl ester (1.66 g, 9.04 mM) in N,N-dimethylformamide (10 ml) was added dropwise at ambient temperature. Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester (2.5 g, 6.02 mM) in N,N-dimethylformamide (10 ml) was added slowly, and the mixture heated to 75° for 2 hours. After cooling, the mixture was diluted with aqueous sodium bicarbonate (5%, 300 ml), and extracted with ethyl acetate (3×100 ml). The organic phase was washed with water (100 ml) and brine (100 ml), dried (magnesium sulfate), evaporated and crude product purified by chromatography on a 50 g silica Mega Bond Elut® column, eluting with dichloromethane. Relevant fractions were combined to give the title compound (1.73 g).

後処理

  1. temperaturethe mixture heated to 75° for 2 hours
  2. temperatureAfter cooling
  3. extractionextracted with ethyl acetate (3×100 ml)
  4. washThe organic phase was washed with water (100 ml) and brine (100 ml)
  5. dry with materialdried (magnesium sulfate)
  6. customevaporated
  7. customcrude product purified by chromatography on a 50 g silica Mega Bond Elut® column
  8. washeluting with dichloromethane

出典と根拠

ORDレコード
ord-03a142c522a44f3d8773e3dbe0f4459b
出典データセット
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07396847B2

反応ノート

読み込み中…

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