tert-Butanol → HCID 69458797、化合物
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C@H:8]2[O:12][C:11](=[O:13])[N:10]([C@H:14]([CH3:28])[CH2:15][C:16]3[C:24]4[C:19](=[C:20](C(O)=O)[CH:21]=[CH:22][CH:23]=4)[NH:18][CH:17]=3)[CH2:9]2)[CH:5]=[CH:6][CH:7]=1.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:36])C=CC=CC=1.C([N:48]([CH2:51]C)CC)C.[Cl-].[NH4+].[C:55]([OH:59])([CH3:58])([CH3:57])[CH3:56]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4]([C@H:8]2[O:12][C:11](=[O:13])[N:10]([C@H:14]([CH3:28])[CH2:15][C:16]3[C:24]4[C:19](=[C:20]([NH:48][C:51](=[O:36])[O:59][C:55]([CH3:58])([CH3:57])[CH3:56])[CH:21]=[CH:22][CH:23]=4)[NH:18][CH:17]=3)[CH2:9]2)[CH:5]=[CH:6][CH:7]=1参加物
実験手順
To a solution of 3-{(2R)-2-[(5R)-5-(3-chlorophenyl)-2-oxo-1,3-oxazolidin-3-yl]propyl}-1H-indole-7-carboxylic acid (504 mg, 1.26 mmol) in toluene (25 mL) and t-butyl alcohol (12.5 mL) are added diphenyl-phosphoryl azide (379 μL, 1.76 mmol) and triethylamine (245 μL, 1.76 mmol) under nitrogen atmosphere, and the mixture is stirred at room temperature for 30 minutes, and further stirred at 100° C. for 5 hours. The reaction solution is poured into a saturated aqueous ammonium chloride solution, and the mixture is extracted with ethyl acetate. The organic layer is washed with a saturated brine, and dried over anhydrous sodium sulfate. The solvent is evaporated and the obtained crude product is purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1→1:1) to give the title compound (427 mg, 72%).
後処理
- stirringfurther stirred at 100° C. for 5 hours
- extractionthe mixture is extracted with ethyl acetate
- washThe organic layer is washed with a saturated brine
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent is evaporated
- customthe obtained crude product
- customis purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1→1:1)
出典と根拠
- ORDレコード
- ord-01ae5de52fed4a508285d4def8bb0660
- 出典データセット
- uspto-grants-2007_05
- 特許番号
- US07217724B2
反応ノート
読み込み中…