1-Bromo-3-methylbutane → 4-[1-(3-Methyl-butyl)-6-nitro-1H-indol-3-yl]-benzonitrile

HRID 2079896

反応式

HRID 2079896 の反応式
C([O-])([O-])=O.[Cs+].[Cs+].[N+:7]([C:10]1[CH:18]=[C:17]2[C:13]([C:14]([C:19]3[CH:26]=[CH:25][C:22]([C:23]#[N:24])=[CH:21][CH:20]=3)=[CH:15][NH:16]2)=[CH:12][CH:11]=1)([O-:9])=[O:8].[CH2:27](Br)[CH2:28][CH:29]([CH3:31])[CH3:30]>CN(C=O)C>[CH3:30][CH:29]([CH3:31])[CH2:28][CH2:27][N:16]1[C:17]2[C:13](=[CH:12][CH:11]=[C:10]([N+:7]([O-:9])=[O:8])[CH:18]=2)[C:14]([C:19]2[CH:20]=[CH:21][C:22]([C:23]#[N:24])=[CH:25][CH:26]=2)=[CH:15]1

参加物

5

反応物 3

HCID 78911-Bromo-3-methylbutaneHCID 10796Cesium carbonateHCID 574421974-(6-nitro-1H-indol-3-yl)-benzonitrile

生成物 1

HCID 574421904-[1-(3-Methyl-butyl)-6-nitro-1H-indol-3-yl]-benzonitrile収率 95%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Method L Add Cs2CO3 (1.0 g, 1.88 mmol) to a solution of 4-(6-Nitro-1H-indol-3-yl)-benzonitrile, 9, (100 mg, 0.37 mmol) and isopentyl bromide (0.1 mL, 0.75 mmol) in DMF (10 mL). Stir overnight at ambient temperature. Remove the DMF solvent to provide a solid and partition the solid between EtOAc and H2O, Sequentially wash the organic layer with H2O and brine then dry the organic layer over MgSO4. Filter and remove the solvent leaving a solid. Purify by silica gel column chromatography (0-100% EtOAc/hexanes gradient) and concentrated to dryness to afford 180 mg (95%) of the title compound. LRMS (API ES+)=334.3 (M+H).

後処理

  1. customRemove the DMF solvent
  2. customto provide a solid
  3. custompartition the solid between EtOAc and H2O
  4. washSequentially wash the organic layer with H2O and brine
  5. dry with materialthen dry the organic layer over MgSO4
  6. filtrationFilter
  7. customremove the solvent
  8. customleaving a solid
  9. customPurify by silica gel column chromatography (0-100% EtOAc/hexanes gradient)
  10. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-55ac11c51faa4283ae924097c48e9388
出典データセット
uspto-grants-2011_04
特許番号
US07932284B2

関連ノート

読み込み中…