Phosphorus oxybromide → 1-Bromo-6-(2-ethyl-6-methyl-phenoxy)-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester

HRID 409255ノート

反応式

HRID 409255 の反応式
[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10](O)[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][C:14]([O:19][C:20]1[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][C:21]=1[CH2:27][CH3:28])=[CH:13][CH:12]=2)=[O:7])[CH2:2][CH2:3][CH3:4].P(Br)(Br)([Br:32])=O>CC#N>[CH2:1]([O:5][C:6]([C:8]1[N:9]=[C:10]([Br:32])[C:11]2[C:16]([C:17]=1[OH:18])=[CH:15][C:14]([O:19][C:20]1[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][C:21]=1[CH2:27][CH3:28])=[CH:13][CH:12]=2)=[O:7])[CH2:2][CH2:3][CH3:4]

参加物

4

実験手順

A mixture of 6-(2-Ethyl-6-methyl-phenoxy)-1,4-dihydroxy-isoquinoline-3-carboxylic acid butyl ester (2.83 mmol, 1.12 g), POBr3 (11 mmol, 3.19 g), MeCN (20 mL) was refluxed gently with stirring for 1 h before it was concentrated in vacuo. The residue was dissolved in CHCl3 (50 mL). Water (10 mL) and subsequently small portions of NaHCO3 (6 g) were added with stirring. The mixture was stirred for 30 min at ambient temperature before it was filtered through a pad of celite. The filtrate was dried over MgSO4. Concentration and purification of the residue by flash column chromatography on silica gel using CH2Cl2 as the eluent gave the title compound as a tan oil (450 mg); MS-(+)-ion: M+1, 79Br/81Br=458.4 and 460.6.

後処理

  1. temperaturewas refluxed gently
  2. concentrationwas concentrated in vacuo
  3. dissolutionThe residue was dissolved in CHCl3 (50 mL)
  4. additionWater (10 mL) and subsequently small portions of NaHCO3 (6 g) were added
  5. stirringwith stirring
  6. stirringThe mixture was stirred for 30 min at ambient temperature before it
  7. filtrationwas filtered through a pad of celite
  8. dry with materialThe filtrate was dried over MgSO4
  9. concentrationConcentration and purification of the residue by flash column chromatography on silica gel

出典と根拠

ORDレコード
ord-f3d9751e92d24d9faea014ba5259e3c9
出典データセット
uspto-grants-2014_06
特許番号
US08759373B2

反応ノート

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