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Bromine → 3-Bromo-2-ethyl-imidazo[1,2-a]pyridine

HRID 1068230
ノート
印刷プレビュー

反応式

HRID 1068230 の反応式
[CH2:1]([C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][N:6]2[CH:11]=1)[CH3:2].[Br:12]Br>CCO.O>[Br:12][C:11]1[N:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]2=[N:4][C:3]=1[CH2:1][CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24408BromineHCID 218319912-Ethylimidazo[1,2-a]pyridine

生成物 1

HCID 219127413-Bromo-2-ethyl-imidazo[1,2-a]pyridine収率 66.8%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

To a solution of 2-ethyl-imidazo[1,2-a]pyridine (2.17 g, 14.9 mmol) in EtOH (25 mL) was added Br2 (2.0 g, 12.5 mmol) in H2O (5 mL) dropwise at rt. After stirring at rt for 4 h, EtOH was evaporated under reduced pressure. The residue was basified with aqueous NaHCO3 and extracted with CH2Cl2 (3×). The organic phase was washed with brine and dried over anhydrous MgSO4. Concentration followed by flash chromatography chromatography eluting with 20% EtOAc in hexanes, followed by 50% EtOAc in hexanes afforded the title compound (1.88 g) as a viscous oil. 1H NMR (500 MHz, CDCl3): δ 1.36 (t, J=7.5 Hz, 3H), 2.83 (q, J=7.6 Hz, 2H), 6.88 (t, J=6.8 Hz, 1H), 7.20 (m, 1H), 7.55 (dd, J=8.9, 0.9 Hz, 1H), 8.05 (dd, J=6.9, 1.2 Hz, 1H).

後処理

  1. customEtOH was evaporated under reduced pressure
  2. extractionextracted with CH2Cl2 (3×)
  3. washThe organic phase was washed with brine
  4. dry with materialdried over anhydrous MgSO4
  5. concentrationConcentration
  6. washeluting with 20% EtOAc in hexanes

出典と根拠

ORDレコード
ord-a6e03872aea24589a3d57b706e9c1a4f
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06248755B1

反応ノート

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