Phosphorus oxychloride → (2-Chloro-6-isopropyl-3-nitro-pyridin-4-yl)-ethyl-amine

HRID 895554ノート

反応式

HRID 895554 の反応式
[CH2:1]([NH:3][C:4]1[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[NH:7][C:6](=O)[C:5]=1[N+:14]([O-:16])=[O:15])[CH3:2].O=P(Cl)(Cl)[Cl:19]>>[Cl:19][C:6]1[C:5]([N+:14]([O-:16])=[O:15])=[C:4]([NH:3][CH2:1][CH3:2])[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[N:7]=1

参加物

3

実験手順

A mixture of 4-ethylamino-6-isopropyl-3-nitro-1H-pyridin-2-one (520 mg, 2.31 mmol) in POCl3 is stirred at reflux for 1.5 h. After cooling, the solution is concentrated in vacuo. The reaction flask is then placed in an ice bath and crushed ice is added to the residue. The mixture is swirled vigorously for a few minutes and then stirred at 0° C. for 1 h. The mixture is then extracted with EtOAc. The extract is washed with additional H2O (20 mL) and brine (20 mL). The extract is dried over Na2SO4 and concentrated to afford (2-chloro-6-isopropyl-3-nitro-pyridin-4-yl)-ethyl-amine as a yellow solid. The material is sufficiently pure to be used without further purification. 1H NMR (CDCl3, 400 MHz) δ 6.62 (br, 1H), 6.44 (s, 1H), 3.31 (m, 2H), 2.91 (sept, J=6.8 Hz, 1H), 1.33 (t, J=7.4 Hz, 3H), 1.26 (d, J=6.8 Hz, 6H) ppm.

後処理

  1. temperatureat reflux for 1.5 h
  2. temperatureAfter cooling
  3. concentrationthe solution is concentrated in vacuo
  4. customThe reaction flask is then placed in an ice bath
  5. customcrushed ice
  6. additionis added to the residue
  7. waitThe mixture is swirled vigorously for a few minutes
  8. stirringstirred at 0° C. for 1 h
  9. extractionThe mixture is then extracted with EtOAc
  10. washThe extract is washed with additional H2O (20 mL) and brine (20 mL)
  11. dry with materialThe extract is dried over Na2SO4
  12. concentrationconcentrated

出典と根拠

ORDレコード
ord-4b3bbb1cdd01404ca848b95cb27d2292
出典データセット
uspto-grants-2005_07
特許番号
US06916819B2

反応ノート

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