2-Aminopyridine → HCID 24738180、化合物

HRID 731608

反応式

HRID 731608 の反応式
Br[CH2:2][C:3]([C:5]1[C:6]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:7][O:8][C:9]=1[CH3:10])=O.[NH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=1.C(=O)([O-])O.[Na+]>C(O)C>[CH3:10][C:9]1[O:8][N:7]=[C:6]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:5]=1[C:3]1[N:17]=[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][N:19]2[CH:2]=1

参加物

5

実験手順

A mixture of 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) and 2-aminopyridine (47 mg, 0.5 mmol) in ethanol (3.1 mL) was heated under reflux under argon for 3.5 h. Then another portion of 2-aminopyridine (24 mg, 0.25 mmol) was added and heating under reflux continued for another 1 h. The resulting mixture was then cooled to room temperature and then sodium hydrogen carbonate (63 mg, 0.75 mmol) added and the resulting mixture heated under reflux for 2 h. After cooling to room temperature, the mixture was poured onto water and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over sodium sulphate and evaporated to leave a yellow oil. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50) afforded the title compound (76 mg, 55%) which was obtained as a light yellow gum. MS: m/e=276.0 [M+H]+.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux under argon for 3.5 h
  3. temperatureheating
  4. temperatureunder reflux
  5. temperaturethe resulting mixture heated
  6. temperatureunder reflux for 2 h
  7. temperatureAfter cooling to room temperature
  8. additionthe mixture was poured onto water
  9. extractionextracted with ethyl acetate
  10. washThe combined organic layers were then washed with water and brine
  11. dry with materialdried over sodium sulphate
  12. customevaporated
  13. customto leave a yellow oil
  14. customPurification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50)

出典と根拠

ORDレコード
ord-696ff80f9aef4bb98014deb962024899
出典データセット
uspto-grants-2009_09
特許番号
US07585874B2

関連ノート

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