Acetic Acid → 1-Ethyl-3-cyano-5,6-dimethyl-2-pyridone

HRID 489277노트

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HRID 489277 반응식
[Na].[CH3:2][CH:3]([C:6](=O)[CH3:7])[CH:4]=O.[CH2:9]([NH:11][C:12](=[O:16])[CH2:13][C:14]#[N:15])[CH3:10].C(O)(=O)C.N1CCCCC1>CN(C=O)C.C(Cl)(Cl)Cl>[CH2:9]([N:11]1[C:6]([CH3:7])=[C:3]([CH3:4])[CH:2]=[C:13]([C:14]#[N:15])[C:12]1=[O:16])[CH3:10]

참가 물질

7

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온도
135 °C

실험 절차

To a suspension of 2-methyl-3-oxobutanal sodium salt (3.18 g) and N-ethylcyanoacetamide (3-0003-02) (2.243 g) in DMF (20 mL) were added acetic acid (1.49 mL) and piperidine (0.40 mL) at room temperature, and the reaction mixture was refluxed with stirring in an oil bath at 135° C. for 5 h. The reaction mixture was dissolved in chloroform and water, extracted three times with chloroform, dried over magnesium sulfate, and evaporated under reduced pressure. The obtained crystal residue (4.07 g) was washed three times with n-hexane (1 mL) to give 1-ethyl-3-cyano-5,6-dimethyl-2-pyridone (3-003-03) (3.38 g, 96%) as a brown crystal.

후처리

  1. temperaturethe reaction mixture was refluxed
  2. extractionwater, extracted three times with chloroform
  3. dry with materialdried over magnesium sulfate
  4. customevaporated under reduced pressure
  5. washThe obtained crystal residue (4.07 g) was washed three times with n-hexane (1 mL)

출처 및 근거

ORD 기록
ord-b4f7396f593b4a43960e0acfe266bdbd
출처 데이터셋
uspto-grants-2005_12
특허 번호
US06977266B2

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