Hydrazine hydrate (1:1) → HCID 178490035, 화합물

HRID 2390772노트

반응식

HRID 2390772 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:10](=O)[CH2:11][C:12]2[CH:17]=[CH:16][N:15]=[C:14]([S:18][CH3:19])[N:13]=2)[CH:6]=[C:7]([CH3:9])[CH:8]=1.COC(OC)[N:24]([CH3:26])C.O.[NH2:30]N>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:10]2[C:11]([C:12]3[CH:17]=[CH:16][N:15]=[C:14]([S:18][CH3:19])[N:13]=3)=[CH:26][NH:24][N:30]=2)[CH:6]=[C:7]([CH3:9])[CH:8]=1

참가 물질

4

반응물 3

HCID 24654Hydrazine hydrate (1:1)HCID 78373Dimethylformamide dimethyl acetalHCID 508989391-(3-Methoxy-5-methylphenyl)-2-(2-(methylthio)pyrimidin-4-yl)ethanone

생성물 1

HCID 178490035HCID 178490035, 화합물수율 78.6%

실험 절차

1-(3-Methoxy-5-methylphenyl)-2-(2-(methylthio)pyrimidin-4-yl)ethanone was heated with N,N-dimethylformamide dimethylacetal (34.46 mL, 258.6 mmol) at 90° C. for 20 hours with stirring. Excess N,N-dimethylformamide dimethylacetal was removed by vacuum distillation, and the reaction mixture was dissolved in anhydrous ethanol (55 mL). To this solution was dropwise added hydrazine hydrate (2.59 mL, 51.72 mmol), and stirred at room temperature for 12 hours. After completion of the cyclization, the solvent was removed by vacuum distillation. The concentrate was treated in water and ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate, filtered and distilled under vacuum. Purification by column chromatography gave the title compound (6.35 g, 78.6%).

후처리

  1. customExcess N,N-dimethylformamide dimethylacetal was removed by vacuum distillation
  2. dissolutionthe reaction mixture was dissolved in anhydrous ethanol (55 mL)
  3. stirringstirred at room temperature for 12 hours
  4. customAfter completion of the cyclization, the solvent was removed by vacuum distillation
  5. additionThe concentrate was treated in water
  6. dry with materialethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. distillationdistilled under vacuum
  9. customPurification by column chromatography

출처 및 근거

ORD 기록
ord-aa6270d22af2431185d5f409187206c5
출처 데이터셋
uspto-grants-2012_09
특허 번호
US08273880B2

반응 노트

불러오는 중…