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Methyl iodide → HCID 178503083, 화합물

HRID 1471854
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HRID 1471854 반응식
[C:1]([C:4]1C=CC=[CH:6][CH:5]=1)(=O)[CH3:2].[C:10](=[S:12])=S.[H-].[Na+].IC.[NH2:17][NH2:18].[CH2:19]1[CH2:23]O[CH2:21][CH2:20]1>>[CH3:10][S:12][C:21]1[NH:18][N:17]=[C:19]([C:23]2[CH:6]=[CH:5][CH:4]=[CH:1][CH:2]=2)[CH:20]=1
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참가 물질

7

반응물 6

HCID 6328Methyl iodideHCID 6348Carbon DisulfideHCID 7410AcetophenoneHCID 8028TetrahydrofuranHCID 9321HydrazineHCID 24758Sodium hydride

생성물 1

HCID 178503083HCID 178503083, 화합물

실험 절차

To a solution of acetophenone (5.0 g, 41.6 mmol) and CS2 (3.17 g, 41.6 mmol) in THF (150 mL) was added sodium hydride (1.997 g, 83 mmol) at 0° C. After 30 min at 0° C., the reaction was warmed to room temperature and stirred for 1 h, then refluxed for 4 h. The reaction was cooled to room temperature, added iodomethane (16.23 g, 104 mmol), and refluxed for another 12 h. The reaction was cooled and extracted with ethyl acetate. The organic extracts were concentrated under reduced pressure. The residue was diluted with ethanol (200 mL), added hydrazine (1.334 g, 41.6 mmol), and refluxed for 4 h. After cooling, the mixture was concentrated under reduced pressure and extracted with ethyl acetate. The organic extracts were dried over MgSO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (6.02 g). LCMS m/z=191.37 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 2.31 (s, 3H), 6.21 (s, 1H), 7.38-7.56 (m, 5H), 12.2 (s, 1H).

후처리

  1. temperaturerefluxed for 4 h
  2. temperatureThe reaction was cooled to room temperature
  3. temperaturerefluxed for another 12 h
  4. temperatureThe reaction was cooled
  5. extractionextracted with ethyl acetate
  6. concentrationThe organic extracts were concentrated under reduced pressure
  7. additionThe residue was diluted with ethanol (200 mL)
  8. temperaturerefluxed for 4 h
  9. temperatureAfter cooling
  10. concentrationthe mixture was concentrated under reduced pressure
  11. extractionextracted with ethyl acetate
  12. dry with materialThe organic extracts were dried over MgSO4
  13. concentrationconcentrated under reduced pressure
  14. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-fd5815c9d858487d939490a379418faf
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012478B2

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