Triethylamine → 2-Cyano-4-[1-(3-methylphenyl)-3-methyl-1h-pyrazol-5-yl]pyridine

HRID 1635502노트

반응식

HRID 1635502 반응식
[C:1]([C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][N:15]=1)[CH2:6][C:7](=O)[CH2:8][C:9](=O)C)#[N:2].Cl.[CH3:17][C:18]1[CH:19]=[C:20]([NH:24][NH2:25])[CH:21]=[CH:22][CH:23]=1.C(N(CC)CC)C>C(O)C>[C:1]([C:3]1[CH:4]=[C:5]([C:6]2[N:24]([C:20]3[CH:21]=[CH:22][CH:23]=[C:18]([CH3:17])[CH:19]=3)[N:25]=[C:8]([CH3:9])[CH:7]=2)[CH:13]=[CH:14][N:15]=1)#[N:2]

참가 물질

5

실험 절차

To a mixture of 1-(2-cyanoisonicotinyl)-1,3-butanedione (1.10 g, 0.0058 mol) and 3-methylphenylhydrazine hydrochloride (0.97 g, 0.0061 mol) in 20 mL of ethanol was added triethylamine (0.85 mL, 0.0061 mol) dropwise. The reaction mixture was heated at reflux overnight (about eighteen hours). The solvent was removed and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated and the crude product was purified by chromatography on silica gel (ethyl acetate/hexane, 2:8) to give 1.30 g (87% yield) of product as a yellow solid: mp: 128-130° C.; Anal. Calc'd. for C17H14N4: C, 74.43; H, 5.14; N, 20.42. Found: C, 74.53; H, 5.22; N, 20.29.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux overnight (about eighteen hours)
  3. customThe solvent was removed
  4. customthe residue was partitioned between ethyl acetate and water
  5. washThe organic layer was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated
  9. customthe crude product was purified by chromatography on silica gel (ethyl acetate/hexane, 2:8)

출처 및 근거

ORD 기록
ord-74588d0bc7d14b129b4158508cda49ec
출처 데이터셋
uspto-grants-2003_01
특허 번호
US06509361B1

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