Water → 3-(3-Pyridin-2-yl-pyrazol-1-yl)-benzonitrile

HRID 2099504

반응식

HRID 2099504 반응식
[NH:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][N:7]=2)=[N:2]1.F[C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[C:16]#[N:17].C([O-])([O-])=O.[K+].[K+].O>CN(C=O)C.CCOC(C)=O>[N:7]1[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=1[C:3]1[CH:4]=[CH:5][N:1]([C:13]2[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=2)[C:16]#[N:17])[N:2]=1

참가 물질

7

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온도
145 °C

실험 절차

2-(1H-Pyrazol-3-yl)pyridine (435 mg, 3 mmol), 3-fluorobenzonitrile (0.32 mL, 3 mmol) and K2CO3 (830 mg, 6 mmol) were dissolved in DMF (10 mL) under Ar (g) and heated at 145° C. for 18 h. After cooling to ambient temperature, H2O (40 mL) and EtOAc (40 mL) were added and the reaction mixture shaken, the EtOAc layer was separated and the aqueous layer shaken with EtOAc (2×30 mL). The combined organic layers were washed with brine (3×40 mL), dried over Na2SO4 and concentrated onto silica gel. The crude material was purified by liquid chromatography on silica gel eluting with EtOAc:hexane (1:1) to afford a solid that was recrystallized from EtOAc-hexane to give 3-(3-pyridin-2-yl-1H-pyrazol-1-yl)benzonitrile as a solid. 1H NMR (CD3Cl, 300 MHz) δ 8.68-8.71 (1H, m), 8.18 (1H, m), 8.12-8.15 (1H, m), 8.02-8.06 (2H, m), 7.81 (1H, ddd), 7.60-7.62 (2H, m), 7.30 (1H, ddd), 7.20 (1H, d). MS (ESI) 247 (M+H)+

후처리

  1. temperatureAfter cooling to ambient temperature
  2. customthe EtOAc layer was separated
  3. stirringthe aqueous layer shaken with EtOAc (2×30 mL)
  4. washThe combined organic layers were washed with brine (3×40 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated onto silica gel
  7. customThe crude material was purified by liquid chromatography on silica gel eluting with EtOAc:hexane (1:1)
  8. customto afford a solid
  9. customthat was recrystallized from EtOAc-hexane

출처 및 근거

ORD 기록
ord-388019c2f29841dab091fc013b25a4f2
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07569592B2

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