Cesium fluoride → 4-[5-(1-Methyl-2-pyrrolidinyl)-3-pyridinyl]phenol

HRID 1038

반응식

HRID 1038 반응식
[Si]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:16]=[C:17]([CH:21]3[CH2:25][CH2:24][CH2:23][N:22]3[CH3:26])[CH:18]=[N:19][CH:20]=2)=[CH:11][CH:10]=1)(C(C)(C)C)(C)C.[F-].[Cs+]>CO>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([C:15]2[CH:16]=[C:17]([CH:21]3[CH2:25][CH2:24][CH2:23][N:22]3[CH3:26])[CH:18]=[N:19][CH:20]=2)=[CH:13][CH:14]=1

참가 물질

4

실험 절차

The above-described pyridine derivative (750 mg, 2.04 mmol) was dissolved in methanol (40 mL) and cesium fluoride (620 mg, 4.08 mmol) was added. The stirred mixture was heated at reflux for 18 h under inert atmosphere. After cooling the solvent was removed in vacuo and the resulting oil was dissolved in ethyl acetate (50 mL). This was washed with water (20 mL), brine (20 mL), dried (MgSO4) and concentrated. The crude material was chromatographed on "flash" silica gel with ethyl acetate:hexane (1:2 ) to 10% methanol: ethyl acetate as eluant to afford 5-(4-hydroxyphenyl)-3-(1-methyl-2-pyrrolidinyl)pyridine 480 mg, 93% as a colorless foam, 1H NMR (CDCl3, 300 MHz): δ 8.66 (d, J=2 Hz, 1 H), 8.43 (d, J=2 Hz, 1 H), 7.90 (s, 1 H), 7.32 (d, J=9 Hz, 2 H), 6.81 (d, J=9 Hz, 2 H), 3.33 (t, J=8 Hz, 1 H), 3.22 (t, J=8 Hz, 1 H), 2.41 (m, 1 H), 2.28 (s, 3 H), 2.10 (m, 2 H), 1.93 (m, 2 H).

후처리

  1. temperatureThe stirred mixture was heated
  2. temperatureat reflux for 18 h under inert atmosphere
  3. temperatureAfter cooling the solvent
  4. customwas removed in vacuo
  5. dissolutionthe resulting oil was dissolved in ethyl acetate (50 mL)
  6. washThis was washed with water (20 mL), brine (20 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. customThe crude material was chromatographed on "flash" silica gel with ethyl acetate:hexane (1:2 ) to 10% methanol

출처 및 근거

ORD 기록
ord-3d6034b340a6469bb00e1992fa10c04a
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05723477

연결된 노트

불러오는 중…