Pyridine → 5-(4-Fluorophenyl)-3-(2-piperidinyl)pyridine

HRID 1489402

反応式

HRID 1489402 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.F[C:8]([F:13])(F)[C:9](O)=O>ClCCl>[F:13][C:8]1[CH:5]=[CH:4][C:3]([C:5]2[CH:4]=[C:3]([CH:2]3[CH2:3][CH2:4][CH2:5][CH2:6][NH:1]3)[CH:2]=[N:1][CH:6]=2)=[CH:2][CH:9]=1

参加物

4

反応条件

温度
25 °C

実験手順

The above-described pyridine derivative (1.25 g, 3.5 mmol) was dissolved in a mixture of dichloromethane (10 mL) and trifluoroacetic acid (10 mL) and this was stirred at 25° C. for 18 h. The solvents were removed in vacuo and the crude material dissolved in ethyl acetate (50 mL). Saturated sodium carbonate solution (30 mL) was added and the organic layer separated. The aqueous phase was extracted with two further portions of ethyl acetate (2×30 mL), the combined organic extracts washed with brine (20 mL), dried (Na2SO4) and concentrated in vacuo. The residue was chromatographed on silica gel with ethyl acetate, then methanol:ethyl acetate (1:9) as eluant to afford 5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine, 940 mg, 100%. 1H NMR (CDCl3, 300 MHz): δ 8.69 (d, J=2 Hz, 1 H), 8.55 (d, J=2 Hz, 1 H), 7.93 (t, J=2 Hz, 1 H), 7.56 (m, 2 H), 7.16 (app. tm, J=9 Hz, 2 H), 3.18 (d, J=12 Hz, 1 H), 2.83 (td, J=12, 3 Hz, 1 H), 2.61 (bs exch., 1 H), 1.92 (m, 2 H), 1.45-1.75 (m, 6 H).

後処理

  1. customThe solvents were removed in vacuo
  2. dissolutionthe crude material dissolved in ethyl acetate (50 mL)
  3. additionSaturated sodium carbonate solution (30 mL) was added
  4. customthe organic layer separated
  5. extractionThe aqueous phase was extracted with two further portions of ethyl acetate (2×30 mL)
  6. washthe combined organic extracts washed with brine (20 mL)
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in vacuo
  9. customThe residue was chromatographed on silica gel with ethyl acetate

出典と根拠

ORDレコード
ord-ed9a8965e87f4065b53ebdd07a1747f1
出典データセット
uspto-grants-1997_10
特許番号
US05677459

関連ノート

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