Sodium hydride → 5-Ethynyl-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine

HRID 1941277

반응식

HRID 1941277 반응식
O[C:2](C)(C#C)[CH2:3][C:4]1[CH:5]=[C:6]([CH:10]2[N:14]([CH3:15])[C:13](=[O:16])[CH2:12][CH2:11]2)[CH:7]=[N:8][CH:9]=1.[H-].[Na+].C1(C)C=CC=CC=1.CC(C)=O>C1(C)C=CC=CC=1>[C:3]([C:4]1[CH:5]=[C:6]([CH:10]2[N:14]([CH3:15])[C:13](=[O:16])[CH2:12][CH2:11]2)[CH:7]=[N:8][CH:9]=1)#[CH:2]

참가 물질

5

반응 조건

온도
25 °C

실험 절차

5-(2-Hydroxy-2-methyl-3-butynyl)-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine (200 mg, 0.77 mmol) was dissolved in toluene (20 mL) and catalytic sodium hydride (5 mg) was added. The solution was heated until several milliliters of toluene-acetone mixture were removed by distillation. The mixture was cooled to 25° C. and water (10 mL) and ethyl acetate (20 mL) were added. The organic phase was separated and the aqueous layer extracted with ethyl acetate (2×20 mL) and the combined organic extracts were washed with brine (10 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by silica gel column chromatography with ethyl acetate as eluant to afford 5-ethynyl-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine as a solid (125 mg, 81%). M.p. 83°-84° C.; 1H NMR (CDCl 3, 300 MHz): δ8.69 (d, J=2 Hz, 1H), 8.46 (d, J=2 Hz, 1H), 7.62 (t, J=2 Hz, 1H), 4.57 (dd, J=7, 6 Hz, 1H), 3.28 (s, 1H), 2.70 (s, 3H), 2.45-2.65 (m, 3H), 1.88 (m, 1H).

후처리

  1. customwere removed by distillation
  2. additionwater (10 mL) and ethyl acetate (20 mL) were added
  3. customThe organic phase was separated
  4. extractionthe aqueous layer extracted with ethyl acetate (2×20 mL)
  5. washthe combined organic extracts were washed with brine (10 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customThe crude product was purified by silica gel column chromatography with ethyl acetate as eluant

출처 및 근거

ORD 기록
ord-da0d03fbdf6546099d1130bf05bf3727
출처 데이터셋
uspto-grants-1997_12
특허 번호
US05703100

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