2-Methyl-2-butene → 4-Iodo-2-methoxypyridine-3-carboxylic acid

HRID 457550

반응식

HRID 457550 반응식
[I:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([O:8][CH3:9])[C:3]=1[CH:10]=[O:11].CC(=CC)C.P([O-])(O)(O)=[O:18].[Na+].Cl([O-])=O.[Na+]>C(O)(C)(C)C.C1COCC1.C(O)=O.O>[I:1][C:2]1[C:3]([C:10]([OH:18])=[O:11])=[C:4]([O:8][CH3:9])[N:5]=[CH:6][CH:7]=1

참가 물질

9

실험 절차

To a solution of 4-iodo-2-methoxy-pyridine-3-carbaldehyde (4.96 g, 18.9 mmol) in 22 mL tert.-butanol was added in this order 2-methyl-2-butene (30 mL of a 2 M solution in THF, 60 mmol), natriumdihydrogen-phosphate (5.7 g, 47.5 mmol), water (15 mL) and sodiumchlorite (3.9 g, 43 mmol). The mixture was stirred at ambient temperature for 1 hour, then poured on dilute aqueous formic acid. The mixture was extracted with ethyl acetate, the organic layer washed with water and brine and concentrated. The residue was dissolved in diisopropylether+dichloromethane (1+1) and extracted 3 times with half-concentrated aqueous NaOH solution. The combined aqueous layers were acidified with conc. HCl and extracted with ethyl acetate. The organic layers were washed with water and brine, then dried over sodium sulfate and concentrated to give 3.462 g of the title compound as a white solid (67%). 1H NMR (500 MHz, CD3OD) δ 7.83 (d, J=5.4 Hz, 1H), 7.43 (d, J=5.4 Hz, 1H), 3.94 (s, 3H);

후처리

  1. extractionThe mixture was extracted with ethyl acetate
  2. washthe organic layer washed with water and brine
  3. concentrationconcentrated
  4. dissolutionThe residue was dissolved in diisopropylether+dichloromethane (1+1)
  5. extractionextracted 3 times with half-concentrated aqueous NaOH solution
  6. extractionextracted with ethyl acetate
  7. washThe organic layers were washed with water and brine
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-95f44250f2ae4abf80b18a4681f20a35
출처 데이터셋
uspto-grants-2007_03
특허 번호
US07189716B2

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