Dimethyl Sulfoxide → Ethyl 2-(3-nitropyridin-4-yl)acetate

HRID 2414727노트

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HRID 2414727 반응식
[CH2:1]([O:3][C:4](=[O:20])[CH:5]([C:11]1[CH:16]=[CH:15][N:14]=[CH:13][C:12]=1[N+:17]([O-:19])=[O:18])C(OCC)=O)[CH3:2].[Cl-].[Li+].O.CS(C)=O>C(OCC)(=O)C>[CH2:1]([O:3][C:4](=[O:20])[CH2:5][C:11]1[CH:16]=[CH:15][N:14]=[CH:13][C:12]=1[N+:17]([O-:19])=[O:18])[CH3:2]

참가 물질

6

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온도
100 °C

실험 절차

To a 100 ml RB flask was added 1.5 g (5.3 mmol) of 3-nitro4-pyridinyl-propanedioic acid diethyl ester, 0.450 g (10.6 mmol) of lithium chloride, 0.095 g (5.3 mmol) of water and 35 mL of DMSO. The solution was heated at 100° C. for 4 h. The cooled reaction mixture was diluted with ethyl acetate (50 mL) and washed successively with water (50 mL) and brine (50 mL). The organic phase was dried over sodium sulfate, filtered and concentrated, and the residue was chromatographed on silica gel eluting with a hexane-10% EtOAc/hexane gradient to give 0.76 g of the title compound as a yellow solid. 1H NMR (DMSO-d6): δ 1.14 (t, J=7.1 Hz, 3H), 4.06 (q, J=7.1 Hz, 2H), 4.12 (s, 2H), 7.63 (d, J=4.9 Hz, 1H), 8.82 (d, J=4.9 Hz, 1H), 9.21 (s, 1H); C9H10N2O4: APES+MS m/z 211 (M+H).

후처리

  1. customThe cooled reaction mixture
  2. washwashed successively with water (50 mL) and brine (50 mL)
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customthe residue was chromatographed on silica gel eluting with a hexane-10% EtOAc/hexane gradient

출처 및 근거

ORD 기록
ord-1c22ce7af6b941d6af528c521012d145
출처 데이터셋
uspto-grants-2004_11
특허 번호
US06815439B2

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