Ether, bis(1-chloroethyl) → 6-Chloro-5-methoxymethoxy-nicotinonitrile

HRID 1483732

반응식

HRID 1483732 반응식
[Cl:1][C:2]1[C:9]([OH:10])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][N:3]=1.C(N(CC)C(C)C)(C)C.Cl[CH:21]([O:23][CH:24](C)Cl)C>C(Cl)Cl>[Cl:1][C:2]1[C:9]([O:10][CH2:21][O:23][CH3:24])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][N:3]=1

참가 물질

5

실험 절차

To a solution of 6-chloro-5-hydroxy-nicotinonitrile (1.12 g, 7.24 mmol) in DCM (15 mL) was added N,N-diisopropyl ethylamine (1.57 mL, 9.05 mmol) followed by the addition of chloro-methyl methylether (0.66 mL, 8.69 mmol) slowly at 0° C. After overnight at room temperature, the reaction mixture was washed with saturated NaHCO3 (10 mL) and brine (10 mL), dried over Na2SO4, filtered, and concentrated to give yellow oil. Purification was accomplished by flash chromatography on silica gel using 5-25% EtOAc/hexanes gradient elution to yield the title compound (0.68 g, 50%) as a transparent oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.53 (d, J=2.0 Hz, 1H), 8.14 (d, J=2.0 Hz, 1H), 5.42 (s, 2H), 3.40 (s, 3H); MS (ES) m/z: 199 (M+1)+.

후처리

  1. washthe reaction mixture was washed with saturated NaHCO3 (10 mL) and brine (10 mL)
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customto give yellow oil
  6. customPurification
  7. washwas accomplished by flash chromatography on silica gel using 5-25% EtOAc/hexanes gradient elution

출처 및 근거

ORD 기록
ord-e0d1dfe446ee40ada479bcd9fc7d1703
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09416146B2

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