Methanol → Diethyl formamido[(1H-indol-3-yl)methyl]propanedioate

HRID 1390832

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HRID 1390832 반응식
[CH2:1]([O:3][C:4]([C:6]1([C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:10][CH:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N+:17]([O-])=O)[CH:8](O)[N:7]1[CH:21]=[O:22])=[O:5])[CH3:2].CO.[H][H]>[Ni].C(O)(=O)C>[CH2:1]([O:3][C:4](=[O:5])[C:6]([NH:7][CH:21]=[O:22])([C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:10][C:9]1[C:11]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:17][CH:8]=1)[CH3:2]

참가 물질

6

실험 절차

50.0 g (0.13 mol) of the compound of Example 4 in 500 ml. of methanol and 1 ml of acetic acid was hydrogenated in a rocking autoclave at room temperature and 200 psi in the presence of 6 g. of Raney nickel. After the hydrogen uptake (3 equivalents) was complete the filtered reaction mixture was concentrated in vacuo to a volume of 140 ml. Toluene (600 ml.) was added and the remaining methanol was removed by azeotropic distillation. The mixture was heated at reflux for an additional 30 minutes and then allowed to cool to room temperature. The precipitate was collected, washed with toluene and dried to yield 42.3 g (97%) of white crystals, m.p. 179-180° (lit. m.p. 179°). The analytical sample was prepared by recrystallization from ethaniol: m.p. 180-181°.

후처리

  1. customwas hydrogenated in a rocking autoclave at room temperature
  2. customthe filtered reaction mixture
  3. concentrationwas concentrated in vacuo to a volume of 140 ml
  4. additionToluene (600 ml.) was added
  5. customthe remaining methanol was removed by azeotropic distillation
  6. temperatureThe mixture was heated
  7. temperatureat reflux for an additional 30 minutes
  8. customThe precipitate was collected
  9. washwashed with toluene
  10. customdried

출처 및 근거

ORD 기록
ord-b74a3c1de5cf4d8186054f1480f7ec75
출처 데이터셋
uspto-grants-1979_02
특허 번호
US04140697

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