Methanol → 2-(5-Methoxy-7-methyl-1H-indol-4-yl)acetonitrile

HRID 2174126노트

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HRID 2174126 반응식
CC([O-])(C)C.[K+].CC1C=CC(S([CH2:17][N+:18]#[C-])(=O)=O)=CC=1.[CH:20]([C:22]1[C:30]([O:31][CH3:32])=[CH:29][C:28]([CH3:33])=[C:27]2[C:23]=1[CH:24]=[CH:25][N:26]2C(OC(C)(C)C)=O)=O.CO>C1COCC1>[CH3:32][O:31][C:30]1[C:22]([CH2:20][C:17]#[N:18])=[C:23]2[C:27](=[C:28]([CH3:33])[CH:29]=1)[NH:26][CH:25]=[CH:24]2

참가 물질

6

실험 절차

To a suspension of KOtBu (6.98 g, 62.2 mmol) in THF (50.0 mL) at −78° C. was added TOSMIC (8.10 g, 41.5 mmol) in THF (50.0 mL). The mixture was stirred at −78° for 15 minutes. To the mixture at −78° C. was then added a solution of tert-butyl 4-formyl-5-methoxy-7-methyl-1H-indole-1-carboxylate (Example 19-D) (6 g, 20.74 mmol) in THF (50 mL). The reaction was stirred at −78° C. for 1.5 hours. MeOH (10 ml) was then added and the reaction was removed from the dry ice bath. After 30 minutes the reaction was placed in a 40° C. water bath for 30 minutes. At this point, the reaction was cooled in an ice bath and was quenched with a saturated solution of ammonium chloride and then diluted with water and EtOAc. The layers were separated and the organics layer was dried, concentrated and absorbed onto silica to purify via FCC (0-50% EtOAc:heptanes) to afford the title compound. MS (ESI+) m/z 201.2 (M+H).

후처리

  1. stirringThe reaction was stirred at −78° C. for 1.5 hours
  2. customthe reaction was removed from the dry ice bath
  3. waitAfter 30 minutes the reaction was placed in a 40° C.
  4. waitwater bath for 30 minutes
  5. temperatureAt this point, the reaction was cooled in an ice bath
  6. customwas quenched with a saturated solution of ammonium chloride
  7. additiondiluted with water and EtOAc
  8. customThe layers were separated
  9. customthe organics layer was dried
  10. concentrationconcentrated
  11. customabsorbed onto silica
  12. customto purify via FCC (0-50% EtOAc:heptanes)

출처 및 근거

ORD 기록
ord-e70634ca42c549e2a878e33f7d282f66
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09056874B2

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