Potassium Carbonate → Tert-butyl 4-(2-(1-acetylindolin-5-yl)ethyl)piperazine-1-carboxylate

HRID 535648

반응식

HRID 535648 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[C:20]([N:23]1[C:31]2[C:26](=[CH:27][C:28]([C:32](=O)[CH2:33]Br)=[CH:29][CH:30]=2)[CH2:25][CH2:24]1)(=[O:22])[CH3:21]>C(#N)C>[C:20]([N:23]1[C:31]2[C:26](=[CH:27][C:28]([CH2:32][CH2:33][N:11]3[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])[CH2:9][CH2:10]3)=[CH:29][CH:30]=2)[CH2:25][CH2:24]1)(=[O:22])[CH3:21]

참가 물질

5

반응 조건

온도
70 °C

실험 절차

To a solution of piperazine-1-carboxylic acid tert-butyl ester (0.750 g, 4.03 mmol) in dry acetonitrile (20 mL) grounded potassium carbonate (0.486 mL, 8.05 mmol) was added followed by the product mixture from Example 38a (1.134 g) and the reaction was heated at 70° C. under argon over night. The acetonitrile was evaporated and DCM and water was added. The layers were separated and the aq phase was extracted with DCM (3×). The combined organic phases were dried (Na2SO4), filtered and evaporated. The crude mixture was purified by flash chromatography (heptane/EtOAc 75/25 to 0/100) to give 0.823 g (55%) of the title compound.

후처리

  1. additionwas added
  2. customThe acetonitrile was evaporated
  3. additionDCM and water was added
  4. customThe layers were separated
  5. extractionthe aq phase was extracted with DCM (3×)
  6. dry with materialThe combined organic phases were dried (Na2SO4)
  7. filtrationfiltered
  8. customevaporated
  9. customThe crude mixture was purified by flash chromatography (heptane/EtOAc 75/25 to 0/100)

출처 및 근거

ORD 기록
ord-2270defa2db742d6b09fed1e47e2d406
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08859534B2

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