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Cesium carbonate → Ethyl 3-(4-cyano-1H-indazol-1-yl)propanoate

HRID 2189790
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HRID 2189790 반응식
[NH:1]1[C:9]2[CH:8]=[CH:7][CH:6]=[C:5]([C:10]#[N:11])[C:4]=2[CH:3]=[N:2]1.Br[CH2:13][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16].C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C)C=O>[C:10]([C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:4]=1[CH:3]=[N:2][N:1]2[CH2:13][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])#[N:11]
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참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 68320Ethyl 3-bromopropionateHCID 247293471H-Indazole-4-carbonitrile

생성물 1

HCID 59316734Ethyl 3-(4-cyano-1H-indazol-1-yl)propanoate수율 78.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
90 °C

실험 절차

1H-indazole-4-carbonitrile (0.716 g, 5 mmol), ethyl 3-bromopropanoate (1.276 ml, 10.00 mmol) and caesium carbonate (4.90 g, 15.00 mmol) were added to N,N-dimethylformamide (DMF) (20 ml) and the mixture was was heated to 90° C. for 80 minutes. The mixture was cooled before being extracted in a mixture of ethyl acetate and water. The organic fraction was washed with 3×30 ml portions of water, dried (MgSO4), filtered and evaporated. The crude product mixture was added to a Biotage column and was eluted with ethyl acetate/petrol 1:3 to give 0.95 g of the title compound. δH (CDCl3, 400 MHz) 1.17 (3H, t), 3.01 (2H, t), 4.08 (2H, q), 4.71 (2H, t), 7.46 (1H, dd), 7.54 (1H, dd), 7.81 (1H, d), 8.21 (1H, d).

후처리

  1. temperatureThe mixture was cooled
  2. extractionbefore being extracted in a mixture of ethyl acetate and water
  3. washThe organic fraction was washed with 3×30 ml portions of water
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated
  7. additionThe crude product mixture was added to a Biotage column
  8. washwas eluted with ethyl acetate/petrol 1:3

출처 및 근거

ORD 기록
ord-d4e7cdb430384005883a18b109803075
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324254B2

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