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

HRID 2189790
ノート
印刷プレビュー

反応式

HRID 2189790 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-d4e7cdb430384005883a18b109803075
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324254B2

反応ノート

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