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

HRID 2189790
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2189790
[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]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

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

Produkt 1

HCID 59316734Ethyl 3-(4-cyano-1H-indazol-1-yl)propanoateAusbeute 78,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-d4e7cdb430384005883a18b109803075
Quelldatensatz
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08324254B2

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