Potassium Carbonate → ethyl 1-(3-chloropyridin-2-yl)-3-{[5-(trifluoromethyl)-2H-tetrazol-2-yl]acetyl}-1H-pyrazole-5-carboxylate

HRID 1630662Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1630662
[F:1][C:2]([F:9])([F:8])[C:3]1[N:4]=[N:5][NH:6][N:7]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:17][C:18]([C:20]1[CH:24]=[C:23]([C:25]([O:27][CH2:28][CH3:29])=[O:26])[N:22]([C:30]2[C:35]([Cl:36])=[CH:34][CH:33]=[CH:32][N:31]=2)[N:21]=1)=[O:19]>C(#N)C>[Cl:36][C:35]1[C:30]([N:22]2[C:23]([C:25]([O:27][CH2:28][CH3:29])=[O:26])=[CH:24][C:20]([C:18](=[O:19])[CH2:17][N:5]3[N:6]=[N:7][C:3]([C:2]([F:9])([F:8])[F:1])=[N:4]3)=[N:21]2)=[N:31][CH:32]=[CH:33][CH:34]=1

Komponenten

5

Versuchsvorschrift

1.24 g (2.04 mmol) of 5-(trifluoromethyl)-2H-tetrazole and 348 mg (2.52 mmol) of potassium carbonate were initially charged in 15 ml of acetonitrile and stirred at RT for 15 min. 693 mg (1.57 mmol) of ethyl 3-(bromoacetyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate, dissolved in 5 ml of acetonitrile, were added, and the reaction mixture was stirred at 70° C. for 5 min. Half of the solvent was distilled off, the residue was diluted with 80 ml of water and the mixture was extracted twice with dichloromethane. The combined organic phases are washed with sodium chloride solution, dried over sodium sulphate and concentrated. The desired product was isolated by chromatographic purification.

Aufarbeitung

  1. additionwere added
  2. stirringthe reaction mixture was stirred at 70° C. for 5 min
  3. distillationHalf of the solvent was distilled off
  4. additionthe residue was diluted with 80 ml of water
  5. extractionthe mixture was extracted twice with dichloromethane
  6. washThe combined organic phases are washed with sodium chloride solution
  7. dry with materialdried over sodium sulphate
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-9553a1d4656444319cf12a01fec40b95
Quelldatensatz
uspto-grants-2014_07
Patentnummer
US08791139B2

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