Water → N-[2-bromo-4-(1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)phenyl]-2-cyanoquinoline-6-carboxamide

HRID 70812Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 70812
[Br:1][C:2]1[CH:7]=[C:6]([C:8]([F:17])([C:13]([F:16])([F:15])[F:14])[C:9]([Br:12])([F:11])[F:10])[CH:5]=[C:4]([O:18][CH:19]([F:21])[F:20])[C:3]=1[NH:22][C:23]([C:25]1[CH:26]=[C:27]2[C:32](=[CH:33][CH:34]=1)[N+:31]([O-])=[CH:30][CH:29]=[CH:28]2)=[O:24].[N:36]12CCCN=C1CCCC[CH2:37]2.O.C(OCC)(=O)C>O1CCCC1>[Br:1][C:2]1[CH:7]=[C:6]([C:8]([F:17])([C:13]([F:16])([F:15])[F:14])[C:9]([Br:12])([F:11])[F:10])[CH:5]=[C:4]([O:18][CH:19]([F:21])[F:20])[C:3]=1[NH:22][C:23]([C:25]1[CH:26]=[C:27]2[C:32](=[CH:33][CH:34]=1)[N:31]=[C:30]([C:37]#[N:36])[CH:29]=[CH:28]2)=[O:24]

Komponenten

6

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

N-[2-Bromo-4-(1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)phenyl]-quinoline-6-carboxamide-1-oxide (0.41 g) was dissolved in tetrahydrofuran (50 ml), added with trimethylsilylnitrile (0.23 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.39 g), and stirred at 60° C. for 5 hours. Water was added to the reaction solution and extraction was carried out twice using ethyl acetate. The organic phases were combined and washed with water, and dried over anhydrous magnesium sulfate. The drying agent (anhydrous magnesium sulfate) was removed by filtration and the solvent was distilled off under the reduced pressure. The resulting residues were purified by column chromatography to obtain N-[2-bromo-4-(1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)phenyl]-2-cyanoquinoline-6-carboxamide (0.15 g, 36%).

Aufarbeitung

  1. washwashed with water
  2. dry with materialdried over anhydrous magnesium sulfate
  3. customThe drying agent (anhydrous magnesium sulfate) was removed by filtration
  4. distillationthe solvent was distilled off under the reduced pressure
  5. customThe resulting residues were purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-2994b6482b384f5aa110eaa53f3e1efe
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08822691B2

Notizen zur Reaktion

Wird geladen…