Ammonia → 4-(benzyloxy)-1-(2,3-dimethyl-2H-indazol-5-yl)pyridin-2(1H)-one

HRID 1497370Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1497370
Br[C:2]1[CH:10]=[CH:9][C:8]2[C:4](=[C:5]([CH3:12])[N:6]([CH3:11])[N:7]=2)[CH:3]=1.[CH2:13]([O:20][C:21]1[CH:26]=[CH:25][NH:24][C:23](=[O:27])[CH:22]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(=O)([O-])[O-].[K+].[K+].CNCCNC.N>CS(C)=O.[Cu]I>[CH2:13]([O:20][C:21]1[CH:26]=[CH:25][N:24]([C:2]2[CH:10]=[CH:9][C:8]3[C:4](=[C:5]([CH3:12])[N:6]([CH3:11])[N:7]=3)[CH:3]=2)[C:23](=[O:27])[CH:22]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A suspension of 5-bromo-2,3-dimethyl-2H-indazole (1.85 g), 4-(benzyloxy)pyridin-2(1H)-one (1.65 g), potassium carbonate (3.41 g), copper(I) iodide (1.57 g) and N,N′-dimethylethylenediamine (0.73 g) in DMSO (30 ml) was stirred at 150° C. for 3 hr. The reaction mixture was cooled to room temperature, and added to 28% aqueous ammonia, and the obtained precipitates were collected by filtration. The obtained solid was washed with water and diisopropyl ether, and dried under reduced pressure to give the title compound (1.85 g).

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe obtained precipitates
  3. filtrationwere collected by filtration
  4. washThe obtained solid was washed with water and diisopropyl ether
  5. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-74c313ec6f764a3b8058f3700090c7b2
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09199963B2

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