Phosphorus oxychloride → 3-[3-(3-Methoxypropyl)-5-(6-phenylpyridin-3-yl)-4H-1,2,4-triazol-4-yl]-2-methylbenzonitrile

HRID 1797116

Reaktionsgleichung

Reaktionsgleichung von HRID 1797116
P(Cl)(Cl)(Cl)=O.[CH3:6][O:7][CH2:8][CH2:9][CH2:10][C:11]1[N:15]([C:16]2[C:17]([CH3:25])=[C:18]([CH:22]=[CH:23][CH:24]=2)[C:19]([NH2:21])=O)[C:14]([C:26]2[CH:27]=[N:28][C:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[CH:30][CH:31]=2)=[N:13][N:12]=1>>[CH3:6][O:7][CH2:8][CH2:9][CH2:10][C:11]1[N:15]([C:16]2[C:17]([CH3:25])=[C:18]([CH:22]=[CH:23][CH:24]=2)[C:19]#[N:21])[C:14]([C:26]2[CH:27]=[N:28][C:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[CH:30][CH:31]=2)=[N:13][N:12]=1

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 220192513-[3-(3-Methoxypropyl)-5-(6-phenylpyridin-3-yl)-1,2,4-triazol-4-yl]-2-methylbenzamide

Produkt 1

HCID 102015733-[3-(3-Methoxypropyl)-5-(6-phenylpyridin-3-yl)-4H-1,2,4-triazol-4-yl]-2-methylbenzonitrileAusbeute 52,3 %

Versuchsvorschrift

Phosphorus oxychloride (8 ml) was added to 3-[3-(3-methoxypropyl)-5-(6-phenylpyridin-3-yl)-1,2,4-triazol-4-yl]-2-methylbenzamide (770 mg) prepared in the Example 4, and refluxed under heating for 3 hours. After the reaction solution was cooled to ambient temperature, the solution was concentrated under reduced pressure. Chloroform was added to the resulting residue, which was then washed with saturated aqueous sodium hydrogen carbonate solution. Subsequently, the organic layer was dried over anhydrous magnesium sulfate. After the solvent was evaporated under reduced pressure, the resulting solid was recrystallized from ethyl acetate, to afford the entitled compound as white crystal (386 mg, 52%). The physico-chemical values are as follows.

Aufarbeitung

  1. customprepared in the Example 4
  2. temperaturerefluxed
  3. temperatureunder heating for 3 hours
  4. concentrationthe solution was concentrated under reduced pressure
  5. additionChloroform was added to the resulting residue, which
  6. washwas then washed with saturated aqueous sodium hydrogen carbonate solution
  7. dry with materialSubsequently, the organic layer was dried over anhydrous magnesium sulfate
  8. customAfter the solvent was evaporated under reduced pressure
  9. customthe resulting solid was recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-d5e900921ba947fea1b5b66c8001fe93
Quelldatensatz
uspto-grants-2006_04
Patentnummer
US07034047B2

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