Dimethyl Sulfoxide → N-(4-Bromo-1-methylpyrazol-3-yl)-7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]-pyrimidine-2-sulfonamide

HRID 1589998Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1589998
N1C=CC=CC=1.CS(C)=O.[Cl:11][C:12]1[N:17]=[C:16]([O:18][CH3:19])[N:15]2[N:20]=[C:21]([S:23](Cl)(=[O:25])=[O:24])[N:22]=[C:14]2[CH:13]=1.[NH2:27][C:28]1[C:32]([Br:33])=[CH:31][N:30]([CH3:34])[N:29]=1>C(#N)C>[Br:33][C:32]1[C:28]([NH:27][S:23]([C:21]2[N:22]=[C:14]3[N:15]([C:16]([O:18][CH3:19])=[N:17][C:12]([Cl:11])=[CH:13]3)[N:20]=2)(=[O:25])=[O:24])=[N:29][N:30]([CH3:34])[CH:31]=1

Komponenten

6

Edukt 4

HCID 679Dimethyl SulfoxideHCID 1049PyridineHCID 27352834-bromo-1-methyl-1H-pyrazol-3-amineHCID 150036517-Chloro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonyl chloride

Produkt 1

HCID 19768914N-(4-Bromo-1-methylpyrazol-3-yl)-7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]-pyrimidine-2-sulfonamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

Pyridine (1.08 g, 8.0 mmol) and dimethyl sulfoxide (0.2 g) were added to a solution of 7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonyl chloride (1.0 g, 4.0 mmol) and 3-amino-4-bromo-1-methylpyrazole (0.70 g, 4.0 mmol) in 10 mL of acetonitrile with stirring at ambient temperature and the mixture was allowed to react overnight. The mixture was then concentrated by evaporation under reduced pressure and the residue was taken up in methylene chloride. The resulting solution was extracted with water and dried over magnesium sulfate. The volatile materials were then removed by evaporation under reduced pressure and the solid residue was extracted with diethyl ether and with water, recovered by filtration, and dried under reduced pressure to obtain 0.38 g (25 percent of theory) of the title compound as a white solid melting at 230°-232° C.

Aufarbeitung

  1. customto react overnight
  2. concentrationThe mixture was then concentrated by evaporation under reduced pressure
  3. extractionThe resulting solution was extracted with water
  4. dry with materialdried over magnesium sulfate
  5. customThe volatile materials were then removed by evaporation under reduced pressure
  6. extractionthe solid residue was extracted with diethyl ether and with water
  7. filtrationrecovered by filtration
  8. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ba3653cb416548de924fafa6dbeb8b7c
Quelldatensatz
uspto-grants-1993_04
Patentnummer
US05201938

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