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Hydrochloric Acid → 1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-

HRID 274282
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 274282
[H-].[Na+].[OH:3][CH2:4][CH2:5][CH2:6][S:7]([NH2:10])(=[O:9])=[O:8].Cl[C:12]1[CH:13]=[CH:14][C:15]2[N:16]([N:18]=[CH:19][N:20]=2)[N:17]=1.Cl.[Cl-].[Na+]>CN(C)C=O>[S:7]([CH2:6][CH2:5][CH2:4][O:3][C:12]1[CH:13]=[CH:14][C:15]2[N:16]([N:18]=[CH:19][N:20]=2)[N:17]=1)(=[O:9])(=[O:8])[NH2:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 24758Sodium hydrideHCID 104869183-Hydroxypropane-1-sulfonamideHCID 112406116-Chloro-(1,2,4)triazolo(1,5-b)pyridazine

Produkt 1

HCID 30738011-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-
Ausbeute 52,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

In 12 ml of dimethylformamide was suspended 0.48 g of 60% sodium hydride in oil followed by addition of 0.835 g of 3-hydroxy-1-propanesulfonamide and the mixture was stirred under reduced pressure at room temperature for 30 minutes. Then, 0.928 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added and the mixture was further stirred at room temperature for 18 hours. Following addition of 40 ml of ice water, the reaction mixture was adjusted to pH6 with 1N-hydrochloric acid then saturated with sodium chloride. The aqueous layer was extracted with tetrahydrofuran and the extract was dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from ethyl ether. The washed crystals were recrystallized from hot methanol to provide 0.811 g of title compound. m.p. 145°-147° C.

Aufarbeitung

  1. stirringthe mixture was further stirred at room temperature for 18 hours
  2. extractionThe aqueous layer was extracted with tetrahydrofuran
  3. dry with materialthe extract was dried over magnesium sulfate
  4. distillationThe solvent was distilled off under reduced pressure
  5. customthe resulting residue was crystallized from ethyl ether
  6. customThe washed crystals were recrystallized from hot methanol

Quellen und Nachweise

ORD-Eintrag
ord-ef5441d25a9b42f7b19df8c1f2556881
Quelldatensatz
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05389633

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