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Methanol → HCID 19975240, Verbindung

HRID 1450149
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1450149
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[NH:9][S:10]([C:13]1[N:23]=[C:16]2[C:17](Cl)=[N:18][CH:19]=[C:20](Br)[N:15]2[N:14]=1)(=[O:12])=[O:11].[CH3:24][O-:25].[Na+].[CH3:27][OH:28]>C(#N)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[NH:9][S:10]([C:13]1[N:23]=[C:16]2[C:17]([O:28][CH3:27])=[N:18][CH:19]=[C:20]([O:25][CH3:24])[N:15]2[N:14]=1)(=[O:12])=[O:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887MethanolHCID 10942334Sodium MethoxideHCID 19975239HCID 19975239, Verbindung

Produkt 1

HCID 19975240HCID 19975240, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A solution of 0.42 g (0.92 mmol) of N-(2,6-dichlorophenyl)-5-bromo-8-chloro[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide in 30 mL of dry acetonitrile was combined with 2.8 mL (5.6 mmol) of a 2M solution of sodium methoxide in methanol and the mixture was warmed to 40° C. under a nitrogen atmosphere with stirring. After 24 hours, the reaction was quenched with 1 mL of glacial acetic acid and the solvent was removed under reduced pressure. The residue was extracted portionwise with up to 100mL of tetrahydrofuran and the cloudy extract obtained was filtered and concentrated by evaporation under reduced pressure. The title compound was isolated from the residue obtained by flash column chromatography on silica gel using a 2 to 10 percent ethanol/dichloromethane gradient as eluent. The title compound, which was the least polar of the three compounds present, was further purified by extraction with warm methanol and diethyl ether mixtures to obtain 46 mg (12 percent of theory) as a white powder melting above 250° C. with decomposition.

Aufarbeitung

  1. customthe reaction was quenched with 1 mL of glacial acetic acid
  2. customthe solvent was removed under reduced pressure
  3. extractionThe residue was extracted portionwise with up to 100mL of tetrahydrofuran
  4. extractionthe cloudy extract
  5. customobtained
  6. filtrationwas filtered
  7. concentrationconcentrated by evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8bf524052c9a416c9dd7af14018fc1ae
Quelldatensatz
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05602075

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