HCID 20184509, Verbindung → HCID 20184521, Verbindung

HRID 1380762Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1380762
[NH:1]([C:5]1[CH:26]=[CH:25][C:8]2[N:9]=[C:10]([C:12]3[CH:17]=[CH:16][C:15]([O:18][S:19]([CH3:22])(=[O:21])=[O:20])=[CH:14][C:13]=3[O:23][CH3:24])[NH:11][C:7]=2[CH:6]=1)C(C)=O>Cl>[NH2:1][C:5]1[CH:26]=[CH:25][C:8]2[N:9]=[C:10]([C:12]3[CH:17]=[CH:16][C:15]([O:18][S:19]([CH3:22])(=[O:21])=[O:20])=[CH:14][C:13]=3[O:23][CH3:24])[NH:11][C:7]=2[CH:6]=1

Komponenten

3

Edukt 1

HCID 20184509HCID 20184509, Verbindung

Produkt 1

HCID 20184521HCID 20184521, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Five grams (13.3 mmol) of 5-acetamino-2-(2'-methoxy-4'-methanesulfonyloxy-phenyl)-benzimidazole were suspended in 150 ml of concentrated hydrochloric acid and stirred at 80° C. for two hours. After cooling, the crude product precipitated was subjected to suction filtration and chromatographed on 500 gm of aluminium oxide (neutral) (eluant: methylene chloride with 2.5% ethanol).

Aufarbeitung

  1. temperatureAfter cooling
  2. customthe crude product precipitated
  3. filtrationwas subjected to suction filtration
  4. customchromatographed on 500 gm of aluminium oxide (neutral) (eluant: methylene chloride with 2.5% ethanol)

Quellen und Nachweise

ORD-Eintrag
ord-cb051754562b4ab1aab842a5ea9d7e84
Quelldatensatz
uspto-grants-1986_04
Patentnummer
US04582837

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