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Fonazine

On the addition of ethereal hydrogen chloride to a solution of the base in isopropanol and recrystallization from anhydrous ethanol of the salt formed, there is obtained 3-dimethyl-sulfamovl-10-(2-dimethvlaminopropyl)phenthiazine hydrochloride (2.1 grams), MP 214°C with decomposition. After dissolving the product in anhydrous ethanol and adding meth-anesulfonic acid there is obtained fonazine mesylate. [Pg.700]

Dimethylsulfamoylphenthiazime Fonazine mesylate Thioproperazine Dimethyl sulfate... [Pg.1630]

Methanesulfonate, CjqH NjOjSj, dinttthothiazine mesylate, fonazine mesylate, Alius, Banistyl, Bonpac, Calsekin, Migristene, Neomestine, Promaquid, Yoristen. [Pg.661]

See other pages where Fonazine is mentioned: [Pg.699]    [Pg.699]    [Pg.1629]    [Pg.1671]    [Pg.1677]    [Pg.1679]    [Pg.1681]    [Pg.1690]    [Pg.1718]    [Pg.1724]    [Pg.1740]    [Pg.669]    [Pg.499]    [Pg.1005]    [Pg.1708]    [Pg.1708]    [Pg.1709]    [Pg.552]    [Pg.1374]    [Pg.661]    [Pg.699]    [Pg.699]    [Pg.1629]    [Pg.1671]    [Pg.1677]    [Pg.1679]    [Pg.1681]    [Pg.1690]    [Pg.1718]    [Pg.1724]   
See also in sourсe #XX -- [ Pg.669 ]



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Fonazine mesylate

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