p-Toluenesulfonic acid → Sorafenib Tosylate

HRID 1913898

Reaktionsgleichung

[CH3:1][NH:2][C:3]([C:5]1[CH:6]=[C:7]([O:11][C:12]2[CH:13]=[CH:14][C:15]([NH:18][C:19]([NH:21][C:22]3[CH:23]=[CH:24][C:25]([Cl:32])=[C:26]([C:28]([F:31])([F:30])[F:29])[CH:27]=3)=[O:20])=[CH:16][CH:17]=2)[CH:8]=[CH:9][N:10]=1)=[O:4].[C:33]1([CH3:43])[CH:38]=[CH:37][C:36]([S:39]([OH:42])(=[O:41])=[O:40])=[CH:35][CH:34]=1>O>[CH3:43][C:33]1[CH:38]=[CH:37][C:36]([S:39]([OH:42])(=[O:41])=[O:40])=[CH:35][CH:34]=1.[CH3:1][NH:2][C:3]([C:5]1[CH:6]=[C:7]([O:11][C:12]2[CH:17]=[CH:16][C:15]([NH:18][C:19]([NH:21][C:22]3[CH:23]=[CH:24][C:25]([Cl:32])=[C:26]([C:28]([F:31])([F:29])[F:30])[CH:27]=3)=[O:20])=[CH:14][CH:13]=2)[CH:8]=[CH:9][N:10]=1)=[O:4]

Komponenten

Reaktionsbedingungen

Temperatur: 55 °C

Versuchsvorschrift

Sorafenib free base (2 g) was added to a solution of p-toluenesulphonic acid (1.63 g) in water (10 mL). The reaction mixture was stirred at about 55° C. for about 18 hours. The reaction mixture was filtered and dried under reduced pressure at about 50° C. for about 10 hours to 12 hours to obtain sorafenib tosylate.

Aufarbeitung

filtrationThe reaction mixture was filtered
customdried under reduced pressure at about 50° C. for about 10 hours to 12 hours

Quellen und Nachweise

ORD-Eintrag: ord-ffddedb5c1034e76855f6be048ae0b2d
Quelldatensatz: uspto-grants-2013_12
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08609854B2

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