Reaktionsgleichung
[OH:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5](O)=[O:6].[CH3:12][NH:13][CH3:14]>>[OH:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([N:13]([CH3:14])[CH3:12])=[O:6]Komponenten
3
Versuchsvorschrift
The title compound was prepared from 3-hydroxy-2-methylbenzoic acid and dimethylamine, using the same method as that described for preparation 75, as a solid in 42% yield. 1H NMR(400 MHz, CDCl3) δ: 1.95(s, 3H), 2.70(s, 3H), 2.95(s, 3H), 6.55(d, 1H), 6.80 (d, 1H), 7.00(m, 1H), 9.50(s, 1H); LRMS APCI m/z 180 [M+H]+
Aufarbeitung
- customthat described for preparation 75, as a solid in 42% yield
Quellen und Nachweise
- ORD-Eintrag
- ord-4d1d089f76784bb6ad8c94fc22566581
- Quelldatensatz
- uspto-grants-2009_07
- Patentnummer
- US07557131B2
Verknüpfte Notizen
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