Reaktionsgleichung
[Cl:1][C:2]1[C:8]([CH3:9])=[CH:7][CH:6]=[C:5]([Cl:10])[C:3]=1[NH2:4].[CH3:11][C:12]1[CH:17]=[C:16]([CH3:18])[N:15]=[C:14]([S:19](F)(=[O:21])=[O:20])[N:13]=1>>[Cl:1][C:2]1[C:8]([CH3:9])=[CH:7][CH:6]=[C:5]([Cl:10])[C:3]=1[NH:4][S:19]([C:14]1[N:13]=[C:12]([CH3:11])[CH:17]=[C:16]([CH3:18])[N:15]=1)(=[O:20])=[O:21]Komponenten
3
Versuchsvorschrift
This material was prepared from 2,6-dichloro-3-methylaniline and 4,6-dimethyl-2-pyrimidinesulfonyl fluoride following the general procedure described in Example 2. The desired product was isolated as a solid, m.p. 234°-235°. NMR (90 MHZ) D6 -Acetone: δ 7.4 (d, 2H), 7.3 (s, 1H), 2.5 (s, 6H) and 2.3 (s, 3H).
Quellen und Nachweise
- ORD-Eintrag
- ord-ecd2f98b80d3423c9e2f3a399d300e50
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04761173
Verknüpfte Notizen
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