Methacrolein → 4-Methyl-1-(4-methylthiophenyl)-2-(4-sulfamoylphenyl)pyrrole
Reaktionsgleichung
[CH3:1][S:2][C:3]1[CH:22]=[CH:21][C:6]([NH:7][CH:8]([C:11]2[CH:16]=[CH:15][C:14]([S:17](=[O:20])(=[O:19])[NH2:18])=[CH:13][CH:12]=2)[C:9]#N)=[CH:5][CH:4]=1.O=[CH:24][C:25](=C)[CH3:26]>>[CH3:26][C:25]1[CH:9]=[C:8]([C:11]2[CH:16]=[CH:15][C:14]([S:17](=[O:20])(=[O:19])[NH2:18])=[CH:13][CH:12]=2)[N:7]([C:6]2[CH:21]=[CH:22][C:3]([S:2][CH3:1])=[CH:4][CH:5]=2)[CH:24]=1Komponenten
3
Versuchsvorschrift
Following a procedure similar to that described in Example 1(iii), but using α-(4-methylthioanilino)-α-(4-sulfamoylphenyl)acetonitrile [prepared as described in step (ii) above] and methacrolein as starting materials, the title compound was obtained as a slightly yellow powder (yield 33%), melting at 194-196° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-4471fcafcac448e6bd83f688c2503141
- Quelldatensatz
- uspto-grants-1999_06
- Patentnummer
- US05908858
Notizen zur Reaktion
Wird geladen…