Benzoyl chloride → N-benzoyl-3'-amino-5-formyl-6-methoxy-biphenyl-3-sulfonamide
Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[C:4]([C:8]2[C:13]([O:14][CH3:15])=[C:12]([CH:16]=[O:17])[CH:11]=[C:10]([S:18]([NH2:21])(=[O:20])=[O:19])[CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[C:22](Cl)(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[C:22]([NH:21][S:18]([C:10]1[CH:9]=[C:8]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([NH2:1])[CH:3]=2)[C:13]([O:14][CH3:15])=[C:12]([CH:16]=[O:17])[CH:11]=1)(=[O:19])=[O:20])(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Komponenten
3
Versuchsvorschrift
Proceeding as in Reference 21, but substituting 3′-amino-5-formyl-6-methoxy-biphenyl-3-sulfonamide and benzoyl chloride, gave N-benzoyl-3′-amino-5-formyl-6-methoxy-biphenyl-3-sulfonamide.
Quellen und Nachweise
- ORD-Eintrag
- ord-6ef6df4288f947d789f5aa7e7abd450e
- Quelldatensatz
- uspto-grants-2009_01
- Patentnummer