HCID 18433362, Verbindung → HCID 9912048, Verbindung
Reaktionsgleichung
C[O:2][C:3](=[O:15])[CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[C:12]([NH2:14])[CH:11]=[CH:10][CH:9]=1.CO[C:18](=[O:38])[CH:19]([C:21]1[CH:26]=[CH:25][C:24]([N+:27]([O-])=O)=[C:23]([O:30][CH2:31]C2C=CC=CC=2)[CH:22]=1)[CH3:20]>>[NH:14]([C:31]1[O:30][C:23]2[CH:22]=[C:21]([CH:19]([C:18]([NH:14][C:12]3[CH:11]=[CH:10][CH:9]=[C:8]([O:7][CH2:6][CH2:5][CH2:4][C:3]([OH:2])=[O:15])[CH:13]=3)=[O:38])[CH3:20])[CH:26]=[CH:25][C:24]=2[N:27]=1)[C:12]1[CH:13]=[CH:8][CH:9]=[CH:10][CH:11]=1Komponenten
3
Versuchsvorschrift
Methyl4-(5-aminophenoxy)butyrate was made as described in example 7 above and coupled with methyl-2-(3-benzyloxy-4-nitrophenyl)propionate according to the method described in example 7 to produce the methyl ester of 2-anilino-6-(1-(3-[3-carboxypropoxy]anilino carbonyl)ethyl)benzoxazole.
Quellen und Nachweise
- ORD-Eintrag
- ord-3847fffce1af4927b6e18fc4da54fe1d
- Quelldatensatz
- uspto-grants-2002_08
- Patentnummer
- US06441012B1