HCID 3803, Verbindung → HCID 15022009, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:12]=[C:11]2[C:5]([C:6]([Cl:15])=[C:7]([O:13][CH3:14])[O:8][C:9]2=[O:10])=[CH:4][CH:3]=1.[C:16]1([N:22]=[C:23]=[O:24])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(Cl)Cl>[C:16]1([NH:22][C:23]([NH:1][C:2]2[CH:12]=[C:11]3[C:5]([C:6]([Cl:15])=[C:7]([O:13][CH3:14])[O:8][C:9]3=[O:10])=[CH:4][CH:3]=2)=[O:24])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This compound was prepared by reaction of 110 mg (0.5 mmol) of 7-amino-4-chloro-3-methoxyisocoumarin with 60 mg (0.5 mmol) of phenyl isocyanate at room temperature in CH2Cl2 for 24 h. After standard work-up, this isocoumarin was obtained as yellow crystals; mp 203°-204° C.; MS, m/e 344 (M+). Anal. Calc. for C17H13ClN2O4 : C, 59.23; H, 3.08; N, 8.13; Cl, 10.28. Found: C, 59.28; H, 3.82; N, 8.11; Cl, 10.35.