Reaktionsgleichung
[CH3:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[CH3:11][O:12][C:13]1[CH:22]=[CH:21][CH:20]=[CH:19][C:14]=1[C:15](OC)=O.[NH2:23][NH2:24].[CH3:25]O>CC1C=CC(S(O)(=O)=O)=CC=1>[CH3:11][O:12][C:13]1[CH:22]=[CH:21][CH:20]=[CH:19][C:14]=1[C:15]1[C:1]([C:2]2[S:3][C:4]3[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=3[N:6]=2)=[CH:25][NH:24][N:23]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The title compound (430 mg) was prepared in four steps starting from 1.49 g (10 mmol) of 2-methylbenzothiazole and 1.66 g (10 mmol) of methyl 2-methoxybenzoate. After the reaction with hydrazine, the addition product was dissolved in methanol and heated to reflux with a catalytic amount of p-TSA (15 mg) for 2 hours to yield the title compound. MS (m/z, ES+): 308 (M+1, 100%). Yield=14%.
Aufarbeitung
- temperatureheated
- customto yield the title compound
Quellen und Nachweise
- ORD-Eintrag
- ord-d7164139c8c44f1997ebb671330a5343
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09434720B2
Verknüpfte Notizen
Wird geladen…