2-Ethoxybenzoyl chloride → 2-Ethoxy-N-[3a-ethoxy-3-(2-methoxy-ethyl)-tetrahydro-furo[3,4-d]thiazol-2-ylidene]-benzamide
Reaktionsgleichung
[CH2:1]([O:3][C:4]12[CH2:11][O:10][CH2:9][CH:8]1[S:7][C:6]([NH2:12])=[N:5]2)[CH3:2].[CH2:13]([O:15][C:16]1[CH:24]=[CH:23][CH:22]=[CH:21][C:17]=1[C:18](Cl)=[O:19])[CH3:14]>>[CH2:13]([O:15][C:16]1[CH:24]=[CH:23][CH:22]=[CH:21][C:17]=1[C:18]([N:12]=[C:6]1[N:5]([CH2:2][CH2:1][O:3][CH3:4])[C:4]2([O:3][CH2:1][CH3:2])[CH2:11][O:10][CH2:9][CH:8]2[S:7]1)=[O:19])[CH3:14]Komponenten
3
Versuchsvorschrift
The product from Example 125B and 2-ethoxybenzoyl chloride were processed as described for example 118A to afford the title compound. MS (ESI+) m/z 395 (M+H)+.
Quellen und Nachweise
- ORD-Eintrag
- ord-84d87c592b8a4e1a946e58405e41dde9
- Quelldatensatz
- uspto-grants-2014_09