Reaktionsgleichung
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([NH:12][NH2:13])=[O:11])=[CH:9][C:4]=2[CH2:3][CH2:2]1.[F:14][C:15]1[CH:16]=[C:17]([CH2:21][CH2:22][C:23](O)=O)[CH:18]=[CH:19][CH:20]=1>>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]3[O:11][C:23]([CH2:22][CH2:21][C:17]4[CH:18]=[CH:19][CH:20]=[C:15]([F:14])[CH:16]=4)=[N:13][N:12]=3)=[CH:9][C:4]=2[CH2:3][CH2:2]1Komponenten
3
Versuchsvorschrift
In the same manner as in Example 14 and using 2,3-dihydro-1-benzofuran-5-carbohydrazide instead of 1H-benzotriazole-5-carbohydrazide and 3-(3-fluorophenyl)propionic acid instead of 3-(3-cyanophenyl)propionic acid, the title compound (yield 59%) was obtained as colorless crystals.
Quellen und Nachweise
- ORD-Eintrag
- ord-7071985ea8d54a5986ab828e97353e5d
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08492378B2
Verknüpfte Notizen
Wird geladen…