Benzyl carbazate → benzyl 2-(1H-pyrrolo[2,3-b]pyridin-4-ylcarbonyl)hydrazinecarboxylate
Reaktionsgleichung
[NH:1]1[C:5]2[N:6]=[CH:7][CH:8]=[C:9]([C:10]([OH:12])=O)[C:4]=2[CH:3]=[CH:2]1.[C:13]([O:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(=[O:16])[NH:14][NH2:15]>>[NH:1]1[C:5]2=[N:6][CH:7]=[CH:8][C:9]([C:10]([NH:15][NH:14][C:13]([O:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[O:16])=[O:12])=[C:4]2[CH:3]=[CH:2]1Komponenten
3
Versuchsvorschrift
In the same manner as in Reference Example 1 and using 1H-pyrrolo[2,3-b]pyridine-4-carboxylic acid instead of benzothiazole-6-carboxylic acid and benzyl carbazate instead of tert-butyl carbazate, the title compound (yield 67%) was obtained as pale-yellow crystals.
Quellen und Nachweise
- ORD-Eintrag
- ord-9d70c8ca55044722a4b39326ab4ff91a
- Quelldatensatz
- uspto-grants-2013_07