Acetic Anhydride → HCID 178432343, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[N:3]([CH2:16][CH:17]([CH3:19])[CH3:18])[C:4]2[N:5]([CH2:11][C:12]([CH3:15])([CH3:14])[N:13]=2)[C:6](=[O:10])[C:7]=1[N:8]=O.[C:20](OC(=O)C)(=O)[CH3:21]>>[CH3:18][CH:17]([CH3:19])[CH2:16][N:3]1[C:2]2[NH:1][C:20]([CH3:21])=[N:8][C:7]=2[C:6](=[O:10])[N:5]2[CH2:11][C:12]([CH3:15])([CH3:14])[N:13]=[C:4]12Komponenten
3
Versuchsvorschrift
The nitroso compound produced in Procedure 130 was catalytically hydrogenated and cyclized by the treatment with acetic anhydride according to the method of Procedure 63.
Quellen und Nachweise
- ORD-Eintrag
- ord-d7e813eae9e2422199c7ec8c0dadcfe4
- Quelldatensatz
- uspto-grants-1984_12
- Patentnummer
- US04489078
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