p-Anisoyl chloride → HCID 68806197, Verbindung
Reaktionsgleichung
[CH:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]([NH:12][OH:13])=[NH:11])[CH2:6][CH2:5]1)([CH3:3])[CH3:2].[CH3:14][O:15][C:16]1[CH:24]=[CH:23][C:19]([C:20]([Cl:22])=O)=[CH:18][CH:17]=1>>[ClH:22].[CH:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]2[N:11]=[C:20]([C:19]3[CH:23]=[CH:24][C:16]([O:15][CH3:14])=[CH:17][CH:18]=3)[O:13][N:12]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
The title compound was prepared by a similar procedure to that described in Example 56, starting from 1-isopropyl-N-hydroxypiperidine-4-carboxamidine and 4-methoxybenzoyl chloride.
Quellen und Nachweise
- ORD-Eintrag
- ord-92d06936550a49c4991752d3dddf7a17
- Quelldatensatz
- uspto-grants-2008_02
- Patentnummer
- US07332508B2
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