1-(2-Pyrimidinyl)piperazine → HCID 21473353, Verbindung
Reaktionsgleichung
[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([F:18])=[C:10](F)[C:11]=2[O:13][CH:14]([F:16])[F:15])[C:6](=[O:19])[C:5]2[C:20](=[O:23])[NH:21][S:22][C:4]1=2)[CH3:2].[N:24]1[CH:29]=[CH:28][CH:27]=[N:26][C:25]=1[N:30]1[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]1>>[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([F:18])=[C:10]([N:33]3[CH2:34][CH2:35][N:30]([C:25]4[N:24]=[CH:29][CH:28]=[CH:27][N:26]=4)[CH2:31][CH2:32]3)[C:11]=2[O:13][CH:14]([F:16])[F:15])[C:6](=[O:19])[C:5]2[C:20](=[O:23])[NH:21][S:22][C:4]1=2)[CH3:2]Komponenten
3
Versuchsvorschrift
The same reaction as in Example 1 was carried out by using mg (1.44 mmole) of 9-ethyl-6,7-difluoro-8-difluoromethoxy-2,3,4,9-tetrahydroisothiazolo[5,4-b]quinolin-3,4-dione and 1.9 g (11.5 mmole) of 1-(2-pyrimidinyl)piperazine to obtain 10 mg of the title compound as pale yellow powder.
Aufarbeitung
- customThe same reaction as in Example 1
Quellen und Nachweise
- ORD-Eintrag
- ord-977f321bca134b08b231176796157e05
- Quelldatensatz
- uspto-grants-1997_11
- Patentnummer
- US05688791
Notizen zur Reaktion
Wird geladen…