4-Bromo-2-methyl-quinolin-6-ol → HCID 178422415, Verbindung
Reaktionsgleichung
[C:1]([C@H:5]1[CH2:10][CH2:9][C@H:8]([O:11][C:12]2[CH:13]=[C:14]3[C:19](=[CH:20][CH:21]=2)[N:18]=[C:17]([CH3:22])[CH:16]=[C:15]3C(F)(F)F)[CH2:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2].[Br:27]C1C2C(=CC=C(O)C=2)N=C(C)C=1>>[Br:27][C:15]1[C:14]2[C:19](=[CH:20][CH:21]=[C:12]([O:11][C@H:8]3[CH2:9][CH2:10][C@H:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH2:6][CH2:7]3)[CH:13]=2)[N:18]=[C:17]([CH3:22])[CH:16]=1Komponenten
3
Versuchsvorschrift
Synthesized as per 6-(trans-4-tert-Butyl-cyclohexyloxy)-2-methyl-4-trifluoromethyl-quinoline using 4-Bromo-2-methyl-quinolin-6-ol as starting material. ESI-MS(M+H+): 378.1.
Quellen und Nachweise
- ORD-Eintrag
- ord-1b4a9e79fb754935918a82a45204008f
- Quelldatensatz
- uspto-grants-2015_11
- Patentnummer
- US09186367B2
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