6-{4-[4-(4-Fluoro-3-trifluoromethyl-phenyl)-1-methyl-1H-imidazol-2-yl]-piperidin-1-yl}-5-(4-methoxy-phenyl)-pyrimidin-4-ylamine → HCID 178488751, compound
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([CH:14]3[CH2:19][CH2:18][N:17]([C:20]4N=[CH:24][N:23]=[C:22](N)[C:21]=4[C:27]4[CH:32]=[CH:31][C:30]([O:33][CH3:34])=[CH:29][CH:28]=4)[CH2:16][CH2:15]3)[N:11](C)[CH:12]=2)=[CH:4][C:3]=1[C:35]([F:38])([F:37])[F:36].Br[C:40]1C=NC=CC=1N1CCC(C2NC=C(C3C=CC=C(C(F)(F)F)C=3)N=2)CC1>>[CH3:34][O:33][C:30]1[CH:31]=[CH:32][C:27]([C:21]2[CH:22]=[N:23][CH:24]=[CH:40][C:20]=2[N:17]2[CH2:16][CH2:15][CH:14]([C:10]3[NH:11][CH:12]=[C:8]([C:5]4[CH:6]=[CH:7][CH:2]=[C:3]([C:35]([F:38])([F:36])[F:37])[CH:4]=4)[N:9]=3)[CH2:19][CH2:18]2)=[CH:28][CH:29]=1Participants
3
Procedure
The title compound was prepared in an analogous manner as 6-{4-[4-(4-Fluoro-3-trifluoromethyl-phenyl)-1-methyl-1H-imidazol-2-yl]-piperidin-1-yl}-5-(4-methoxy-phenyl)-pyrimidin-4-ylamine using 3-bromo-4-(4-{4-[3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}piperidin-1-yl)pyridine instead of 5-bromo-6-(4-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-1-methyl-1H-imidazol-2-yl}piperidin-1-yl)pyrimidin-4-amine. LC-MS: (M+1=479, obsd.=479).
Sources & evidence
- ORD record
- ord-458eef3c13f642c3954eec22bb81c37d
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09145392B2
Reaction notes
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