4-[1-(2-azetidin-1-yl-ethyl)-2-piperidin-4-yl-1H-imidazol-4-yl]-2-isopropyl-pyridine → HCID 118290310, compound
Reaction equation
[N:1]1([CH2:5][CH2:6][N:7]2[CH:11]=[C:10]([C:12]3[CH:17]=[CH:16][N:15]=[C:14]([CH:18]([CH3:20])[CH3:19])[CH:13]=3)[N:9]=[C:8]2[CH:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)[CH2:4][CH2:3][CH2:2]1.Cl[C:28]1[N:33]=[CH:32][N:31]=[C:30]([NH2:34])[C:29]=1[O:35][CH2:36][C:37]([F:40])([F:39])[F:38]>>[N:1]1([CH2:5][CH2:6][N:7]2[CH:11]=[C:10]([C:12]3[CH:17]=[CH:16][N:15]=[C:14]([CH:18]([CH3:20])[CH3:19])[CH:13]=3)[N:9]=[C:8]2[CH:21]2[CH2:22][CH2:23][N:24]([C:28]3[N:33]=[CH:32][N:31]=[C:30]([NH2:34])[C:29]=3[O:35][CH2:36][C:37]([F:40])([F:39])[F:38])[CH2:25][CH2:26]2)[CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
The title compound was prepared according to the procedure described for the preparation of compound “1” by using 4-[1-(2-azetidin-1-yl-ethyl)-2-piperidin-4-yl-1H -imidazol-4-yl]-2-isopropyl-pyridine and 6-chloro-5-(2,2,2-trifluoro-ethoxy)-pyrimidin-4-ylamine as the starting materials. LC-MS (M+H=545, obsd=545).
Workup
- customdescribed for the preparation of compound “1”
Sources & evidence
- ORD record
- ord-4e8bb384db7a40809af357198d9c9d37
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434714B2
Reaction notes
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