3-Bromopyridine → Tert-butyl 4-(4-(1-(6-methylpyridazin-3-yl)azetidine-3-carboxamido)phenyl)piperidine-1-carboxylate
Reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[NH:8]1[CH2:11][CH:10]([C:12]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([CH:21]3[CH2:26][CH2:25][N:24]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:23][CH2:22]3)=[CH:17][CH:16]=2)=[O:13])[CH2:9]1.[NH:34]1CC(C(NC2C=CC(OC3CCN(C(OC(C)(C)C)=O)CC3)=CC=2)=O)C1>>[CH3:3][C:2]1[N:34]=[N:4][C:5]([N:8]2[CH2:11][CH:10]([C:12]([NH:14][C:15]3[CH:20]=[CH:19][C:18]([CH:21]4[CH2:22][CH2:23][N:24]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:25][CH2:26]4)=[CH:17][CH:16]=3)=[O:13])[CH2:9]2)=[CH:6][CH:7]=1Participants
4
Procedure
The title compound was prepared as described in Example 1C, substituting 3-bromo-6-methylpyridazine for 3-bromopyridine and tert-butyl 4-(4-(azetidine-3-carboxamido)phenyl)piperidine-1-carboxylate for tert-butyl 4-(4-(azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylate.
Sources & evidence
- ORD record
- ord-40e86333b31f4a0ea10755e476101fce
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975398B2
Reaction notes
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