tert-butyl 5-(2-oxopyrrolidin-1-yl)-1H-indole-1-carboxylate → tert-Butyl-4-((6-(5-(2-oxopyrrolidin-1-yl)-1H-indol-1-yl)pyridin-3-yl) oxy)piperidine-1-carboxylate
Reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([O:8][CH:9]2[CH2:14][CH2:13][N:12]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:11][CH2:10]2)=[CH:4][CH:3]=1.[O:22]=[C:23]1[CH2:27][CH2:26][CH2:25][N:24]1[C:28]1[CH:29]=[C:30]2[C:34](=[CH:35][CH:36]=1)[N:33](C(OC(C)(C)C)=O)[CH:32]=[CH:31]2>>[C:18]([O:17][C:15]([N:12]1[CH2:13][CH2:14][CH:9]([O:8][C:5]2[CH:6]=[N:7][C:2]([N:33]3[C:34]4[C:30](=[CH:29][C:28]([N:24]5[CH2:25][CH2:26][CH2:27][C:23]5=[O:22])=[CH:36][CH:35]=4)[CH:31]=[CH:32]3)=[CH:3][CH:4]=2)[CH2:10][CH2:11]1)=[O:16])([CH3:21])([CH3:20])[CH3:19]Participants
3
Procedure
The title compound was prepared by following the similar procedure as described in Example-1 using tert-butyl 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate (intermediate-6) and tert-butyl 5-(2-oxopyrrolidin-1-yl)-1H-indole-1-carboxylate (intermediate-27) (0.011 g, 6%).
Sources & evidence
- ORD record
- ord-b60a315bdd9a4f3392585efe2b42917c
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000175B2
Reaction notes
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