Ammonium → Tert-butyl 2-(1-((1-benzylpiperidine-4-yl)(methyl)amino)-1-oxopropane-2-yloxy)-4,6-dimethylpyrimidine-5-yl(methyl)carbamate
Reaction equation
[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[N:8]1[CH2:9][CH2:10][CH:11]([N:14]([C:15]([CH:16]([CH3:17])[O:18][c:19]2[n:20][c:21]([CH3:34])[c:22]([NH:26][C:27]([O:28][C:29]([CH3:30])([CH3:31])[CH3:32])=[O:33])[c:23]([CH3:25])[n:24]2)=[O:35])[CH3:36])[CH2:12][CH2:13]1.[CH3:37][Si:38]([N-:39][Si:40]([CH3:41])([CH3:42])[CH3:43])([CH3:44])[CH3:45].[CH3:47][I:48].[Cl-:49].[K+:46].[NH4+:50].[O:51]1[CH2:52][CH2:53][CH2:54][CH2:55]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[N:8]1[CH2:9][CH2:10][CH:11]([N:14]([C:15]([CH:16]([CH3:17])[O:18][c:19]2[n:20][c:21]([CH3:34])[c:22]([N:26]([C:27]([O:28][C:29]([CH3:30])([CH3:31])[CH3:32])=[O:33])[CH3:37])[c:23]([CH3:25])[n:24]2)=[O:35])[CH3:36])[CH2:12][CH2:13]1Participants
8
Reactant 7
Product 1
Sources & evidence
- ORD record
- ord-809ee46c122f4abf84c1098538e6c766
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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