3-Hydroxypyridine → tert-Butyl 3-(pyridin-3-yloxy)pyrrolidine-1-carboxylate
Reaction equation
[C:32]([CH3:33])([CH3:34])([CH3:35])[O:36][C:37](=[O:38])[N:39]1[CH2:40][CH:41]([OH:44])[CH2:42][CH2:43]1.[CH2:52]1[O:53][CH2:54][CH2:55][CH2:56]1.[O:20]=[C:21]([O:22][CH2:23][CH3:24])[N:25]=[N:26][C:27]([O:28][CH2:29][CH3:30])=[O:31].[OH:45][c:46]1[cH:47][n:48][cH:49][cH:50][cH:51]1.[c:1]1([P:2]([c:3]2[cH:4][cH:5][cH:6][cH:7][cH:8]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][cH:14]2)[cH:15][cH:16][cH:17][cH:18][cH:19]1>>[C:32]([CH3:33])([CH3:34])([CH3:35])[O:36][C:37](=[O:38])[N:39]1[CH2:40][CH:41]([O:44][c:46]2[cH:47][n:48][cH:49][cH:50][cH:51]2)[CH2:42][CH2:43]1Participants
6
Sources & evidence
- ORD record
- ord-d150045251544f71be0f4945aa94d60e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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