Isonicotinic Acid → [2-(4-Fluorophenyl)-3-(4-pyridinyl)pyrazolo[1,5-a]pyridin-5-yl]methyl Isonicotinate
Reaction equation
[C:34]([P:35](=[O:36])([O:37][CH2:38][CH3:39])[O:40][CH2:41][CH3:42])#[N:43].[C:56]([O:57][CH2:58][CH3:59])(=[O:60])[CH3:61].[CH3:44][CH2:45][N:46]([CH2:47][CH3:48])[CH2:49][CH3:50].[CH3:51][N:52]([CH3:53])[CH:54]=[O:55].[CH3:62][CH2:63][CH2:64][CH2:65][CH2:66][CH3:67].[F:1][c:2]1[cH:3][cH:4][c:5](-[c:8]2[n:9][n:10]3[c:11]([cH:12][c:13]([CH2:16][OH:17])[cH:14][cH:15]3)[c:18]2-[c:19]2[cH:20][cH:21][n:22][cH:23][cH:24]2)[cH:6][cH:7]1.[n:25]1[cH:26][cH:27][c:28]([C:31](=[O:32])[OH:33])[cH:29][cH:30]1>>[F:1][c:2]1[cH:3][cH:4][c:5](-[c:8]2[n:9][n:10]3[c:11]([cH:12][c:13]([CH2:16][O:17][C:31]([c:28]4[cH:27][cH:26][n:25][cH:30][cH:29]4)=[O:32])[cH:14][cH:15]3)[c:18]2-[c:19]2[cH:20][cH:21][n:22][cH:23][cH:24]2)[cH:6][cH:7]1Participants
8
Reactant 7
Product 1
Sources & evidence
- ORD record
- ord-6ab76539fb68432c83c5d5efc1c0fd5f
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction notes
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