(2-Aminopyrimidin-5-yl)boronic acid → HCID 66937268, compound
Reaction equation
[Cl:1][c:2]1[n:3][c:4]([N:23]2[CH2:24][CH2:25][O:26][CH2:27][CH2:28]2)[c:5]2[c:6]([n:7]1)[s:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][N:15]([C:18]([CH:19]([CH3:20])[OH:21])=[O:22])[CH2:16][CH2:17]1)[n:10]2.[NH2:29][c:30]1[n:31][cH:32][c:33]([B:36]([OH:37])[OH:38])[cH:34][n:35]1>>[c:2]1(-[c:33]2[cH:32][n:31][c:30]([NH2:29])[n:35][cH:34]2)[n:3][c:4]([N:23]2[CH2:24][CH2:25][O:26][CH2:27][CH2:28]2)[c:5]2[c:6]([n:7]1)[s:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][N:15]([C:18]([CH:19]([CH3:20])[OH:21])=[O:22])[CH2:16][CH2:17]1)[n:10]2Participants
3
Sources & evidence
- ORD record
- ord-dc08f5e4fcbd4dac9194f7b5cc1fcbbc
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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