(2-Aminopyrimidin-5-yl)boronic acid → HCID 24948544, compound
Reaction equation
[Cl:1][c:2]1[n:3][c:4]([N:26]2[CH2:27][CH2:28][O:29][CH2:30][CH2:31]2)[c:5]2[c:6]([n:7]1)[cH:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][CH:15]([S:18](=[O:19])(=[O:20])[c:21]3[s:22][cH:23][cH:24][n:25]3)[CH2:16][CH2:17]1)[s:10]2.[NH2:32][c:33]1[n:34][cH:35][c:36]([B:39]([OH:40])[OH:41])[cH:37][n:38]1>>[c:2]1(-[c:36]2[cH:35][n:34][c:33]([NH2:32])[n:38][cH:37]2)[n:3][c:4]([N:26]2[CH2:27][CH2:28][O:29][CH2:30][CH2:31]2)[c:5]2[c:6]([n:7]1)[cH:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][CH:15]([S:18](=[O:19])(=[O:20])[c:21]3[s:22][cH:23][cH:24][n:25]3)[CH2:16][CH2:17]1)[s:10]2Participants
3
Sources & evidence
- ORD record
- ord-43e27dc5e13041d5bda45a4347fe6d8e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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