Dimethyl Sulfoxide → HCID 24948546, compound

HRID 297241Notes

Reaction equation

HRID 297241 reaction equation
[CH3:40][S:41]([CH3:42])=[O:43].[Cl:1][c:2]1[n:3][c:4]([N:24]2[CH2:25][CH2:26][O:27][CH2:28][CH2:29]2)[c:5]2[c:6]([n:7]1)[s:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][N:15]([S:18](=[O:19])(=[O:20])[CH:21]3[CH2:22][CH2:23]3)[CH2:16][CH2:17]1)[cH:10]2.[NH2:30][c:31]1[n:32][cH:33][c:34]([B:37]([OH:38])[OH:39])[cH:35][n:36]1>>[c:2]1(-[c:34]2[cH:33][n:32][c:31]([NH2:30])[n:36][cH:35]2)[n:3][c:4]([N:24]2[CH2:25][CH2:26][O:27][CH2:28][CH2:29]2)[c:5]2[c:6]([n:7]1)[s:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][N:15]([S:18](=[O:19])(=[O:20])[CH:21]3[CH2:22][CH2:23]3)[CH2:16][CH2:17]1)[cH:10]2

Participants

4

Reactant 3

HCID 679Dimethyl SulfoxideHCID 17750211(2-Aminopyrimidin-5-yl)boronic acidHCID 86619273HCID 86619273, compound

Product 1

HCID 24948546HCID 24948546, compound

Sources & evidence

ORD record
ord-12195daa5e9b401ea29122266acccc3b
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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