Dimethyl Sulfoxide → HCID 58234060, compound

HRID 1558433Notes

Reaction equation

HRID 1558433 reaction equation
[CH3:41][S:42]([CH3:43])=[O:44].[Cl:1][c:2]1[n:3][c:4]([N:25]2[CH2:26][CH2:27][O:28][CH2:29][CH2:30]2)[c:5]2[c:6]([n:7]1)[cH:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][C:15]([OH:18])([c:19]3[cH:20][cH:21][cH:22][cH:23][cH:24]3)[CH2:16][CH2:17]1)[s:10]2.[NH2:31][c:32]1[n:33][cH:34][c:35]([B:38]([OH:39])[OH:40])[cH:36][n:37]1>>[c:2]1(-[c:35]2[cH:34][n:33][c:32]([NH2:31])[n:37][cH:36]2)[n:3][c:4]([N:25]2[CH2:26][CH2:27][O:28][CH2:29][CH2:30]2)[c:5]2[c:6]([n:7]1)[cH:8][c:9]([CH2:11][N:12]1[CH2:13][CH2:14][C:15]([OH:18])([c:19]3[cH:20][cH:21][cH:22][cH:23][cH:24]3)[CH2:16][CH2:17]1)[s:10]2

Participants

4

Reactant 3

HCID 679Dimethyl SulfoxideHCID 17750211(2-Aminopyrimidin-5-yl)boronic acidHCID 86623539HCID 86623539, compound

Product 1

HCID 58234060HCID 58234060, compound

Sources & evidence

ORD record
ord-6fb9b169d8024a2e971ceefbe0dc4317
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

Loading…