(5-Sulfamoylpyridin-3-yl)boronic acid → HCID 57469012, compound

HRID 111986Notes

Reaction equation

HRID 111986 reaction equation
[Br:1][c:2]1[cH:3][c:4](-[c:8]2[n:9][c:10]([CH3:24])[cH:11][c:12](-[c:14]3[cH:15][cH:16][c:17]([C:20]([F:21])([F:22])[F:23])[cH:18][cH:19]3)[cH:13]2)[cH:5][cH:6][cH:7]1.[S:25]([NH2:26])(=[O:27])(=[O:28])[c:29]1[cH:30][n:31][cH:32][c:33]([B:35]([OH:36])[OH:37])[cH:34]1>>[c:2]1(-[c:33]2[cH:32][n:31][cH:30][c:29]([S:25]([NH2:26])(=[O:27])=[O:28])[cH:34]2)[cH:3][c:4](-[c:8]2[n:9][c:10]([CH3:24])[cH:11][c:12](-[c:14]3[cH:15][cH:16][c:17]([C:20]([F:21])([F:22])[F:23])[cH:18][cH:19]3)[cH:13]2)[cH:5][cH:6][cH:7]1

Participants

3

Reactant 2

HCID 57415702(5-Sulfamoylpyridin-3-yl)boronic acidHCID 574687452-(3-Bromo-phenyl)-6-methyl-4-(4-trifluoromethyl-phenyl)-pyridine

Product 1

HCID 57469012HCID 57469012, compound

Sources & evidence

ORD record
ord-8739704032b64f78b997d2f9526a5e1c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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