(Pyrimidin-5-yl)boronic acid → HCID 67483967, compound

HRID 2262737Notes

Reaction equation

HRID 2262737 reaction equation
Br[C:2]1[CH:3]=[C:4]([N:8]2[C:12]3[CH:13]=[CH:14][C:15]([CH:17]([N:19]4[C:27](=[O:28])[C:26]5[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=5)[C:20]4=[O:29])[CH3:18])=[CH:16][C:11]=3[N:10]=[CH:9]2)[CH:5]=[CH:6][CH:7]=1.[N:30]1[CH:35]=[C:34](B(O)O)[CH:33]=[N:32][CH:31]=1>>[N:30]1[CH:35]=[C:34]([C:2]2[CH:3]=[C:4]([N:8]3[C:12]4[CH:13]=[CH:14][C:15]([CH:17]([N:19]5[C:20](=[O:29])[C:21]6[C:26](=[CH:25][CH:24]=[CH:23][CH:22]=6)[C:27]5=[O:28])[CH3:18])=[CH:16][C:11]=4[N:10]=[CH:9]3)[CH:5]=[CH:6][CH:7]=2)[CH:33]=[N:32][CH:31]=1

Participants

3

Reactant 2

HCID 2795193(Pyrimidin-5-yl)boronic acidHCID 67484420HCID 67484420, compound

Product 1

HCID 67483967HCID 67483967, compound

Procedure

This was prepared analogously from 2-{1-[1-(3-bromo-phenyl)-1H-benzoimidazol-5-yl]-ethyl}-isoindole-1,3-dione and 5-pyrimidineboronic acid.

Sources & evidence

ORD record
ord-e3eb3fb985864c1e855e88c366bf5b84
Source dataset
uspto-grants-2010_12
Patent number
US07851490B2

Reaction notes

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