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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382810Generated: November 1, 2026

3-Aminophenylboronic acid → HCID 25213275, compound

https://huagongshe.com/reaction/2382810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminophenylboronic acidHCID 92269—
ReactantN-(6-bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)nicotinamideHCID 25212519—
ProductHCID 25213275HCID 2521327540%

Reaction Steps

The title compound was prepared following procedure described for intermediate A1 step a) but starting from N-(6-bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)nicotinamide ((B6), 75 mg; 0.24 mmol; 1.0 eq.) and 3-aminobenzeneboronic acid (64 mg; 0.47 mmol; 2.0 eq.). Purification by flash chromatography on silica (MeOH/DCM, gradient from 0:100 to 10:90) gave the title compound as a dark red solid (31 mg, 40%). HPLC, Rt: 1.07 min. (purity 96.3%). LC/MS, M+(ESI): 331.4, M−(ESI): 329.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-29ae695c9efd4fba8a5fee7185b08290
Source noteuspto-grants-2012_09