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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472343Generated: October 25, 2026

3-(Methylsulfonyl)phenylboronic acid → 5-(3-(Methylsulfonyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/472343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
Reactant5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
Product5-(3-(Methylsulfonyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 5918643752%

Reaction Steps

5-(3-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine was prepared from 5-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (3.00 g, 14.0 mmol) and 3-methanesulfonyl phenyl boronic acid (3.08 g, 15.0 mmol), in a manner analogous to Step 73c. The residue was purified on a 80 g Isco silica gel column using a gradient of 0-20% methanol in dichloromethane as an eluent. 5-(3-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (2.10 g, 52%) was isolated as a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-0627770d51f641adbb8c0977df2b3c62
Source noteuspto-grants-2014_01