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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472267Generated: October 27, 2026

3-(Methylsulfonyl)phenylboronic acid → 8-(3-(Methylsulfonyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/472267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylsulfonyl)phenylboronic acidHCID 2773542—
Reactant8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amineHCID 46864069—
Product8-(3-(Methylsulfonyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 57502374—

Reaction Steps

8-(3-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine was prepared from 8-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (1.0 g, 4.7 mmol) and 3-(methanesulfonyl)phenyl boronic acid (1.0 g, 5.0 mmol) in a manner analogous to Step 2c. The reaction product was isolated as an off-white solid (0.99 g, 73%). MP=173-183° C. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 8.64-8.60 (m, 1H), 8.59 (t, J=1.6 Hz, 1H), 8.50-8.46 (m, 1H), 7.98-7.94 (m, 1H), 7.86-7.83 (m, 1H), 7.78 (dd, J=7.8, 7.8 Hz, 1H), 7.02 (dd, J=7.1, 7.1 Hz, 1H), 6.18 (s, 1H), 3.29 (S, 3H). MS=289 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-7625b97224b248928c2c5172c90209fe
Source noteuspto-grants-2014_01