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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472309Generated: November 1, 2026

4-(Isopropylsulphonyl)benzeneboronic acid → 8-[4-(Propane-2-sulfonyl)-phenyl]-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine

https://huagongshe.com/reaction/472309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Isopropylsulphonyl)benzeneboronic acidHCID 44119327—
Reactant8-Bromo-(1,2,4)triazolo(1,5-a)pyridin-2-amineHCID 46864069—
Product8-[4-(Propane-2-sulfonyl)-phenyl]-[1,2,4]triazolo[1,5-a]pyridin-2-ylamineHCID 67481399—

Reaction Steps

8-[4-(Propane-2-sulfonyl)-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 (500.0 mg, 2.347 mmol) and 4-isopropylsulfonylbenzeneboronic acid (650.0 mg, 2.850 mmol) in a manner analogous to Step 2c. The reaction product was isolated as an off-white solid (0.317 g, 42%). MP=175-177° C. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 8.64 (d, J=6.6 Hz, 1H), 8.39 (d, J=7.4 Hz, 2H), 7.96 (d, J=7.5 Hz, 2H), 7.85 (d, J=7.4 Hz, 1H), 7.06-7.00 (m, 1H), 6.21 (br s, 2H), 3.54-3.42 (m, 1H), 1.19 (d, J=6.5 Hz, 6H). MS=317 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-c52a87c48d644642b6dc7a0b124a3e90
Source noteuspto-grants-2014_01