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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472349Generated: October 29, 2026

3-Methylsulfonylaminophenylboronic acid → HCID 67481412, compound

https://huagongshe.com/reaction/472349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylsulfonylaminophenylboronic acidHCID 2773535—
Reactant5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
ProductHCID 67481412HCID 6748141218%

Reaction Steps

N-[3-(2-Amino-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-phenyl]-methanesulfonamide was prepared from 5-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (1.80 g, 8.45 mmol) and 3-methylsulfonylaminophenyl boronic acid (2.0 g, 9.30 mmol), in a manner analogous to Step 73c. The residue was purified on an 80 g Isco silica gel column using a gradient of 0-7% methanol in dichloromethane as an eluent. N-[3-(2-Amino-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-phenyl]-methanesulfonamide (461 mg, 18%) was isolated as a beige powder. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 9.94 (s, 1H), 7.72 (s, 1H), 7.64 (d, J=7.5 Hz, 1H), 7.51 (m, 2H), 7.38 (d, J=8.6 Hz, 1H), 7.32 (d, J=7.5 Hz, 1H), 6.97 (d, J=7.5 Hz, 1H), 6.03 (br s, 2H), 3.08 (s, 3H). MS=304 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-500932c7bf3b4d4a937b729f9114289d
Source noteuspto-grants-2014_01