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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889772Generated: October 30, 2026

4-(Methanesulfonyl)phenylboronic acid → HCID 49838518, compound

https://huagongshe.com/reaction/1889772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
ReactantHCID 67481418HCID 67481418—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
ProductHCID 49838518HCID 49838518—

Reaction Steps

[8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-(3-methoxy-phenyl)-amine was prepared from (8-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-(3-methoxy-phenyl)-amine (200.0 mg, 0.6266 mmol) and (4-methylsulfonylphenyl)boronic acid (150.0 mg, 0.7499 mmol) with Pd(dppf)Cl2 (50.0 mg) as the catalyst in a manner analogous to Step 2c and was isolated as a yellow solid (0.097 g, 39%). MP=204-206° C. 1H NMR (400 MHz, CDCl3, δ, ppm): 8.50 (d, J=6.1 Hz, 1H), 8.24 (d, J=7.8 Hz, 2H), 8.08 (d, J=7.7 Hz, 2H), 7.66 (d, J=7.4 Hz, 1H), 7.37 (s, 1H), 7.28-7.22 (m, 1H), 7.08-7.00 (m, 2H), 6.92 (s, 1H), 6.58 (d, J=7.6 Hz, 1H), 3.86 (s, 3H), 3.10 (s, 3H). MS=395 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501936B2
Source datasetuspto-grants-2013_08
ORD IDord-07d02c373008403897995f69da63464b
Source noteuspto-grants-2013_08