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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633260Generated: October 31, 2026

2-Methyl-4-(methylsulfonyl)benzoic acid → HCID 58614763, compound

https://huagongshe.com/reaction/633260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-(methylsulfonyl)benzoic acidHCID 14254473—
Reactant4-Chloro-3-(pyridin-2-yl)anilineHCID 40151925—
ProductHCID 58614763HCID 58614763—

Reaction Steps

A solution of 500 mg of 4-bromo-2-methylbenzonitrile and 268 mg of sodium thiomethoxide in 3 mL of DMF was stirred for 1 h. The reaction mixture was diluted with ethyl acetate, washed with H2O, dried (MgSO4) and evaporated to afford 2-methyl-4-(methylthio)benzonitrile. 400 mg of 2-methyl-4-(methylthio)benzonitrile was reacted via Procedure T to give 2-methyl-4-(methylthio)benzoic acid. 430 mg of 2-methyl-4-(methylthio)benzoic acid was reacted via Procedure R to yield 2-methyl-4-(methylsulfonyl)benzoic acid. 60 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 2-methyl-4-(methylsulfonyl)benzoic acid via Procedure G. The product was purified on reverse phase HPLC to yield N-(4-chloro-3-(pyridin-2-yl)phenyl)-2-methyl-4-(methylsulfonyl)benzamide. MS (Q1) 401.0 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321761B2
Source datasetuspto-grants-2016_04
ORD IDord-addb064e2eb84f30953bbe6e67b215f4
Source noteuspto-grants-2016_04