HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364885Generated: November 2, 2026
2-Methyl-4-(methylsulfonyl)benzoic acid → HCID 58614763, compound
https://huagongshe.com/reaction/1364885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-4-(methylsulfonyl)benzoic acid | HCID 14254473 | — |
| Reactant | 4-Chloro-3-(pyridin-2-yl)aniline | HCID 40151925 | — |
| Product | HCID 58614763 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888364B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-7cbecfedd2f142beab70c1e5332eb2d6 |
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| Source note | uspto-grants-2011_02 |
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