HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633259Generated: October 30, 2026
4-Bromo-2-methylbenzonitrile → HCID 59186105, compound
https://huagongshe.com/reaction/633259
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-2-methylbenzonitrile | HCID 144267 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59186105 | HCID 59186105 | — |
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 | US09321761B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-5eedfdc960b045b38a197d4788973ff1 |
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| Source note | uspto-grants-2016_04 |
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