HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633152Generated: October 30, 2026
4-[methyl(methylsulfonyl)amino]benzoic acid → HCID 58614856, compound
https://huagongshe.com/reaction/633152
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-[methyl(methylsulfonyl)amino]benzoic acid | HCID 1809372 | — |
| Reactant | 4-Chloro-3-(pyridin-2-yl)aniline | HCID 40151925 | — |
| Product | HCID 58614856 | HCID 58614856 | — |
Reaction Steps
500 mg of methyl 4-(methylamino)benzoate was cooled to 0° C. in DCM with 270 μL of Pyridine before 260 μL Methanesulfonyl Chloride was added dropwise. Reaction was allowed to warm to room temperature and stir overnight. Solvent was concentrated and the crude material was dissolved in Ethyl Acetate and extracted with 0.1N NaOH solution twice. Crude material was dried over Magnesium Sulfate, filtered and concentrated to give methyl 4-(N-methylmethylsulfonamido)benzoate. 698 mg of methyl 4-(N-methylmethylsulfonamido)benzoate was hydrolyzed via Procedure M to give 4-(N-methylmethylsulfonamido)benzoic acid. 100 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 4-(N-methylmethylsulfonamido)benzoic acid via Procedure G. The crude product was purified by reverse phase HPLC to yield pure N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(N-methylmethylsulfonamido)benzamide. MS (Q1) 416.3 (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-1cc8a1b2d42e49caa6a5e38d5be350b7 |
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| Source note | uspto-grants-2016_04 |
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