HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473941Generated: October 30, 2026
4-Toluenesulfonyl chloride → N-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamide
https://huagongshe.com/reaction/1473941
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-Amino-5-fluoropyridine | HCID 2737701 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-fluoropyridin-2-yl)-4-methylbenzenesulfonamide | HCID 57607460 | 100.7% |
Reaction Steps
2-amino-5-fluoropyridine (25 g, 0.22 mol) in pyridine (100 mL) was treated portion wise with p-toluenesulfonyl chloride (47.5 g, 0.25 mol) and heated at 80° C. for 2 hours. The cooled material was concentrated to remove the majority of pyridine. The resulting viscous solution was diluted with 200 ml of ethyl acetate then 200 ml of water. The resulting suspension was stirred for about an hour to break up the solids then filtered. The filter cake was washed with water then cold ethyl acetate, dried to afford 59 g of a light brown solid. Rf 0.43, 50% ethyl acetate/hexanes; MS m/z 266 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018208B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-b909c26ca76d47ed948027815c5fb180 |
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| Source note | uspto-grants-2015_04 |
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