HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394554Generated: October 30, 2026
Pyridine → N-3-Quinolinylbenzenesulfonamide
https://huagongshe.com/reaction/394554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-3-Quinolinylbenzenesulfonamide | HCID 16654646 | — |
Reaction Steps
To a solution of 3-aminoquinoline (7.2 g, 50 mmol) in acetonitrile (150 mL) was added pyridine (25 mL) and the resulting mixture was cooled to 0° C. A solution of benzenesulfonyl chloride (7 mL, 55 mmol) in acetonitrile (20 mL) was added dropwise over 30 minutes. The mixture was allowed to warm to rt and stirred for 18 hours. The mixture was diluted with ethyl acetate (100 mL) and washed successively with 1N HCl, brine and saturated CuSO4, dried (MgSO4), and concentrated in vacuo to afford an oil. Purification by flash silica gel column chromatography eluting with 30% ethyl acetate in hexanes afforded compound C (13. g g, 95%) as a white solid. MS; (M+H)+=285
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602883B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-be7dfc7e9e8c4e32b0ec01ae27d2bc73 |
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| Source note | uspto-grants-2003_08 |
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