HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743029Generated: October 30, 2026
Hydrochloric Acid → 3-Iodo-N-(3-methyl-2-pyridinyl)benzenesulfonamide
https://huagongshe.com/reaction/743029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Amino-3-methylpyridine | HCID 15347 | — |
| Reactant | m-Iodobenzenesulphonyl chloride | HCID 39766 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 3-Iodo-N-(3-methyl-2-pyridinyl)benzenesulfonamide | HCID 19423394 | — |
Reaction Steps
32.4 g 3-methyl-2-pyridinamine (32.4 g, 0.3 mol) was dissolved in isobutylmethylketone (200 ml) and 3-iodo-benzenesulfonyl chloride (30.2 g, 0.1 mol) was added with stirring. The solution was kept at 40° C. for 8 h and then added to dilute hydrochloric acid. The precipitate was filtered off and the organic phase was separated and evaporated. The residue was combined with the first solid material and recrystallized from ethanol. The crystals were dissolved in 1M sodium hydroxide (about 200? ml) and extracted with isobutylmethylketone (3×100 ml). The aqueous phase was partially evaporated to remove isobutylmethylketone residues. Ethanol (100? ml) was added and the solution acidified with acetic acid. The precipitate was filtered off, washed with water and dried. Yield 23 g, 61%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05556855 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-a33715cf014c4ed6a3ec12f3a1e0e152 |
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| Source note | uspto-grants-1996_09 |
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