HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454913Generated: October 29, 2026
3-Chloro-2-methylbenzenesulfonyl chloride → HCID 68842273, compound
https://huagongshe.com/reaction/1454913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-2-methylbenzenesulfonyl chloride | HCID 522734 | — |
| Reactant | 5-(Piperidin-1-yl)pyridin-2-amine | HCID 11298277 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68842273 | HCID 68842273 | 25.6% |
Reaction Steps
3,4,5,6-Tetrahydro-2H-[1,3′]bipyridinyl-6′-ylamine (0.19 g) and 3-chloro-2-methylbenzenesulfonyl chloride (0.24 g) were dissolved in pyridine (4 mL) and heated at 50° C. over night. The mixture was concentrated in vacuo, taken up in ethyl acetate and extracted with 1M Cu(II)SO4 solution. The organic layer was washed once again with Cu(II)SO4 solution, dried over Na2SO4 and evaporated in vacuo. The product was purified by flash chromatography on silica gel (gradient of ethyl acetate in heptane) to give 3-chloro-2-methyl-N-(3,4,5,6-tetrahydro-2H-[1,3′]bipyridinyl-6′-yl)-benzenesulfonamide (0.1 g) as a light brown foam. MS (ESI−): 364.0 ([M−H]−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482341B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-96ec01bdd7bb4cb897db8fde3936798f |
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| Source note | uspto-grants-2009_01 |
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