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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methylbenzenesulfonyl chlorideHCID 522734—
Reactant5-(Piperidin-1-yl)pyridin-2-amineHCID 11298277—
SolventPyridineHCID 1049—
ProductHCID 68842273HCID 6884227325.6%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482341B2
Source datasetuspto-grants-2009_01
ORD IDord-96ec01bdd7bb4cb897db8fde3936798f
Source noteuspto-grants-2009_01