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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397710Generated: October 29, 2026

Methanesulfonyl chloride → 4-Ethyl-N-hexyl-4-(3-methanesulfonylaminophenyl)piperidine

https://huagongshe.com/reaction/397710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(3-aminophenyl)-4-ethyl-N-hexylpiperidineHCID 23000925—
SolventPyridineHCID 1049—
ProductAmmoniaHCID 222—
Product4-Ethyl-N-hexyl-4-(3-methanesulfonylaminophenyl)piperidineHCID 2300096562.7%

Reaction Steps

To 4-(3-aminophenyl)-4-ethyl-N-hexylpiperidine (Preparation 64, 50.0 mg, 0.174 mmol) in anhydrous pyridine (4 ml) under nitrogen at 0° C. was added methanesulfonyl chloride (0.2 ml, 1.18 mmol). The solution was stirred at room temperature for 48 h. Ice (5 g) was added and, after 30 min, the reaction mixture was extracted with dichloromethane (10 ml). The organic extract was dried (Na2SO4), filtered and concentrated in vacuo to give the crude product which was purified by silica (5 g) column chromatography, eluting with ethyl acetate:hexane:0.880 ammonia (40:60:1), then ethyl acetate:0.880 ammonia (100:1) and then methanol:ethyl acetate:0.880 ammonia (10:89:1) to give the title compound as an oil (20 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610711B2
Source datasetuspto-grants-2003_08
ORD IDord-bc32e551ea1046af9fec9947b25d66ad
Source noteuspto-grants-2003_08