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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090956Generated: October 25, 2026

Methanol → 1-[2-(6-Methyl-2-pyridyl)ethyl]-4-(4-methylsulfonylaminophenylsulfonyl)piperidine

https://huagongshe.com/reaction/1090956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Ethenyl-6-methylpyridineHCID 70735—
ReactantSodium AcetateHCID 517045—
Reactant4-(4-Methylsulfonylaminophenylsulfonyl)piperidine hydrochlorideHCID 18539239—
SolventWaterHCID 962—
Product1-[2-(6-Methyl-2-pyridyl)ethyl]-4-(4-methylsulfonylaminophenylsulfonyl)piperidineHCID 1502772264%

Reaction Steps

0.60 g (1.86 mmol) of 4-(4-methylsulfonylaminophenylsulfonyl)piperidine hydrochloride obtained in Example 5, 0.44 g (3.72 mmol) of 6-methyl-2-vinylpyridine and 0.31 g of sodium acetate were suspended in 10 ml of a mixture of methanol with water (1:1) and the suspension was refluxed for 2 h. The reaction liquid was filtered and the filtrate was concentrated to give a residue. After extraction with dichloromethane followed by washing with water, the organic layer was concentrated to precipitate white crystals. The crystals were collected by filtration and recrystallized from ethyl acetate to give 0.52 g (yield: 64%) of the intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082850
Source datasetuspto-grants-1992_01
ORD IDord-bc76334c947d411dad1abc35c67b41bb
Source noteuspto-grants-1992_01