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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421554Generated: October 27, 2026

Methanesulfonic Acid → {4-[(2-Pyridin-3-ylpiperidin-1-yl)sulfonyl]phenyl}amine

https://huagongshe.com/reaction/421554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}phenyl)acetamideHCID 659759—
SolventMethanolHCID 887—
Product{4-[(2-Pyridin-3-ylpiperidin-1-yl)sulfonyl]phenyl}amineHCID 277092278.7%

Reaction Steps

A 1.81 ml portion of methanesulfonic acid was added to a methanol solution (10 ml) of 1.0 g N-(4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}phenyl)acetamide and stirred overnight at room temperature. The reaction liquid was poured into ice water and neutralized with sodium bicarbonate, and then layer separation operation was carried out by adding ethyl acetate. The organic layer was washed with saturated sodium chloride aqueous solution, dried with anhydrous sodium sulfate and then concentrated under a reduced pressure to obtain 695 mg of 4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}aniline as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101580B2
Source datasetuspto-grants-2012_01
ORD IDord-4b59a8b4d78b455c86b6d0f266d83bd8
Source noteuspto-grants-2012_01