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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913148Generated: October 26, 2026

Hydrochloric Acid → (5-Methanesulfonyl-pyridin-2-yl)-piperidin-4-yl-amine

https://huagongshe.com/reaction/913148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant4-(5-Methanesulfonyl-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 67401250—
SolventEthanolHCID 702—
Product(5-Methanesulfonyl-pyridin-2-yl)-piperidin-4-yl-amineHCID 5938308774.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 4-(5-methanesulfonyl-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (1.00 g, 2.8 mmol, 1.0 equiv) in ethanol (18 mL) was added 4 M HCl in dioxane (3.52 mL, 14.1 mmol, 5.0 equiv) drop by drop and the reaction mixture stirred at 50° C. for 2 h. It was then cooled down to rt, poured into ice water and the pH adjusted to 9-10 by addition of a sat. solution of potassium carbonate. The solution was extracted six times with a mixture of dichloromethane/isopropanol (4:1). The combined organic layers were concentrated by evaporation under reduced pressure and the crude product was purified by crystallization from heptane to give 0.53 g (74%) of the title compound as colorless solid. MS (ISP): 256.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026255B2
Source datasetuspto-grants-2011_09
ORD IDord-dc3899b554124303b495f577a7b10bfe
Source noteuspto-grants-2011_09