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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(5-Methanesulfonyl-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 67401250 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-Methanesulfonyl-pyridin-2-yl)-piperidin-4-yl-amine | HCID 59383087 | 74.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026255B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-dc3899b554124303b495f577a7b10bfe |
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| Source note | uspto-grants-2011_09 |
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