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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427048Generated: November 3, 2026

Hydrochloric Acid → 6-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)pyridine-3-carboxylic acid

https://huagongshe.com/reaction/1427048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 6-(1-(tert-butoxycarbonyl)piperidin-4-yl)nicotinateHCID 86730350—
SolventEthanolHCID 702—
Product6-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)pyridine-3-carboxylic acidHCID 8673034952%

Reaction Steps

A 2 M sodium hydroxide solution (20 mL) was added to a solution of methyl 6-(1-(tert-butoxycarbonyl)piperidin-4-yl)nicotinate described in Production Example 28-2 (1.07 g, 3.32 mmol) in ethanol (5 mL), and the mixture was stirred for 1 hour. 2 M hydrochloric acid was added to the reaction liquid at 0° C. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with a saturated saline solution and then dried over anhydrous sodium sulfate. The drying agent was separated by filtration and then the filtrate was concentrated under vacuum to obtain the title compound (534 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933099B2
Source datasetuspto-grants-2015_01
ORD IDord-4f2dfd6fb92c4eea90ae5c4f177f9485
Source noteuspto-grants-2015_01