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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486692Generated: October 31, 2026

Hydrochloric Acid → 1-(3-Amino-benzyl)-piperidine-4-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/1486692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant[3-(4-Cyclohexylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-carbamic acid tert-butyl esterHCID 86706523—
Solvent1,4-DioxaneHCID 31275—
Product1-(3-Amino-benzyl)-piperidine-4-carboxylic acid cyclohexylamideHCID 86706524—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of [3-(4-cyclohexylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-carbamic acid tert-butyl ester (4.6 g, 11.1 mmol) in 1,4-dioxane (110 mL) is cooled down to 0° C. and treated with a 4N HCl solution in 1,4-dioxane (24.9 mL, 99.6 mmol). The reaction mixture is heated to 60° C. for 1 h. The reaction mixture is cooled down to RT and treated with aqueous 2N sodium hydroxide. After evaporation of 1,4-dioxane under reduced pressure the reaction mixture is extracted twice with DCM (110 mL). The combined organic phases are dried over MgSO4 and evaporated to yield the title compound as a yellowish powder: LC-MS A: tR=0.50 min; [M+H]+=316.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428456B2
Source datasetuspto-grants-2016_08
ORD IDord-0d48e3b40a5c450fad1747784f1ac016
Source noteuspto-grants-2016_08