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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [3-(4-Cyclohexylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-carbamic acid tert-butyl ester | HCID 86706523 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(3-Amino-benzyl)-piperidine-4-carboxylic acid cyclohexylamide | HCID 86706524 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09428456B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-0d48e3b40a5c450fad1747784f1ac016 |
|---|
| Source note | uspto-grants-2016_08 |
|---|