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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655949Generated: October 30, 2026

Hydrochloric Acid → (4-(2-Chlorobenzylcarbamoyl)piperidin-4-yl)methyl 4-ethylphenylcarbamate hydrochloride

https://huagongshe.com/reaction/655949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant4-Ethylphenyl isocyanateHCID 90007—
ReactantTert-butyl 4-(2-chlorobenzylcarbamoyl)-4-(hydroxymethyl)piperidine-1-carboxylateHCID 59778532—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(4-(2-Chlorobenzylcarbamoyl)piperidin-4-yl)methyl 4-ethylphenylcarbamate hydrochlorideHCID 69162882151.9%

Reaction Steps

To a solution of tert-butyl 4-(2-chlorobenzylcarbamoyl)-4-(hydroxymethyl)piperidine-1-carboxylate (1.8 g, 4.8 mmol) in THF were added DMAP (118 mg, 0.9 mmol, 0.1 equiv.) and 4-ethylphenylisocyanate (1.1 mL, 7.3 mmol, 1.5 equiv.) at r. t. The reaction mixture was stirred for 1 h. The reaction mixture was concentrated to dryness. To a solution of the above product in CH3OH was added 4M HCl in dioxane (3.6 mL, 3 equiv.), which was stirred overnight. The white solid was filtered and dried to give (4-(2-chlorobenzylcarbamoyl)piperidin-4-yl)methyl 4-ethylphenylcarbamate hydrochloride (1.7 g, 81%). LRMS (M-Boc+H+) m/z 430.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071625B2
Source datasetuspto-grants-2011_12
ORD IDord-ef3e93dd584441b6980db12e10372fda
Source noteuspto-grants-2011_12