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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425439Generated: October 26, 2026

Hydrogen chloride-ethyl acetate → Benzyl benzyl[cis(+/-)-3-methoxypiperidin-4-yl]carbamate

https://huagongshe.com/reaction/1425439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
Reactanttert-Butyl cis(+/-)-4-{benzyl[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylateHCID 86648850—
SolventMethanolHCID 887—
ProductBenzyl benzyl[cis(+/-)-3-methoxypiperidin-4-yl]carbamateHCID 86712358—

Reaction Steps

A 4 N hydrochloric acid/ethyl acetate solution (5 ml, 20 mmol) was added to a solution of tert-butyl cis(±)-4-{benzyl[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylate obtained in Example (259b) (about 1.44 mmol) in methanol (1 mL). The mixture was stirred for one hour and the solvent was evaporated under reduced pressure. The reaction solution was diluted with ethyl acetate, washed with aqueous sodium bicarbonate solution and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-f727394ab29e480296ca03bd394412aa
Source noteuspto-grants-2015_01