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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408464Generated: October 30, 2026

1,2-Dichloroethane → cis (+/-)-1-Benzyl 3-methyl 5-(tert-butoxycarbonylamino)piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/408464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMethanolHCID 887—
Reactant2-Amino-3,4-dimethylpyridineHCID 11007884—
ReactantHCID 86656441HCID 86656441—
SolventDichloromethaneHCID 6344—
Productcis (+/-)-1-Benzyl 3-methyl 5-(tert-butoxycarbonylamino)piperidine-1,3-dicarboxylateHCID 95731685—

Reaction Steps

To a solution of cis (+/−)-1-(benzyloxycarbonyl)-5-(tert-butoxy-carbonylamino)piperidine-3-carboxylic acid (1.0 eq), methanol (20 eq.) and EDC (1.3 eq) in dichloromethane at a concentration of 0.25 M at 0° C. was added dimethyl-aminopyridine (0.1 eq). After stirring for 48 hours as the reaction was allowed to warm to rt the volatiles were removed in vacuo. Upon addition of ethyl acetate and washing with H2O (3×), 1N HCl, NaHCO3 (sat.) and brine, the solution was dried over MgSO4, filtered, concentrated and purified by column chromatography (25% ethyl acetate/hexanes) to yield cis (+/−)-1-benzyl 3-methyl 5-(tert-butoxycarbonylamino)-piperidine-1,3-dicarboxylate. LCMS (m/z): 293.1 (MH-Boc+); LC Rt=4.09 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759338B2
Source datasetuspto-grants-2014_06
ORD IDord-d09fa4df7f1746e8aeb841c0abd2696c
Source noteuspto-grants-2014_06