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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716576Generated: November 2, 2026

4-Nitrophenyl 2,2-diethoxypropanoate → HCID 68510828, compound

https://huagongshe.com/reaction/1716576

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl 2,2-diethoxypropanoateHCID 13807233—
Reactant1,1-Dimethylethyl 4-[(2-amino-4-methylphenyl)amino]-1-piperidinecarboxylateHCID 58852288—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 68510828HCID 6851082862%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(2-Amino-4-methyl-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (400 mg, 1.31 mmol), p-nitrophenyl 2,2-diethoxyproprionate (1.00 g, 3.50 mmol), and DMAP (1.00 g, 8.2 mmol) were combined in acetonitrile (3 mL) and heated in an oil bath at 80° C. for 2 h. The mixture was cooled, diluted with diethyl ether (100 mL), washed once each with saturated aqueous NH4Cl and water, three times with 5% aqueous sodium hydroxide solution, once with brine and dried over anhydrous MgSO4 and concentrated under reduced pressure. The residue was adsorbed on a silica gel pad, and the pad was eluted with 25% ethyl acetate in hexanes to give 4-[2-(2,2-diethoxy-propionylamino)-4-methyl-phenylamino]-piperidine-1-carboxylic acid tert-butyl ester (550 mg, 0.81 mmol, 62%) of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803816B2
Source datasetuspto-grants-2010_09
ORD IDord-44aa94696a0c49c28e957422a891ee39
Source noteuspto-grants-2010_09