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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064124Generated: October 25, 2026

Water → 1,1-Dimethylethyl 4-[(5-chloro-4-methyl-2-nitrophenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/2064124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,5-Dichloro-2-methyl-4-nitrobenzeneHCID 251679—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventDimethylformamideHCID 6228—
Product1,1-Dimethylethyl 4-[(5-chloro-4-methyl-2-nitrophenyl)amino]-1-piperidinecarboxylateHCID 59850138—

Reaction Conditions

Temperature100 °C

Reaction Steps

1,5-Dichloro-2-methyl-4-nitrobenzene (2.42 mmol, 500 mg) was dissolved in dry dimethylformamide (5 ml) and diisopropylethylamine (1 eq., 2.42 mmol, 0.413 ml), 1,1-dimethylethyl 4-amino-1-piperidinecarboxylate (1 eq., 2.42 mmol, 484 mg) were added at room temperature and the mixture was stirred at 100° C. overnight. The crude mixture was then cooled to room temperature and water was added; the aqueous solution was extracted with ethyl acetate (3×); organics were alternatively washed with brine and water. The organics were combined, dried over Na2SO4, filtered and the solvent was evaporated to afford the crude compound that was purified by chromatography (ethyl acetate/hexane) to yield the title compound, 98 mg, 11%, bright orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288412B2
Source datasetuspto-grants-2012_10
ORD IDord-299f2183c10d4f508b68f534b983dc8b
Source noteuspto-grants-2012_10