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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447776Generated: October 26, 2026

Diisopropylethylamine → 1,1-Dimethylethyl 4-[(5-cyclopropyl-3-fluoro-2-nitrophenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/447776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant5-Cyclopropyl-1,3-difluoro-2-nitrobenzeneHCID 59683254—
SolventDimethylformamideHCID 6228—
Product1,1-Dimethylethyl 4-[(5-cyclopropyl-3-fluoro-2-nitrophenyl)amino]-1-piperidinecarboxylateHCID 59683270—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 1,1-dimethylethyl 4-amino-1-piperidinecarboxylate (1 eq., 1.51 mmol, 302 mg) in dry dimethylformamide (10 ml), diisopropylethylamine (1 eq., 1.51 mmol, 0.26 ml) and 5-cyclopropyl-1,3-difluoro-2-nitrobenzene (D25, 1 eq., 1.51 mmol, 300 mg) were added at room temperature and the mixture was stirred under argon at 120° C. overnight. The crude mixture was then cooled to room temperature and poured onto water (10 ml). The aqueous solution was extracted with ethyl acetate (3×100 ml) and the organics were combined and washed with water and brine alternately (5×100 ml), dried over Na2SO4, filtered and the solvent was evaporated to afford the crude compound which was purified by chromatography (30% ethyl acetate-n-hexane 60%) to yield the title compound; 300 g, 0.79 mmol, 52%, M−−H=378.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481566B2
Source datasetuspto-grants-2013_07
ORD IDord-699d35e1c38b49b0b9e170c42d6ba4d8
Source noteuspto-grants-2013_07