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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814864Generated: October 30, 2026

Cyclopropylamine → 1-Carbethoxy-4-cyclopropylamino-3-ethylpiperidine

https://huagongshe.com/reaction/1814864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Carbethoxy-3-ethyl-4-piperidoneHCID 22278851—
SolventMethanolHCID 887—
Product1-Carbethoxy-4-cyclopropylamino-3-ethylpiperidineHCID 22278889—

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclopropylamine (14.25 g, 250 mmol) was added to the stirred solution of 1-carbethoxy-3-ethyl-4-piperidone (10 g, 50 mmol) in methanol (100 ml) and stirring was continued for 12 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (3.9 g, 62 mmol) was added to it. Cooling was removed after 10 min. and stirring was continued for 12 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to afford crude 1-carbethoxy-4-cyclopropylamino-3-ethyl piperidine. The obtained crude 1-carbethoxy-4-cyclopropylamino-3-ethylpiperidine was suspended in 7 M NaOH solution (30 ml), stirred at 130° C. for 160 hr, cooled and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to afford 4-cyclopropylamino-3-ethyl-piperidine. Yield 5.7 g (67%), C10H20N2, m/z 169, (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878713B2
Source datasetuspto-grants-2005_04
ORD IDord-1db6d087f3a74f0ea807e9dd1147fff3
Source noteuspto-grants-2005_04