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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714788Generated: November 1, 2026

Phosphorus trichloride → Ethyl 2-[5-(4-quinolin-2-ylpiperazin-1-yl)hexanoylamino]cyclohex-1-enecarboxylate

https://huagongshe.com/reaction/1714788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
ReactantEthyl 2-aminocyclohex-1-ene-1-carboxylateHCID 312929—
Reactant5-(4-Quinoline-2-ylpiperazin-1-yl)hexanoic acidHCID 23155918—
SolventPyridineHCID 1049—
ProductEthyl 2-[5-(4-quinolin-2-ylpiperazin-1-yl)hexanoylamino]cyclohex-1-enecarboxylateHCID 2315582838.1%

Reaction Steps

To a solution of 170 mg of ethyl 2-aminocyclohex-1-enecarboxylate as synthesized in Step 7-1-B in 5 ml of pyridine, 70 mg of phosphorus trichloride was added under cooling with ice, followed by 15 minutes' stirring. Raising the temperature to room temperature, 327 mg of 5-(4-quinoline-2-ylpiperazin-1-yl)hexanoic acid as synthesized in above Step 7-14-C was added to the solution and stirred for 3 hours. Distilling the pyridine off under reduced pressure, the residue was extracted with ethyl acetate and washed with water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified on silica gel column chromatography (ethyl acetate) to provide 182 mg (38%) of ethyl 2-[5-(4-quinolin-2-ylpiperazin-1-yl)hexanoylamino]cyclohex-1-enecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-6a77593a7b5c477a9a546085ff9cac5b
Source noteuspto-grants-2010_09