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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Ethyl 2-aminocyclohex-1-ene-1-carboxylate | HCID 312929 | — |
| Reactant | 5-(4-Quinoline-2-ylpiperazin-1-yl)hexanoic acid | HCID 23155918 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 2-[5-(4-quinolin-2-ylpiperazin-1-yl)hexanoylamino]cyclohex-1-enecarboxylate | HCID 23155828 | 38.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799775B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-6a77593a7b5c477a9a546085ff9cac5b |
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| Source note | uspto-grants-2010_09 |
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