HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424282Generated: November 2, 2026
3-Aminoquinoline → Ethyl (+/-)-4-(4,4,4-trifluoro-1-(quinolin-3-ylamino)butyl)benzoate
https://huagongshe.com/reaction/1424282
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Ethyl(+/-)-4-(4,4,4-trifluoro-1-((methylsulfonyl)oxy)butyl)benzoate | HCID 86718838 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl (+/-)-4-(4,4,4-trifluoro-1-(quinolin-3-ylamino)butyl)benzoate | HCID 86718839 | — |
Reaction Steps
To a solution of ethyl(+/−)-4-(4,4,4-trifluoro-1-((methylsulfonyl)oxy)butyl)benzoate (123 mg, 0.347 mmol) in acetonitrile (1.74 mL) was added 3-amino quinoline (60.6 mg, 0.416 mmol), followed by potassium phosphate (155 mg, 0.694 mmol). The resulting mixture was heated to 60° C. for 20 hours. The reaction mixture was cooled to room temperature, diluted with water (20 mL), and extracted with ethyl acetate (3×20 mL). The combined organic layers were dried over Na2SO4 and filtered, and the filtrate was concentrated under reduced pressure. Purification by silica gel flash chromatography (ethyl acetate/heptane) gave ethyl(+/−)-4-(4,4,4-trifluoro-1-(quinolin-3-ylamino)butyl)benzoate. 1H NMR (400 MHz, CDCl3) δ 8.51 (d, J=2.5 Hz, 1H), 8.06 (d, J=8.4 Hz, 2H), 7.92 (d, J=7.8 Hz, 1H), 7.50-7.44 (m, 3H), 7.44-7.35 (m, 2H), 6.81 (d, J=2.5 Hz, 1H), 4.62-4.54 (m, 1H), 4.44-4.33 (m, 3H), 2.36-2.10 (m, 4H), 1.38 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927577B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-2b6913464ea645cca9366577a949a9ae |
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| Source note | uspto-grants-2015_01 |
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