HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456552Generated: October 29, 2026
Quinoline → 1-[4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-ethanone
https://huagongshe.com/reaction/456552
Participants
| Role | Name | HCID | Charge |
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| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 3-(1-Acetyl-piperidin-4-yl)-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid | HCID 23112425 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-ethanone | HCID 23112505 | 74% |
Reaction Steps
A mixture of 3-(1-acetyl-piperidin-4-yl)-7-trifluoromethyl-benzo[b]thiophene-2-carboxylic acid (4.13 g, 11.1 mmol), Cu powder (0.706 g, 11.1 mmol), and quinoline (20 mL) was heated to 200° C. under nitrogen. After 10 min, no gas evolution was observed and the reaction cooled at room temperature. The mixture was diluted with ethyl acetate (100 mL), filtered through a Celite bed and the filtrate washed with 1 N HCl (2×100 mL), 5% aqueous potassium carbonate (100 mL), water (100 mL), and brine (100 mL) successively. The organics were dried over magnesium sulfate, filtered, and concentrated to give an amber oil. The oil was chromatographed on silica, eluting with 10% methanol/ethyl acetate to afford 2.69 g (74%) of the desired product as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186724B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-a0d4d6f6ef9d4edda8e4d141db3f36f3 |
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| Source note | uspto-grants-2007_03 |
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