HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817823Generated: October 31, 2026
Potassium Carbonate → 5-Oxo-2-(5-phenyl-thiophen-2-yl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile
https://huagongshe.com/reaction/1817823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (5-Phenylthiophen-2-yl)boronic acid | HCID 2776315 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 2-Chloro-5-oxo-5,6,7,8-tetrahydroquinoline-3-carbonitrile | HCID 24777942 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Oxo-2-(5-phenyl-thiophen-2-yl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile | HCID 11416247 | 46% |
Reaction Steps
To a solution of 2-chloro-5-oxo-5,6,7,8-tetrahydro-quinoline-3-carbonitrile (300 mg, 1.46 mmol) and 5-phenyl-thiophen-2-yl-boronic acid (446 mg, 2.19 mmol) in dioxane (3 ml) under an argon atmosphere was added tetrakis(triphenylphosphine)palladium (85 mg, 0.073 mmol) and 2M aqueous K2CO3 (0.7 ml). The mixture was stirred at reflux till complete (TLC; hexane-EtOAc, 2:1) consumption of 2-chloro-5-oxo-5,6,7,8-tetrahydro-quinoline-3-carbonitrile. Then water was added and the mixture was extracted by dichloromethane. The extract was concentrated under reduced pressure and the residue was purified by column chromatography on silica gel (CH2Cl2-Hexane, 1:1), then heated under reflux in ethyl alcohol and filtered to give the title compound (220 mg, 46%) as a dark yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598384B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-f9bf2a320ee44ca581c1f20e596b1a9e |
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| Source note | uspto-grants-2009_10 |
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