HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388130Generated: November 1, 2026
Potassium Carbonate → HCID 24985023, compound
https://huagongshe.com/reaction/388130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Quinolin-5-ylboronic acid | HCID 5153389 | — |
| Reactant | HCID 66699904 | HCID 66699904 | — |
| Reactant | HCID 86626408 | HCID 86626408 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 24985023 | HCID 24985023 | 77% |
Reaction Steps
((1R)-1-Phenylethyl)(5-nitro-2-(5-quinolyl)(4-pyridyl))amine. ((1R)-1-Phenylethyl)(2-bromo-5-nitro(4-pyridyl))amine (5.6g, 1.75 mmol)and 5-quinolineboronic acid (393 mg, 2.27 mmole) were dissolved in DMF (25 ml). Nitrogen gas was bubbled into solution for 2 min. Potassium carbonate (970 mg, 7.00 mmol) in water (5 mL) was then added followed by tetrakis(triphenylphosphine)palladium (0) (0.175 mmol). The solution was then heated to 85° C. under nitrogen for 1 h. The solution was condensed under reduced pressure and the crude product was diluted with ethyl acetate and filtered through a plug of silica-gel. The resultant filtrate was condensed under reduced pressure to afford the title compound (502 mg, 77%). MS (ESI) m/z 371 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372976B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-08f976e773ff475986a21ba2379acd57 |
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| Source note | uspto-grants-2013_02 |
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