HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472089Generated: October 30, 2026
Phenylhydrazine → HCID 59860240, compound
https://huagongshe.com/reaction/472089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 66782052 | HCID 66782052 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59860240 | HCID 59860240 | 6% |
Reaction Steps
A solution of phenylhydrazine (0.093 ml, 0.95 mmol) in anhydrous THF (4.0 ml) was treated with a 1M solution of potassium tert-butoxide in THF (1.89 ml, 1.89 mmol). The resulting solution was added to a solution of ethyl 3-[4-(4-pyridinyl)-6-quinolinyl]-2-propynoate (0.268 g, 0.95 mmol) in THF (10 ml). The resulting brown solution was stirred at room temperature for 1 hour then at 65° C. for 1 hour. The resulting orange slurry was cooled to room temperature then concentrated under reduced pressure. The resulting residue was taken into saturated aqueous NaHCO3 then extracted into methylene chloride and the extracts were dried over sodium sulfate then evaporated under reduced pressure. The resulting oil was purified by HPLC (acetonitrile/water, 5-80% gradient). The product was concentrated to a residue then recrystallized from ethanol to give the title compound (0.020 g, 6%) as a white solid. MS (ES)+ m/e 365 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633187B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-dd9df16ef5d446b3af1c7696d33b7b6a |
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| Source note | uspto-grants-2014_01 |
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