HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593702Generated: October 25, 2026
Potassium Phosphate, Tribasic → HCID 178469763, compound
https://huagongshe.com/reaction/593702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Ethyl 5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxylate | HCID 3816953 | — |
| Reactant | Tricyclohexylphosphonium Tetrafluoroborate | HCID 11710396 | — |
| Reactant | 1,4-Dichloro-5-phenylphthalazine | HCID 90424412 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Ammonium formate | HCID 2723923 | — |
| Product | HCID 178469763 | HCID 178469763 | 51.8% |
Reaction Steps
To a solution of 1,4-dichloro-5-phenylphthalazine (5.00 g, 18.2 mmol) in 1,4-dioxane (50 mL) and water (9 mL) was added ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (5.32 g, 27.3 mmol), and K3PO4 (7.72 g, 36.3 mmol). The contents were purged with nitrogen for 10 min. Tricyclohexylphosphonium tetrafluoroborate (0.402 g, 1.09 mmol) was added followed by Pd2(dba)3 (0.416 g, 0.454 mmol) and the reaction mixture was heated at 95° C. for 12 h. The reaction mixture was allowed to cool to ambient temperature and diluted with HCOONH4 buffer (pH˜5) solution. The reaction mixture was extracted with EtOAc (3×75 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was triturated with EtOAc to afford ethyl 5-(4-hydroxy-5-phenylphthalazin-1-yl)nicotinate (3.50 g, 44.1%) as an off-white solid which is 85% pure by LC-MS. LCMS (Condition 1): retention time 2.52 min, [M+1]=372.0. 1H NMR (400 MHz, DMSO-d6) δ 1.37 (t, J=7.2 Hz, 3 H), 4.41 (q, J=7.2 Hz, 2 H), 7.33-7.42 (m, 5 H), 7.62-7.65 (m, 2 H), 7.92 (dd, J=7.6 Hz, J=8.0 Hz, 1 H), 8.49 (t, J=2.0 Hz, 1 H), 9.07 (d, J=2.0 Hz, 1 H), 9.25 (d, J=2.0 Hz, 1 H), 12.74 (br s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242966B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b159a69123c8400baa6d818e58940d52 |
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| Source note | uspto-grants-2016_01 |
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