HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751292Generated: October 30, 2026
Potassium Fluoride → HCID 10070332, compound
https://huagongshe.com/reaction/751292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Reactant | HCID 58611972 | HCID 58611972 | — |
| Reactant | (2-pyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-3-boronic acid | HCID 59710031 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10070332 | HCID 10070332 | 5.5% |
Reaction Steps
Add N-(6-bromo-[1,8]naphthyridin-2-yl)-2-dimethylamino-acetamide (148 mg, 0.48 mmol), 2-(pyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-3-boronic acid (Preparation 5; 100 mg, 0.44 mmol), potassium fluoride (84 mg, 1.45 mmol), and THF (1.5 mL) to a flask under nitrogen. Purge the system with nitrogen for 10 min and add tris(dibenzylideneacetone)dipalladium(0) (40 mg, 0.044 mmol) and tri-tert-butylphosphonium tetrafluoroborate (Strem; 25 mg, 0.088 mmol). Purge the system with nitrogen for 2 min then stir for 16 h at room temperature. Add additional tris(dibenzylideneacetone)dipalladium(0) (50 mg, 0.054 mmol) and tri-tert-butylphosphonium tetrafluoroborate (40 mg, 0.138 mmol) and heat the reaction to 65° C. for 9 h. Filter the reaction through Celite®, rinse with chloroform/methanol, and concentrate in vacuo. Purify by flash column chromatography followed by reverse-phase preparative HPLC. Collect the pure fractions from the HPLC, concentrate in vacuo, take up the residue in methanol, and treat with MP-carbonate beads. Filter, concentrate in vacuo, and triturate with hexanes to provide the title compound (10 mg, 5%) as a tan solid. MS ESI+ m/e 414 (M+1). 1H NMR (CDCl3) δ 10.21 (m, 1H), 8.93 (m, 1H), 8.48 (m, 2H), 8.09 (m, 2H), 7.68 (m, 2H), 7.20 (m, 1H), 4.27 (m, 2H), 3.17 (m, 4H), 2.72 (m, 2H), 2.41 (s, 6H). HPLC: 95.1%, Rt=11.21 min. TLC (SiO2): Rf0.3 (1:1 [80:18:2 chloroform/methanol/concentrated aqueous ammonium hydroxide]/dichloromethane)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405299B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-70059814244b459bb87692fcb395239d |
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| Source note | uspto-grants-2008_07 |
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