HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092044Generated: November 1, 2026
Potassium Carbonate → HCID 59574401, compound
https://huagongshe.com/reaction/2092044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | HCID 11484080 | HCID 11484080 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59574401 | HCID 59574401 | 19.2% |
Reaction Steps
2-[1-(3,6-Dichloropyridazin-4-yl)ethyl]isoindoline-1,3-dione (161 mg, 0.5 mmol), trimethylboroxine (0.209 mL, 1.5 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) dichloromethane complex (35.1 mg, 0.05 mmol) and potassium carbonate (82.9 mg, 0.6 mmol) were mixed with water (0.2 mL) and 1,4-dioxane (0.9 mL) and stirred at 110° C. for 8 hours. After completion of the reaction, the reaction solution was cooled to room temperature, and the solvent was removed by vacuum distillation. The resulting residue was mixed with 4 M hydrogen chloride/1,4-dioxane (10 mL) and stirred at room temperature for 16 hours. After completion of the reaction, the reaction solution was mixed with water and extracted with chloroform, and the extract was dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The resulting residue was purified by preparative thin-layer chromatography (hexane/ethyl acetate=1/1) to give the desired product (29 mg, 19% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440666B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-00a030d08e3e4bc781aad948fb15e3a4 |
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| Source note | uspto-grants-2013_05 |
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