HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925432Generated: October 31, 2026
Potassium Carbonate → HCID 57824527, compound
https://huagongshe.com/reaction/1925432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Aminophenylboronic acid | HCID 2734615 | — |
| Reactant | HCID 43583892 | HCID 43583892 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57824527 | HCID 57824527 | 56% |
Reaction Steps
To a solution containing 3-chloro-6-(4-trifluoromethoxyphenyl)-pyridazine (157 mg, 0.57 mmol), 4-aminophenylboronic acid (118 mg, 0.86 mmol) and 2 M K2CO3 (0.57 mL, 1.14 mmol) dissolved in 3.5 mL of dry 1,4-dioxane was added dichlorobis(triphenylphosphine)palladium(II) (4 mg, 0.006 mmol). The mixture was irradiated using a CEM Discover microwave at 190° C. for 30 min. The mixture was diluted with 100 mL of ether and washed with brine (30 mL). The organic phase was then dried over MgSO4, filtered and concentrated. The residue was purified via radial chromatography using a 97:3 CHCl3/CH3OH solution as the eluent (Rf=0.26) to afford the title compound (105 mg, 56%). 1H NMR (400 MHz, CDCl3) δ 8.18 (d, J=8.6 Hz, 2H), 8.01 (d, J=8.6 Hz, 2H), 7.30-7.45 (m, 4H), 6.82 (d, J=8.6 Hz, 2H), 3.96 (bs, 2H); EIMS 331 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178658B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-3d5dcd0e6d3449f7b706f174747a7f3f |
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| Source note | uspto-grants-2012_05 |
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