HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80419Generated: October 29, 2026
3,6-Dichloropyridazine → HCID 86649248, compound
https://huagongshe.com/reaction/80419
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | HCID 22314747 | HCID 22314747 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86649248 | HCID 86649248 | — |
Reaction Steps
A solution of the product of Example 2 (0.30 g, 2.0 mmol) in dry toluene (10 mL) was treated with 3,6-dichloropyridazine (0.71 g, 4.8 mmol; Aldrich), tris(dibenzylideneacetone)dipalladium(0) (Pd2(dba)3; 0.037 g, 0.04 mmol; Alfa Aesar), 1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (0.057 g, 0.12 mmol; Strem), and sodium tert-butoxide (0.45 g, 4.0 mmol; Aldrich). The mixture was purged with nitrogen and heated to 90° C. for 8 hours. After cooling to room temperature, the reaction was quenched by pouring into a 5% aqueous NaHCO3 solution. The mixture was extracted with chloroform (3×), washed with brine, dried (MgSO4), filtered and concentrated. The crude product was purified by preparative HPLC [Waters 30×100 mm XBridge Prep C18, 5 μm, 40 mL/min, 5-95% gradient of acetonitrile in buffer (0.1 M aqueous ammonium bicarbonate, adjusted to pH 10 with ammonium hydroxide)] to afford the title compound: MS (DCI/NH3) m/z 265 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846661B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-82da3ac08f8140d7b4c1f0dbabccfa47 |
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| Source note | uspto-grants-2014_09 |
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