HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80418Generated: October 24, 2026
3-Chloro-6-phenylpyridazine → 4-(6-Phenylpyridazin-3-yl)-1,4-diazatricyclo[4.3.1.13,8]undecane
https://huagongshe.com/en/reaction/80418
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-6-phenylpyridazine | HCID 88515 | — |
| Reactant | 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride | HCID 2734913 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(6-Phenylpyridazin-3-yl)-1,4-diazatricyclo[4.3.1.13,8]undecane | HCID 49870776 | — |
Reaction Steps
A solution of the product of Example 2 (0.10 g, 0.66 mmol) in dry toluene (10 mL) was treated with 3-chloro-6-phenylpyridazine (0.20 g, 1.0 mmol; Aldrich), tris(dibenzylideneacetone)dipalladium(0) (Pd2(dba)3; 0.01 g, 0.013 mmol; Alfa Aesar), 1,3-bis(2,6-di-iso-propylphenyl)imidazolium chloride (0.017 g, 0.04 mmol; Strem), and sodium tert-butoxide (0.148 g, 1.32 mmol). 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 flash chromatography on silica gel, eluting with 2-10% methanol (containing 1% ammonium hydroxide)-chloroform to afford the title compound: MS (DCI/NH3) m/z 307 (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-ac62a457a9a341128a0cf870cc90b89f |
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| Source note | uspto-grants-2014_09 |
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