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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-phenylpyridazineHCID 88515—
Reactant1,3-Bis(2,6-diisopropylphenyl)imidazolium chlorideHCID 2734913—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product4-(6-Phenylpyridazin-3-yl)-1,4-diazatricyclo[4.3.1.13,8]undecaneHCID 49870776—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846661B2
Source datasetuspto-grants-2014_09
ORD IDord-ac62a457a9a341128a0cf870cc90b89f
Source noteuspto-grants-2014_09