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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511327Generated: October 26, 2026

Sodium Bicarbonate → 6-((6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoxaline

https://huagongshe.com/reaction/1511327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-Hydrazinyl-6-phenylpyridazineHCID 6409842—
ReactantTert-butyl 2-(quinoxalin-6-yl)acetateHCID 67504321—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product6-((6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoxalineHCID 24964088—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of tert-butyl 2-(quinoxalin-6-yl)acetate (0.15 g, 0.6 mmol), 1-(6-phenylpyridazin-3-yl)hydrazine (0.1 g, 0.7 mmol) and p-toluenesulfonic acid monohydrate (0.1 g, 0.6 mmol) in 3 mL of dioxane was heated with microwave at 150° C. for 1 hour in a microwave tube. The mixture was diluted with 70 mL of EtOAc and 40 mL of satd. NaHCO3 solution. The organic phase was separated and was washed with 40 mL of brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (EtOAc to 15% MeOH/EtOAc) to give light yellow solid as desired product 6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoxaline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212041B2
Source datasetuspto-grants-2012_07
ORD IDord-667e46b195db4058916adf29de778b4e
Source noteuspto-grants-2012_07