Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266306Generated: November 1, 2026

Phosphorus oxychloride → 3-Chloro-6-(2-chlorophenyl)-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/2266306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-(2-chlorophenyl)-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-oneHCID 59641677—
Product3-Chloro-6-(2-chlorophenyl)-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 57979757100%

Reaction Conditions

Temperature130 °C

Reaction Steps

A suspension of 6-(2-chlorophenyl)-7-(4-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (1.0 g, 2.8 mmol) in phosphorus oxychloride (10 mL) was stirred at 130° C. for 6 h. Analysis by HPLC/MS indicated the starting material had been consumed. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The obtained residue was diluted with CH2Cl2, the resulting solution washed with saturated aqueous NaHCO3, saturated aqueous NaCl, dried (Na2SO4) and concentrated under reduced pressure to afford 1.1 g (100%) of the title compound as an off-white solid. HPLC/MS (method A): retention time=3.52 min, (M+H)+=375.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858639B2
Source datasetuspto-grants-2010_12
ORD IDord-35ff24ec67924203af536398b150664c
Source noteuspto-grants-2010_12