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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301335Generated: October 26, 2026

2,5-Difluorobenzaldehyde → 7-tert-Butyl-6-chloro-3-(2,5-difluorophenyl)-1,2,4-triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/2301335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DifluorobenzaldehydeHCID 137663—
Reactant4-(tert-Butyl)-3-chloro-6-hydrazinylpyridazineHCID 22987886—
CatalystTrichloroiron;hexahydrateHCID 16211236—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product7-tert-Butyl-6-chloro-3-(2,5-difluorophenyl)-1,2,4-triazolo[4,3-b]pyridazineHCID 1125574835.8%

Reaction Steps

To a slurry of 3-chloro-4-(1,1-dimethylethyl)-6-hydrazinylpyridazine (1.3 g, 6.5 mmol) in 0.1N hydrochloric acid (60 ml) was added 2,5-difluorobenzaldehyde (0.70 ml, 6.5 mmol) and the reaction mixture was stirred at room temperature for 30 minutes and then heated to 60° C. for 40 minutes. The reaction mixture was allowed to cool and the resultant solid was collected by filtration, dried and dissolved in ethanol (60 ml). To this solution was added iron(III) chloride hexahydrate (5.4 g, 32.5 mmol) in ethanol (15 ml) dropwise over 10 minutes at 80° C. The reaction mixture was stirred at 80° C. for 2 h, allowed to cool and the solvent removed by evaporation under vacuum. The residue was dissolved in dichloromethane (100 ml) and washed with water (3×100 ml), brine, dried (MgSO4), filtered and concentrated under vacuum to yield the title compound (0.75 g). Data for the title compound: 1H NMR (250 MHz, CDCl3) δ1.57 (9H, s), 7.22-7.29 (2H, m), 7.65-7.71 (1H, m), 8.19 (1H, s); MS (ES+) m/e 323 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500828B1
Source datasetuspto-grants-2002_12
ORD IDord-084b0bba01fc42d286291012c2f08901
Source noteuspto-grants-2002_12