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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456062Generated: October 31, 2026

3,6-Dichloropyridazine → 6-((6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)difluoromethyl)quinoline

https://huagongshe.com/reaction/456062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-DichloropyridazineHCID 67331—
Reactant2,2-Difluoro-2-(quinolin-6-yl)acetohydrazideHCID 58955250—
Solvent1-ButanolHCID 263—
Product6-((6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)difluoromethyl)quinolineHCID 5769103353.5%

Reaction Conditions

Temperature130 °C

Reaction Steps

3,6-dichloropyridazine (160 mg, 1.07 mmol) and difluoro-quinolin-6-yl-acetic acid hydrazide (254 mg, 1.07 mmol) were added in n-BuOH (20 mL). The reaction mixture was heated to 130° C. for 12 hours. The solvent was removed by vacuo. The crude was extracted by the solution of K2CO3 and EtOAc. The organic layer was collected and concentrated to give a solid, which was purified by silica gel column to give 6-[(6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)-difluoro-methyl]-quinoline as a black solid (190 mg, 53%). 1H-NMR (DMSO) δ ppm 7.62 (m, 2H); 7.90 (m, 1H); 8.22 (m, 1H); 8.35 (m, 1H); 8.65 (m, 2H); 9.02 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497368B2
Source datasetuspto-grants-2013_07
ORD IDord-ce19703066fa4f49b919a5014d2c945b
Source noteuspto-grants-2013_07