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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661813Generated: October 28, 2026

Ethyl Acetate → 6-(Difluoro(6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo(4,3-b)pyridazin-3-yl)methyl)quinoline

https://huagongshe.com/reaction/1661813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazineHCID 54595607—
Reactant2,2-Difluoro-2-(quinolin-6-yl)acetohydrazideHCID 58955250—
Solvent1-ButanolHCID 263—
Product6-(Difluoro(6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo(4,3-b)pyridazin-3-yl)methyl)quinolineHCID 4691186362%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-pyridazine (step d) (4.57 g, 23.6 mmol) and difluoro-quinolin-6-yl-acetic acid hydrazide (step c) (5.60 g, 23.6 mmol) in n-butanol (125 mL) was heated to 130° C. overnight. The mixture was cooled to room temperature, followed by aqueous work up using AcOEt and a solution of K2CO3. The organic layer was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash column chromatography (first chromatography: CH2Cl2 100% and CH2Cl2/MeOH:88/12 followed by another column with toluene/iPrOH/NH4OH:85/15/2) to give the title compound (5.5 g, 62%). M.p=199.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030305B2
Source datasetuspto-grants-2011_10
ORD IDord-7db86ceab84d447193db1e541efba2ab
Source noteuspto-grants-2011_10