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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929996Generated: October 27, 2026

Methanol → 4-(2,5-Difluorophenyl)-5-(3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)oxazole

https://huagongshe.com/reaction/1929996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Difluoro-2-(isocyano(tosyl)methyl)benzeneHCID 22170180—
Reactant3-Isopropyl-[1,2,4]triazolo[4,3-b]pyridazine-6-carbaldehydeHCID 57929899—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-(2,5-Difluorophenyl)-5-(3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)oxazoleHCID 5792989671.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazine-6-carbaldehyde (0.150 g, 0.789 mmol, Preparation #2) in 1,4-dioxane (3 mL) was added 1,4-difluoro-2-(isocyano(tosyl)methyl)benzene (0.202 g, 0.657 mmol, Preparation #4), K2CO3 (0.218 g, 1.58 mmol) and MeOH (3.00 mL). The reaction mixture was heated to about 80° C. for about 3 h. The reaction mixture was diluted with water (50 mL) and extracted with DCM (50 mL). The organic layer was dried with MgSO4, filtered and concentrated in vacuo. The crude material was purified by silica gel chromatography using heptane/EtOAc (gradient; 1:1 to 0:1) to give the title compound (0.161 g, 71% yield). LC/MS (Table 1, Method a) Rt=2.20 min; MS m/z: 342.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188083B2
Source datasetuspto-grants-2012_05
ORD IDord-eca2dc0467944336a96f81b616d61fed
Source noteuspto-grants-2012_05