Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349239Generated: October 25, 2026

Ethyl Acetate → 3-(4-[1,2,3]Triazol-1-yl-butyl)-6-{2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyridazine

https://huagongshe.com/reaction/349239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium t-butoxideHCID 23676156—
Reactant{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanolHCID 68934459—
Reactant3-Chloro-6-(4-[1,2,3]triazol-1-yl-butyl)-pyridazineHCID 86074068—
SolventTetrahydrofuranHCID 8028—
Product3-(4-[1,2,3]Triazol-1-yl-butyl)-6-{2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyridazineHCID 69488948—

Reaction Steps

{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanol (0.050 g, 0.17 mmol) is dissolved in anhydrous tetrahydrofuran (THF) (2 ml) followed by addition of sodium tert-butoxide (NaOtBu) (0.019 g, 0.19 mmol). After stirring for 15 min at r.t. 3-chloro-6-(4-[1,2,3]triazol-1-yl-butyl)-pyridazine (0.035 g, 0.15 mmol) is added slowly and stirred for further 4 h at 60° C. Ethyl acetate (20 ml) is added, the mixture is washed with saturated ammonium chloride (NH4Cl), dried over Na2SO4 and concentrated in vacuo. After flash column chromatography (ethyl acetate/methanol 97:3) 3-(4-[1,2,3]triazol-1-yl-butyl)-6-{2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyridazine is isolated as a colorless solid. Yield 0.049 g (69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179812B2
Source datasetuspto-grants-2007_02
ORD IDord-7fb3e8088cf4486f898445e3279fa5ab
Source noteuspto-grants-2007_02