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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349234Generated: October 31, 2026

Ethyl Acetate → 5-(4-[1,2,3]Triazol-1-yl-butyl)-2-{2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyrimidine

https://huagongshe.com/reaction/349234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium t-butoxideHCID 23676156—
Reactant{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanolHCID 68934459—
Reactant2-Chloro-5-(4-[1,2,3]triazol-1-yl-butyl)-pyrimidineHCID 86074066—
SolventTetrahydrofuranHCID 8028—
Product5-(4-[1,2,3]Triazol-1-yl-butyl)-2-{2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyrimidineHCID 69135788—

Reaction Steps

{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanol (0.097 g, 0.34 mmol) is dissolved in anhydrous tetrahydrofuran (THF) (4 ml) followed by addition of sodium tert-butoxide (NaOtBu) (0.040 g, 0.41 mmol). After stirring for 15 min at r.t. 2-chloro-5-(4-[1,2,3]triazol-1-yl-butyl)-pyrimidine (0.090 g, 0.38 mmol) is added slowly and stirred for further 1.5 h at r.t. Ethyl acetate (20 ml) is added; the mixture is washed with saturated ammonium chloride (NH4Cl), dried over MgSO4 and concentrated in vacuo. After flash column chromatography (ethyl acetate) 5-(4-[1,2,3]triazol-1-yl-butyl)-2-{2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyrimidine is obtained as a colorless solid. Yield 0.104 g (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179812B2
Source datasetuspto-grants-2007_02
ORD IDord-54d7261538974307915f91f2c6e820cc
Source noteuspto-grants-2007_02