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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075720Generated: October 31, 2026

Glycol monoethyl ether → 1,1,1-Trifluoro-2-[2-(1-phenyl-[1,2,4]triazolo[4,3-a]quinolin-7-ylsulfanyl)-thiazol-5-yl]-butan-2-ol

https://huagongshe.com/reaction/2075720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycol monoethyl etherHCID 8076—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Iodo-1-phenyl-[1,2,4]triazolo[4,3-a]quinolineHCID 58257758—
ReactantHCID 178472193HCID 178472193—
CatalystCopper iodideHCID 83717—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product1,1,1-Trifluoro-2-[2-(1-phenyl-[1,2,4]triazolo[4,3-a]quinolin-7-ylsulfanyl)-thiazol-5-yl]-butan-2-olHCID 67090867—

Reaction Conditions

Temperature90 °C

Reaction Steps

7-Iodo-1-phenyl-[1,2,4]triazolo[4,3-a]quinoline (10c, 140 mg, 0.38 mmol), copper iodide (14 mg, 0.08 mmol), and potassium carbonate (105 mg, 0.76 mmol) were suspended in iPrOH (1 mL). 10b (92 mg, 0.38 mmol) in iPrOH (1 mL) was added, followed by ethyl glycol (0.04 mL, 0.76 mmol), and the reaction was heated to 90° C. overnight. The reaction was diluted with EtOAc and water, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel chromatography (5% MeOH in CH2Cl2), and the isolated product was precipitated from CH2Cl2 to give the desired product, 10d.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919621B2
Source datasetuspto-grants-2011_04
ORD IDord-b99293a7aa1346f4922e1fa8c3d16d6e
Source noteuspto-grants-2011_04