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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179946Generated: October 26, 2026

Triethylamine → HCID 69519303, compound

https://huagongshe.com/reaction/1179946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 86589184HCID 86589184—
Reactant2(1H)-Pyridinone, 5-[[5-(trifluoromethyl)-2-pyridinyl]oxy]-HCID 178516274—
SolventAcetonitrileHCID 6342—
ProductHCID 69519303HCID 6951930365%

Reaction Steps

A solution of 5-(5-trifluoromethyl-pyridin-2-yloxy)-pyridin-2-ol (180 mg, 0.70 mmol), 3-[4-(tert-butyl-dimethyl-silanyloxy)-piperidine-1-carbonyl]-1-methyl-3H-imidazol-1-ium iodide (317 mg, 0.70 mmol) and triethylamine (98 μL) in acetonitrile (10 mL) was stirred at room temperature overnight. The solvent was evaporated in vacuo. The residue was redissolved in some dichloromethane, filtered over a short pad of silicagel and washed with ethyl acetate:heptane 50:50. The solvent was evaporated in vacuo and the residue was dissolved in 3.2N HCl in ether (10 mL). After stirring for 1 hour at room temperature the solvent was evaporated in vacuo and the residue was dissolved in dichloromethane. Triethylamine (0.5 mL) was added and the solution was extracted with water. The organic layer was dried over sodium sulphate, filtered and evaporated in vacuo to yield the title compound (174 mg, 65% yield) as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279470B2
Source datasetuspto-grants-2007_10
ORD IDord-a02107e333e94f2ca29f62a229380e0e
Source noteuspto-grants-2007_10