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HRID 1831322作成日:2026年10月27日

Triethylamine → HCID 69519303、化合物

https://huagongshe.com/reaction/1831322

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物HCID 86589184HCID 86589184—
反応物2(1H)-Pyridinone, 5-[[5-(trifluoromethyl)-2-pyridinyl]oxy]-HCID 178516274—
溶媒AcetonitrileHCID 6342—
生成物HCID 69519303HCID 6951930365%

反応手順

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, chloromethane, 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07067517B2
出典データセットuspto-grants-2006_06
ORD IDord-bf52efe4eb644f84b2fec4380809f47d
出典メモuspto-grants-2006_06