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HRID 2383789作成日:2026年10月27日

Potassium Carbonate → 1-Naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/2383789

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1,2-Diaminocyclohexane, trans-HCID 43806—
反応物3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
反応物1-Naphthalen-2-yl-imidazolidin-2-oneHCID 59636167—
触媒Copper iodideHCID 83717—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物1-Naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963621652%

反応条件

温度110 °C

反応手順

Copper iodide (12.6 mg, 0.066 mmol), trans-1,2-diamino cyclohexane (22.79 mg, 0.199 mmol) and potassium carbonate (183.5 mg, 1.32 mmol) were added to 1,4-dioxane (5 mL) and 3-bromo-5-trifluoromethyl-pyridine (150 mg, 0.66 mmol) previously degassed with argon (10 minutes). The reaction was purged with argon for a further 10 minutes, followed by the addition of 1-naphthalen-2-yl-imidazolidin-2-one (I-79b: 140 mg, 0.66 mmol) and the resulting mixture was heated to reflux at 110° C. for 15 hours. The reaction was monitored by TLC (50% ethyl acetate in hexane). The reaction mixture was filtered through celite and the bed was washed with chloroform. The organic layer was dried over Na2O4 and concentrated. Purification by column chromatography (using silica gel of mesh size of 60-120, 30% EtOAc in hexane as eluant) afforded 120 mg (52% yield) of 1-naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08263635B2
出典データセットuspto-grants-2012_09
ORD IDord-686da2ace8444d299cbf0901bc9566d1
出典メモuspto-grants-2012_09