戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2383953作成日:2026年10月27日

Methanol → 1-[3-Fluoro-4-(2,2,2-trifluoroacetyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/2383953

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物1-[3-Fluoro-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 59636227—
触媒Manganese dioxideHCID 14801—
溶媒DichloromethaneHCID 6344—
生成物1-[3-Fluoro-4-(2,2,2-trifluoroacetyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963619474.53%

反応条件

温度50 °C

反応手順

MnO2 (536 mg, 6.165 mmol) was added to 1-[3-fluoro-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-197a: 325 mg, 0.880 mmol) in DCM (20 mL) under nitrogen atmosphere. The resulting suspension was stirred at 50° C. overnight. The reaction was monitored by TLC (5% MeOH in DCM). The reaction mixture was cooled to room temperature and filtered through celite pad. The filtrate was washed with CHCl3, dried over Na2SO4 and concentrated. The concentrate was washed with hexane and dried to afford 240 mg of the product (74.53% yield).

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-ee4cf1edb9684516b09950ee39a97b67
出典メモuspto-grants-2012_09