戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 131244作成日:2026年10月23日

Cyclopropaneacetic acid → 2-Cyclopropyl-1-{4-[6-fluoro-2-phenoxymethyl-3-(4-trifluoromethoxy-benzyl)-3H-benzoimidazol-5-yl]-piperazin-1-yl}-ethanone

https://huagongshe.com/ja/reaction/131244

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclopropaneacetic acidHCID 138440—
反応物5-fluoro-2-phenoxymethyl-6-piperazin-1-yl-1-(4-trifluoromethoxy-benzyl)-1H-benzoimidazoleHCID 68467102—
溶媒DichloromethaneHCID 6344—
生成物2-Cyclopropyl-1-{4-[6-fluoro-2-phenoxymethyl-3-(4-trifluoromethoxy-benzyl)-3H-benzoimidazol-5-yl]-piperazin-1-yl}-ethanoneHCID 68463597—

反応手順

0.020 ml of cyclopropyl-acetic acid (0.2 mmol) and 40 mg of 1′1-carbonyldiimidazole (0.24 mmol) were refluxed in 4 ml dichloromethane under nitrogen for 40 minutes. 100 mg 5-Fluoro-2-phenoxymethyl-6-piperazin-1-yl-1-(4-trifluoromethoxy-benzyl)-1H-benzoimidazole (0.2 mmol) were added and the resulting mixture refluxed for additional 26 h. The reaction mixture was then diluted with dichloromethane, washed with water, saturated sodium bicarbonate and brine, dried with magnesium sulfate, filtered and concentrated in vacuo, leading to 129 mg yellow solid. This residue was purified by column chromatography (24 g silicagel, dichloromethane/methanol 24:1) leading to 77 mg light yellow solid (63%). MS (ISP) 583.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384945B2
出典データセットuspto-grants-2008_06
ORD IDord-bab3d91ddc434dcdbbdbcee6d092dc76
出典メモuspto-grants-2008_06