戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2101719作成日:2026年10月26日

1-Aminopiperidine → N-(Piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamide

https://huagongshe.com/reaction/2101719

反応式

関与物質

役割名称HCID仕込み量
反応物1-AminopiperidineHCID 16658—
反応物Ethyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylateHCID 22066075—
生成物N-(Piperidin-1-yl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamideHCID 10183243—

反応条件

温度90 °C

反応手順

A mixture of ethyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylate (50 mg, 0.125 mmol) from Step D in neat 1-aminopiperidine (1 mL) was heated at 90° C. for 72 hr. Most of the amine was evaporated under a stream of nitrogen and the residue was purified by Prep TLC (2×1 mm, silica) (40% ethyl acetate in hexanes to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07572785B2
出典データセットuspto-grants-2009_08
ORD IDord-32a9b6ea237a4719b9ecba72c5ce1b06
出典メモuspto-grants-2009_08