戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 723589作成日:2026年10月27日

2-Chloroimidazoline sulfate → 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline

https://huagongshe.com/reaction/723589

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloroimidazoline sulfateHCID 12503398—
反応物4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamineHCID 21876857—
溶媒IsopropanolHCID 3776—
生成物2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazolineHCID 2187680859.2%

反応手順

A mixture of 4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine (0.64 g, 2.31 mmol) and 2-chloro-2-imidazoline sulfate (0.70 g, 3.47 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes. The reaction mixture was concentrated in vacuo. The residue was diluted with water, basified with 10% sodium hydroxide solution and extracted into dichloromethane. The organic layer was washed with water and brine, dried (Na2SO4), and concentrated in vacuo. The crude product was chromatographed on neutral aluminum oxide, eluting with 5% methanol/dichloromethane, and crystallized from ethyl acetate containing some ethanol, to give 2-[4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.47 g, 59%) as a white solid, m.p. 191–192° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141584B2
出典データセットuspto-grants-2006_11
ORD IDord-f4967b3a56184524b02094eb42413ce2
出典メモuspto-grants-2006_11