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HRID 993406作成日:2026年10月25日

4-(5-Isopropoxythien-2-ylmethyl)-phenylamine → 2-[4-(5-Isopropoxythien-2-ylmethyl)phenyl]amino-imidazoline

https://huagongshe.com/reaction/993406

反応式

関与物質

役割名称HCID仕込み量
反応物4-(5-Isopropoxythien-2-ylmethyl)-phenylamineHCID 12094395—
反応物2-Chloroimidazoline sulfateHCID 12503398—
溶媒DichloromethaneHCID 6344—
生成物2-[4-(5-Isopropoxythien-2-ylmethyl)phenyl]amino-imidazolineHCID 1209439490%

反応条件

温度80 °C

反応手順

To a solution of 4-(5-isopropoxythien-2-ylmethyl)-phenylamine (131 mg, 0.53 mmol) in aceonitrile (8 ml) was added 2-chloro-2-imidazoline sulfate (121 mg, 0.59 mmol) at 20-25° C. under argon. The mixture was heated at 80° C. for 1.5 hours. The mixture was diluted with dichloromethane and washed with sodium hydroxide, water, dried (Na2SO4) and concentrated to dryness. Purification by preparative TLC, eluting with ethyl acetate/methyl alcohol/isopropylamine, gave 2-[4-(5-isopropoxythien-2-ylmethyl)phenyl]amino-imidazoline (150 mg, 90%) as a thick yellow oil; 1H NMR (300 Mhz, CDCl3δ 7.13 (d, J=8.4 Hz, 2H) 6.93 (d, J=8.4 Hz, 2H), 6.37 (dt, J=3.7, 1.0 Hz, 1H), 6.02 (d, J=3.7 Hz, 1H), 4.28 (quintet, J=6.2 Hz, 1H), 3.93 (bs, 2H), 3.52 (5, 4H), 3.24-3.5 (broad, 2H), 1.32 (d, J=6.2 Hz, 6H), MS m/e (%):316 (M+1, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06472536B1
出典データセットuspto-grants-2002_10
ORD IDord-22764d3580aa48f5a8f5f51a17e5d8e6
出典メモuspto-grants-2002_10