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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-(5-Isopropoxythien-2-ylmethyl)-phenylamine | HCID 12094395 | — |
| 反応物 | 2-Chloroimidazoline sulfate | HCID 12503398 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-[4-(5-Isopropoxythien-2-ylmethyl)phenyl]amino-imidazoline | HCID 12094394 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06472536B1 |
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| 出典データセット | uspto-grants-2002_10 |
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| ORD ID | ord-22764d3580aa48f5a8f5f51a17e5d8e6 |
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| 出典メモ | uspto-grants-2002_10 |
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