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HRID 1358843作成日:2026年10月25日
2-Chloroimidazoline sulfate → 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline
https://huagongshe.com/reaction/1358843
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Chloroimidazoline sulfate | HCID 12503398 | — |
| 反応物 | 4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine | HCID 21876857 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline | HCID 21876808 | 59.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06596876B2 |
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| 出典データセット | uspto-grants-2003_07 |
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| ORD ID | ord-64666150977c4c6288f6bf1d7f856889 |
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| 出典メモ | uspto-grants-2003_07 |
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