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HRID 2233368作成日:2026年10月26日
2-[2-(oxiran-2-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dione → 2-{4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-3-hydroxybutyl}-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/2233368
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-[2-(oxiran-2-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dione | HCID 339433 | — |
| 反応物 | 4-(3,4-Dichlorophenoxy)piperidine | HCID 3732042 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-{4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-3-hydroxybutyl}-1H-isoindole-1,3(2H)-dione | HCID 59296049 | 36.2% |
反応手順
A mixture of 4-(3,4-dichlorophenoxy)piperidine (WO 0058305, WO 0177101) (4.40 g) and 2-(2-oxiran-2-ylethyl)-1H-isoindole-1,3(2H)-dione (J. Med. Chem. 1979, 22(6), 631-9. 5.00 g) in ethanol (50 ml) was stirred at 60° C. for 12 h. The mixture was cooled down and left overnight. The formed crystals were collected by filtration, washed with cold ethanol and dried under vacuum to afford the sub-title compound as a white solid (3.0 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07709500B2 |
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| 出典データセット | uspto-grants-2010_05 |
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| ORD ID | ord-7b0a51debb4a4553a01f0c4cebb620a5 |
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| 出典メモ | uspto-grants-2010_05 |
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