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HRID 1192839作成日:2026年10月25日
N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine → N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamide
https://huagongshe.com/reaction/1192839
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine | HCID 44604123 | — |
| 反応物 | Methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylate | HCID 54677706 | — |
| 溶媒 | Butyronitrile | HCID 8008 | — |
| 生成物 | N-[(6-chloropyridin-3-yl)methyl]-N-(2,2-difluoroethyl)-4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxamide | HCID 86661408 | — |
反応手順
10 g of methyl 4-hydroxy-2-oxo-2,5-dihydrofuran-3-carboxylate are initially introduced in 111 g of butyronitrile and admixed with 5 g of N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethanamine. The solution is heated at 65° C. for 3 h. The solution is then extracted with 300 ml of water and then washed with 300 ml of 5% strength hydrochloric acid solution. The organic phase is dried over magnesium sulphate and the solvent is removed in vacuo. For purification, recrystallization from isopropanol is carried out.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08680285B2 |
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| 出典データセット | uspto-grants-2014_03 |
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| ORD ID | ord-33b2f7e565e44cbd870ad14183a7eeae |
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| 出典メモ | uspto-grants-2014_03 |
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