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HRID 1436520作成日:2026年10月26日
1,2-Diaminocyclohexane, trans- → 4-[2-(3-Methyl-butyl)-phenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1436520
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| 反応物 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 反応物 | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| 反応物 | 1-Iodo-2-(3-methyl-butyl)-benzene | HCID 54130445 | — |
| 触媒 | Copper iodide | HCID 83717 | — |
| 生成物 | 4-[2-(3-Methyl-butyl)-phenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester | HCID 69017615 | 29.2% |
反応手順
Charge in a pressure tube copper iodide (16 mg, 0.08 mmol), potassium phosphate (717 g, 3.4 mmol), trans-1,2-diaminocyclohexane (0.020 ml, 0.17 mmol), 1-Iodo-2-(3-methyl-butyl)-benzene (462 mg, 1.7 mmol) and 3-oxo-piperazine-1-carboxylic acid tert-butyl ester (405 g, 2.02 mmol). Purge with nitrogen and add 2 ml of dry 1,4-dioxane. Cap the tube and stir at 120° C. overnight. Filter through celite eluting with EtOAc and concentrate. Purify in a silica gel cartridge (10 g) eluting with hexane followed by EtOAc/hexane 1:1 to give the title compound as a yellow solid (172 mg, 29%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07618978B2 |
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| 出典データセット | uspto-grants-2009_11 |
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| ORD ID | ord-41629d7925de4b56abd75f6a17d7ae1d |
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| 出典メモ | uspto-grants-2009_11 |
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