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HRID 239862作成日:2026年10月27日
Sodium methanesulfonate → (s)-2-[(s)-1-(4-Bromo-phenyl)-2,2,2-trifluoro-ethylamino]-4-methyl-pentanoic acid [(s)-1-cyano-2-(4-methanesulfonyl-phenyl)-ethyl]-amide
https://huagongshe.com/reaction/239862
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium methanesulfonate | HCID 638112 | — |
| 反応物 | N2-[(1S)-1-(4-bromophenyl)-2,2,2-trifluoroethyl]-N-[(1S)-1-cyano-2-(4-iodophenyl)ethyl]-L-leucinamide | HCID 68779205 | — |
| 触媒 | Copper iodide | HCID 83717 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | (s)-2-[(s)-1-(4-Bromo-phenyl)-2,2,2-trifluoro-ethylamino]-4-methyl-pentanoic acid [(s)-1-cyano-2-(4-methanesulfonyl-phenyl)-ethyl]-amide | HCID 42633519 | — |
反応手順
To N2-[(1S)-1-(4-bromophenyl)-2,2,2-trifluoroethyl]-N-[(1S)-1-cyano-2-(4-iodophenyl)ethyl]-L-leucinamide (1 eq) in DMSO (0.3 M) were added methane sulfonic acid sodium salt (2 eq) and copper iodide (3 eq) and the mixture was stirred at 100° C. for 2 h. The reaction mixture was cooled and diluted with EtOAc. The organic layer was washed with brine and water, dried over Na2SO4, filtered and concentrated. The crude compound was purified by automated SiO2 flash chromatography system using solvent gradient of 40% EtOAc/Hex to 100% EtOAc/Hex.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08642799B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-53f846116d2044d497afa95b5c656f0a |
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| 出典メモ | uspto-grants-2014_02 |
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