関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetramethyltin | HCID 11661 | — |
| 反応物 | Lithium Chloride | HCID 433294 | — |
| 反応物 | N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester | HCID 86653275 | — |
| 触媒 | HCID 178479802 | HCID 178479802 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl ester | HCID 67155284 | 50% |
反応手順
To a solution of N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (1.1 g, 1.89 mmol) in N,N-dimethylformamide (20 mL) is added lithium chloride (0.40 g, 9.5 mmol), tetramethyl tin (0.525 mL, 3.79 mmol), and bistriphenylphosphino palladium dichloride (0.066 g, 0.095 mmol). The reaction is heated to 80° C. for 16 h. The reaction is allowed to cool to ambient temperature and filtered through Celite. The filtrate is poured over water and extracted three times with dichloromethane. The combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography (4% hexanes-ethyl acetate) to afford the title compound as a white solid (0.41 g, 50% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08841291B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-457daebb59124a8c80dea501b501c76d |
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| 出典メモ | uspto-grants-2014_09 |
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