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HRID 551915作成日:2026年10月27日
Ethanesulfonyl chloride → Methyl (4-{[{4-[(4-butylphenyl)ethynyl]benzyl}(ethylsulfonyl)-amino]methyl}phenoxy)acetate
https://huagongshe.com/reaction/551915
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanesulfonyl chloride | HCID 11667 | — |
| 反応物 | Methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)methyl]phenoxy}acetate | HCID 57554567 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Methyl (4-{[{4-[(4-butylphenyl)ethynyl]benzyl}(ethylsulfonyl)-amino]methyl}phenoxy)acetate | HCID 11555583 | 15.3% |
反応手順
To a cold solution (0° C.) of methyl {4-[({4-[(4-butylphenyl)ethynyl]benzyl}amino)-methyl]phenoxy}acetate (38 mg, 0.086 mmol) in anhydrous pyridine (2 mL) was added ethanesulfonyl chloride (Fluka, 40 ∞l, 0.43 mmol) and the reaction mixture was stirred at 0° C. for 4 hrs and at rt for an additional 15 hours. The reaction mixture was diluted with an aqueous solution of HCl (1N) and extracted with DCM (3×). The combined organic layers were dried over MgSO4 and the solvent was removed under reduced pressure. Purification by flash chromatography on silicagel (cHex/EtOAc) gave 7 mg (15%) of the title compound as a colorless oil. LC/MS, M+(ESI): 534.3 (purity: 94.5%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07947851B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-5f15bf8530b94124adec123fba881f2f |
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| 出典メモ | uspto-grants-2011_05 |
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