関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-Methoxy-alpha-toluenethiol | HCID 80407 | — |
| 反応物 | Ethyl acetate hexane | HCID 21226206 | — |
| 反応物 | 2-bromopentanoyl-(L)-homophenylalanine methyl ester | HCID 22950831 | — |
| 触媒 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester | HCID 22950828 | — |
反応手順
Combine 2-bromopentanoyl-(L)-homophenylalanine methyl ester (3.6 g, 10 mmol), 4-methyoxybenzylmercaptan (3.48 mL, 25 mmol), and tetrabutylammonium iodide (about 50 mg) in dimethylformamide (10 mL). Degas by repeatedly applying vacuum and filling the vessel with nitrogen. Add cesium carbonate (4.10 g, 12.5 mmol). After 15 hours, partition the reaction mixture between water and methyl t-butyl ether, saturate the aqueous layer with sodium chloride. Extract the aqueous layer with brine, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 4/1 hexane/ethyl acetate and then 2.5/1 hexane/ethyl acetate to give the title compound: Rf=0.44 (silica gel, 2.5/1 hexane/ethyl acetate).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06352976B1 |
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| 出典データセット | uspto-grants-2002_03 |
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| ORD ID | ord-d1385ca9dc824c218ae0cd8094c64e04 |
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| 出典メモ | uspto-grants-2002_03 |
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