関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 2-Amino-2'-fluoro-5-nitrobenzophenone | HCID 67657 | — |
| 反応物 | N-(Benzyloxycarbonyl)-DL-alanine | HCID 95657 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamate | HCID 20562333 | — |
反応手順
50 g of carbobenzoxy-DL-alanine are dissolved in 400 ml of absolute tetrahydrofuran, treated dropwise while cooling with ice with 30 g of thionyl chloride and stirred for 40 minutes, a suspension of 50 g of 2-amino-5-nitro-2'-fluorobenzophenone in 200 ml of absolute tetrahydrofuran then being rapidly added dropwise. Subsequently, the mixture is stirred at room temperature for 18 hours, the solution is concentrated and the residue is treated with ice and 10% sodium bicarbonate solution. The mixture is extracted with methylene chloride, the organic solution is dried with sodium sulphate, filtered and concentrated. The residue is crystallised from ethanol and yields rac-benzyl-{1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]ethyl}carbamate which is further processed directly as the crude product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04296031 |
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| 出典データセット | uspto-grants-1981_10 |
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| ORD ID | ord-d7a69e9e3dc244e2a5f268bf7949bb71 |
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| 出典メモ | uspto-grants-1981_10 |
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