関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Triethylamine hydrochloride | HCID 11130 | — |
| 反応物 | Sodium Azide | HCID 33557 | — |
| 反応物 | benzyl N-(2-cyanoethyl)carbamate | HCID 262127 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | Benzyl carbamate | HCID 12136 | 70% |
反応手順
A mixture of (2-cyano-ethyl)-carbamic acid benzyl ester (2.6 g, 12.7 mmol), sodium azide (2.48 g, 38 mmol) and triethylamine hydrochloride (2.62 g, 19 mmol) in NMP (96 mL) was stirred at 100° C. under Ar. After 24 h, the reaction was cooled to room temperature. Additional sodium azide (1.24 g, 19 mmol) and triethylamine hydrochloride (1.3 g, 9.5 mmol) was added to the reaction mixture and the solution was heated to 100° C. under Ar. After 18 h, the reaction was diluted with water (100 mL). 1M HCl was added dropwise until the pH was slightly acidic (˜pH 4). The solution was extracted with EtOAc (3×100 mL). The combined organic layers were washed with water (3×100 mL) and brine (100 mL), dried over MgSO4, filtered and concentrated in vacuo to yield a brown oil. Flash chromatography on silica gel (0-15% MeOH in CH2Cl2) yielded 1.1 g of crude 2-(1H-tetrazol-5-yl)-ethyl]-carbamic acid benzyl ester (˜70% pure).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08552205B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-2c136a13d3024ea99f1bab752ec2a92c |
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| 出典メモ | uspto-grants-2013_10 |
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