関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Aminoacetonitrile hydrochloride | HCID 11491918 | — |
| 反応物 | 2-(Methoxycarbonyl)cyclopentane-1-carboxylic acid | HCID 13239030 | — |
| 反応物 | Tripyrrolidinophosphonium hexafluorophosphate | HCID 22226026 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Methyl trans-2-{[(cyanomethyl)amino]carbonyl}cyclopentanecarboxylate | HCID 86596126 | — |
反応手順
Cyclopentane-1,2-dicarboxylic acid monomethyl ester (2.21 g, 12.8 mmol), 2-aminoacetonitrile hydrochloride (1.48 g, 16.0 mmol) and benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyBOP) (7.34 g, 14.1 mmol) were dissolved in dimethylformamide (26 mL) and the reaction mixture was cooled to 0° C. Triethylamine (4.9 mL, 35 mmol) was added and the reaction mixture was stirred at ambient temperature for 3 h. The reaction mixture was partitioned between water (150 mL) and ethyl acetate (100 mL). The product was extracted into ethyl acetate, washed with saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate and concentrated. The residue was chromatographed on silica gel with 3:2 ethyl acetate:hexanes eluent to give methyl trans-2-{[(cyanomethyl)amino]carbonyl}cyclopentanecarboxylate as a colorless solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07371747B2 |
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| 出典データセット | uspto-grants-2008_05 |
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| ORD ID | ord-00527ddaf1df475ca700b359b698bed5 |
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| 出典メモ | uspto-grants-2008_05 |
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