関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | tert-butyl N-(1-cyanocyclopropyl)carbamate | HCID 20825555 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | tert-butyl N-(1-carbamimidoylcyclopropyl)carbamate | HCID 58430989 | 109% |
反応手順
(1-Cyano-cyclopropyl)-carbamic acid tert-butyl ester (2.44 g, 13.40 mmol) was dissolved in dry EtOH (33 mL). Sodium ethoxide (21 wt % in EtOH solution, 10.70 mL, 22.80 mmol)) was added and the reaction was stirred for 1 h at room temperature under an atmosphere of dry argon. To the light yellow solution was added solid NH4Cl (2.94 g, 55 mmol) followed by 7 M NH3 in MeOH (8.08 mL, 56.60 mmol). The reaction was capped and allowed to stir for 16 h. The turbid suspension was filtered using MeOH to rinse. The filtrate was concentrated in vacuo and the solid residue was re-suspended in dry EtOH. The solids were filtered off, rinsing with EtOH. The filtrate was concentrated to give 2.91 g of (1-Carbamimidoyl-cyclopropyl)-carbamic acid tert-butyl ester as a light yellow solid. m/z 200.48 [M+1]+
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-373987b60a034396b7874d2d38168718 |
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| 出典メモ | uspto-grants-2013_10 |
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