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HRID 555294作成日:2026年10月26日
8-Azabicyclo[3.2.1]octan-3-ol → [1-(2-azidoethyl)-1H-benzimidazol-5-yl]-(3-hydroxy-8-azabicyclo[3.2.1]oct-8-yl)methanone
https://huagongshe.com/reaction/555294
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 8-Azabicyclo[3.2.1]octan-3-ol | HCID 68147 | — |
| 反応物 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 反応物 | 1-(2-azidoethyl)-1H-benzimidazole-5-carboxylic acid | HCID 86630058 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | [1-(2-azidoethyl)-1H-benzimidazol-5-yl]-(3-hydroxy-8-azabicyclo[3.2.1]oct-8-yl)methanone | HCID 86630059 | 98% |
反応手順
To a solution of 1-(2-azidoethyl)-1H-benzimidazole-5-carboxylic acid (0.82 g, 0.00357 mol) in dry DMF (8.0 mL) was added with stirring HOBt (0.578 g, 0.00428 mol), DIPEA (1.9 mL, 0.0107 mol), 8-azabicyclo[3.2.1]octan-3-ol (0.5 g, 0.00393 mol) and the mixture was cooled to 0° C. To the resulting mixture was added EDCl (0.82 g, 0.00428 mol) and stirred for 15 h at ambient temperature. The reaction mixture was then diluted with ice water (100 mL), extracted with EtOAc (3×50 mL) and the combined organic phases were washed with water (3×50 mL) and saturated brine solution (50 mL). The organic phase was dried (Na2SO4) and the solvent evaporated affording (1.1 g, 98%) of [1-(2-azidoethyl)-1H-benzimidazol-5-yl]-(3-hydroxy-8-azabicyclo[3.2.1]oct-8-yl)methanone. MS-ESI m/z 341 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08053431B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-5e615b6ab9244c5f843b5aa422e26add |
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| 出典メモ | uspto-grants-2011_11 |
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