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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

反応式

関与物質

役割名称HCID仕込み量
反応物8-Azabicyclo[3.2.1]octan-3-olHCID 68147—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-(2-azidoethyl)-1H-benzimidazole-5-carboxylic acidHCID 86630058—
溶媒DimethylformamideHCID 6228—
生成物[1-(2-azidoethyl)-1H-benzimidazol-5-yl]-(3-hydroxy-8-azabicyclo[3.2.1]oct-8-yl)methanoneHCID 8663005998%

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053431B2
出典データセットuspto-grants-2011_11
ORD IDord-5e615b6ab9244c5f843b5aa422e26add
出典メモuspto-grants-2011_11