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HRID 13238作成日:2026年10月26日

2-Pyrazinecarboxylic acid → 2-pyrazin-2-yl-5,6-bis(pyridin-3-yloxy)-1H-benzimidazole

https://huagongshe.com/reaction/13238

反応式

関与物質

役割名称HCID仕込み量
反応物2-Pyrazinecarboxylic acidHCID 1047—
反応物PyridineHCID 1049—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4,5-Bis(pyridin-3-yloxy)-benzene-1,2-diamineHCID 23145472—
溶媒Ethyl AcetateHCID 8857—
生成物2-pyrazin-2-yl-5,6-bis(pyridin-3-yloxy)-1H-benzimidazoleHCID 23145176—

反応手順

7.7 mg of pyrazine-2-carboxylic acid and 20 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide monohydrochloride were added to a pyridine (1 ml) solution of 15 mg of 4,5-bis(pyridin-3-yloxy)-benzene-1,2-diamine obtained in Example 1 (step 3), and the reaction liquid was stirred overnight at room temperature. The reaction liquid was diluted with ethyl acetate, washed with saturated sodium bicarbonate solution, water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was suspended in 1 ml of phosphorus oxychloride, and the reaction liquid was stirred overnight at 100° C. Phosphorus oxychloride was evaporated away under reduced pressure, and this was diluted with ethyl acetate, washed with saturated sodium bicarbonate solution and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the residue was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=15/1+0.1% aqueous ammonia) to obtain the entitled compound as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728025B2
出典データセットuspto-grants-2010_06
ORD IDord-8f8843c2d5024eabb85295ab8e2bd373
出典メモuspto-grants-2010_06