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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13238생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/13238

반응식

참여 물질

역할이름HCID투입량
반응물2-Pyrazinecarboxylic acidHCID 1047—
반응물PyridineHCID 1049—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4,5-Bis(pyridin-3-yloxy)-benzene-1,2-diamineHCID 23145472—
용매Ethyl AcetateHCID 8857—
생성물2-pyrazin-2-yl-5,6-bis(pyridin-3-yloxy)-1H-benzimidazoleHCID 23145176—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8f8843c2d5024eabb85295ab8e2bd373
출처 메모uspto-grants-2010_06