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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1663314생성일: 2026년 10월 24일

3,4-Diaminopyridine → HCID 178514937, 화합물

https://huagongshe.com/ko/reaction/1663314

반응식

참여 물질

역할이름HCID투입량
반응물3,4-DiaminopyridineHCID 5918—
반응물5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)pentanoic acidHCID 1714918—
반응물2-{4-(3H-imidazo[4,5-c]pyridin-2-yl)butyl}isoindole-1,3-dioneHCID 66910186—
용매WaterHCID 962—
생성물HCID 178514937HCID 178514937—

반응 조건

온도210 °C

반응 단계

4 g of pyridine-3,4-diamine and 9.5 g of 5-(1,3-dioxo-1,3-dihydroisoindol-2-yl)pentanoic acid are introduced into a 250 ml round-bottomed flask, followed by 45 g of polyphosphoric acid (PPA). The solid mixture is heated to 210° C. in an oil bath. During the reaction, the transient formation of 2-{4-(3H-imidazo[4,5-c]pyridin-2-yl)butyl}isoindole-1,3-dione is noted. After heating for 16 hours, the reaction is complete. After cooling, the reaction mixture is taken up in water. The impurities are eliminated by extraction with ethyl acetate. The aqueous phase is neutralized (pH 7) with 2N sodium hydroxide. The product is recovered after 6 successive extractions with a mixture of ethyl acetate and methanol (9/1 by volume). After purification by flash chromatography silica, elution being carried out with a mixture of dichloromethane and methanol (95/5 by volume), 1.46 g of 1-{3-H-imidazo[4,5-c]pyridin-2-yl}-3,4-dihydro-2H-pyrido[2,1-a]isoindole-6-one are obtained in the form of a white solid, the characteristics of which are as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08034939B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-5d5e8c0822f24100a10e5b80a9c04de6
출처 메모uspto-grants-2011_10