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HRID 1663314作成日:2026年10月26日

3,4-Diaminopyridine → HCID 178514937、化合物

https://huagongshe.com/reaction/1663314

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-DiaminopyridineHCID 5918—
反応物5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)pentanoic acidHCID 1714918—
反応物2-{4-(3H-imidazo[4,5-c]pyridin-2-yl)butyl}isoindole-1,3-dioneHCID 66910186—
溶媒WaterHCID 962—
生成物HCID 178514937HCID 178514937—

反応条件

温度210 °C

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08034939B2
出典データセットuspto-grants-2011_10
ORD IDord-5d5e8c0822f24100a10e5b80a9c04de6
出典メモuspto-grants-2011_10