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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1663314Erstellt: 25. Oktober 2026

3,4-Diaminopyridine → HCID 178514937, Verbindung

https://huagongshe.com/reaction/1663314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-DiaminopyridineHCID 5918—
Edukt5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)pentanoic acidHCID 1714918—
Edukt2-{4-(3H-imidazo[4,5-c]pyridin-2-yl)butyl}isoindole-1,3-dioneHCID 66910186—
LösungsmittelWaterHCID 962—
ProduktHCID 178514937HCID 178514937—

Reaktionsbedingungen

Temperatur210 °C

Reaktionsschritte

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:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08034939B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-5d5e8c0822f24100a10e5b80a9c04de6
Quellennotizuspto-grants-2011_10