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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3196Erstellt: 23. Oktober 2026

4-(4-Methylpiperazin-1-yl)butan-1-amine → 2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 32

https://huagongshe.com/de/reaction/3196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(4-Methylpiperazin-1-yl)butan-1-amineHCID 6484192—
Edukt6-(2,6-Dichlorophenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 10736701—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 32HCID 5327879—

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

A mixture of 0.152 g (0.43 mmol) of 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8-pyrido[2,3-d]pyrimidin-7-one of Example 37 and 0.50 g (2.90 mmol) of 1-(4-aminobutyl)-4-methylpiperazine was heated with stirring in a 170° C. oil bath. After 2 minutes, solution was complete. After 2 hours, the solution was cooled to room temperature, and the dark gum was dissolved in 25 mL of ether. The solution was washed with 4×5 mL of water. Most of the color went into the water wash. The ether solution was dried over potassium carbonate, filtered, and concentrated to ca. 2 mL volume. The crystals that separated on inducement were filtered and washed with ether; wt 0.063 g; mp 130°-132° C.;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05733914
Quelldatensatzuspto-grants-1998_03
ORD IDord-93c51878ae8a413eb4db15ce380f4843
Quellennotizuspto-grants-1998_03