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HRID 280006Erstellt: 25. Oktober 2026

8-Quinolinamine, 7-methyl- → 5-(8-Amino-7-methyl-5-quinolylmethyl)-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/280006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt8-Quinolinamine, 7-methyl-HCID 231556—
Edukt5-[(dimethylamino)methyl]-1H-pyrimidine-2,4-dione;hydrochlorideHCID 12267435—
LösungsmittelEthylene GlycolHCID 174—
Produkt5-(8-Amino-7-methyl-5-quinolylmethyl)-2,4(1H,3H)-pyrimidinedioneHCID 2012981978%

Reaktionsschritte

A mixture of 8.36 g (0.0406 mole) of 5-[(dimethylamino)methyl]uracil hydrochloride (B. Roth, J. Z. Strelitz, and B. S. Rauckman, J. Med. Chem. 23, 379 (1980) and 6.43 g (0.0406 mole) of 8-amino-7-methylquinoline (R. Long and K. Schofield, J. Chem. Soc. 1953, 2350) in 60 ml of ethylene glycol under nitrogen was heated at 135° for 4 hours. The mixture was cooled and the precipitated solid was collected, washed with ethanol and ether and dried. This crude product was purified by suspension in 550 ml of boiling ethanol and collection of the insoluble product. Yield, 8.90 g of the title compound (78%) m.p. 302°-305° (dec.). Anal. Calcd for C21H20N4 : C, 76.80; H, 6.14; N, 17.06. Found: C, 76.82; H, 6.17; N, 17.04.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04587342
Quelldatensatzuspto-grants-1986_05
ORD IDord-24a39a5f29af4dbd86deee576c73f081
Quellennotizuspto-grants-1986_05