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HRID 19653Erstellt: 24. Oktober 2026

1,4-Dioxane → 5,6,7,8-Tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/de/reaction/19653

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DioxaneHCID 31275—
EduktDimethylacetamideHCID 31374—
Edukt2-Chloro-5-methyl-pyridineHCID 581393—
Edukt5,6,7,8-Tetrahydropyrido[4,3-d]pyrimidin-4(3H)-oneHCID 135627628—
LösungsmittelChloroform isopropyl alcoholHCID 21906603—
Produkt5,6,7,8-Tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidin-4(3H)-oneHCID 13597895748,5%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

Into a 20 ml microwave tube was combined 5,6,7,8-Tetrahydro-3H-pyrido[4,3-d]pyrimidin-4-one (0.280 g, 0.00183 mol), 2-chloro-5-methylpyridine (0.47 g, 0.0037 mol), 1,4-dioxane (2.5 mL, 0.032 mol) N,N-diisopropylethylamine (0.64 mL, 0.0037 mol) and N,N-dimethylacetamide (0.5 mL, 0.005 mol). The mixture was heated via microwave at 150° C. for 4 hours. The mixture was reduced in vacuo and taken up in chloroform:IPA (3:1) (50 ml). The organic was washed with sodium bicarbonate and brine (1×50 ml), dried over sodium sulfate, and reduced in vacuo. The mixture was purified by flash chromatography on silica gel using a methylene chloride:methanol (0-10%) gradient. The combined pure fractions were reduced in vacuo to yield a bright yellow solid (0.215 g, 47.9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745451B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-f5fb789182c64475b71a7962bb9ce2e6
Quellennotizuspto-grants-2010_06