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HRID 2210190Erstellt: 24. Oktober 2026

Water → 1,3-bis[4-(2-pyridylthio)butyl]quinazoline-2,4(1H,3H)-dione

https://huagongshe.com/de/reaction/2210190

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktQuinazolinedioneHCID 64048—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt2-(4-Chlorobutylthio)pyridineHCID 19079186—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,3-bis[4-(2-pyridylthio)butyl]quinazoline-2,4(1H,3H)-dioneHCID 190792329%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 1.62 g (10 mmol) of benzoylene urea and 2.02 g (10 mmol) of 2-(4-chlorobutylthio)pyridine in 50 ml of dimethylformamide, 1.65 ml (11 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added, and the mixture was stirred at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried and the solvent was distilled off. The residue was purified by column chromatography (eluent: hexane/ethyl acetate=2:1 to 1:2). First, 221 mg of the desired product was obtained (4.6% yield, yellow oil), and then, 292 mg of 3-[4-(2-pyridylthio)butyl]quinazoline-2,4(1H,3H)-dione was obtained (8.9% yield, white crystals).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05457106
Quelldatensatzuspto-grants-1995_10
ORD IDord-0808ed055632497ca21e2b2e445c50a0
Quellennotizuspto-grants-1995_10