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HRID 2183708Erstellt: 26. Oktober 2026

Ethanol → 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one

https://huagongshe.com/reaction/2183708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTriethylamineHCID 8471—
Edukt1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridineHCID 21983644—
Edukt2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
Lösungsmittel1-MethoxyethanolHCID 3015637—
Produkt6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-oneHCID 13553251656,9%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine 18a (100 mg, 0.5 mmol), 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b (100 mg, 0.4 mmol), and triethylamine (140 μL, 1.0 mmol) in 10 mL methoxyethanol was heated at 100° C. under nitrogen for 12 hr. The mixture was pumped to constant weight. The resulting residue was slurried with hot ethanol and allowed to reach ambient temperature. Vacuum filtration provided 95 mg of 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one, 601, [M+H]+=418, as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06900220B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-10b30f30a6b34483809b31f83eb5d43d
Quellennotizuspto-grants-2005_05