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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2183704Erstellt: 25. Oktober 2026

Triethylamine → 6,7-dimethoxy-2-[5-(4-methyl-piperazine-1-sulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]-3H-quinazolin-4-one

https://huagongshe.com/reaction/2183704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt5-(4-Methyl-piperazine-1-sulfonyl)-1,2,3,4-tetrahydro-isoquinolineHCID 21983653—
Edukt2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt6,7-dimethoxy-2-[5-(4-methyl-piperazine-1-sulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]-3H-quinazolin-4-oneHCID 13601132837,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b, (0.77 g, 3.23 mmol), 5-(4-methyl-piperazine-1-sulfonyl)-1,2,3,4-tetrahydro-isoquinoline 11a (1.25 g, 3.41 mmol) and triethylamine (0.75 g, 1.04 mL, 7.46 mmol) in DMSO (15 mL) was heated at 80° C. with stirring for 18 h. After cooling to room temperature the reaction was diluted with water. The precipitated white product was collected by filtration, washed with water, and dried to give 0.6 g of 6,7-dimethoxy-2-[5-(4-methyl-piperazine-1-sulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]-3H-quinazolin-4-one 401, mp. 230-237° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06900220B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-1a02fd9b6cfd4f12bf4e4557b49327e7
Quellennotizuspto-grants-2005_05