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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1978914Erstellt: 27. Oktober 2026

N-acetylanthranilic acid → 9-methoxy-3-(2-methyl-4-oxo-4H-quinazolin-3-yl)-1-phenyl-6,7-dihydro-3H-[1,4]diazepino [6,7,1-hi] indol-4-one

https://huagongshe.com/reaction/1978914

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-acetylanthranilic acidHCID 6971—
EduktPhosphorus trichlorideHCID 24387—
EduktSodium BicarbonateHCID 516892—
EduktPhosphorusHCID 5462309—
Edukt3-amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-oneHCID 69957132—
LösungsmittelDichloromethaneHCID 6344—
Produkt9-methoxy-3-(2-methyl-4-oxo-4H-quinazolin-3-yl)-1-phenyl-6,7-dihydro-3H-[1,4]diazepino [6,7,1-hi] indol-4-oneHCID 6995608617,3%

Reaktionsschritte

0.834 g (4.65 mmol) of acetylanthranilic acid and 1.3 g (4.23 mmol) of 3-amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one are dissolved in 13 ml of CH2Cl2, the mixture is stirred at room temperature and 0.7 g (5 mmol) of phosphorus trichloride is added. The mixture is stirred for 20 h and 0.35 g of phosphorus trichlonrde is added, followed by a fuirther 0.35 g 8 h later. The mixture is cooled, 50 ml of saturated NaHCO3 solution and 100 ml of CH2Cl2 are added and the organic phase is separated out after settling has taken place and washed with water. This solution is dried, evaporated and purified by chromatography in the mixture DM1. 0.33 g of yellow powder is obtained. M.p.=277° C.—Yld 17%.—TLC (DM3): Rf=0.47.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06239130B1
Quelldatensatzuspto-grants-2001_05
ORD IDord-f377b519db484db3a2f9106d17541b22
Quellennotizuspto-grants-2001_05