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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 392177Erstellt: 26. Oktober 2026

Ammonia → 3,4-Dimethoxy-6-nitrobenzamide

https://huagongshe.com/reaction/392177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktThionyl ChlorideHCID 24386—
Edukt4,5-Dimethoxy-2-nitrobenzoic acidHCID 78690—
Produkt3,4-Dimethoxy-6-nitrobenzamideHCID 2736193—

Reaktionsschritte

4,5-Dimethoxy-2-nitrobenzoic acid (3) was treated with thionyl chloride and then reacted with ammonia to give 4,5-dimethoxy-2-nitrobenzamide (4) as described by F. Nomoto et al. Chem. Pharm. Bull. 1990, 38, 1591-1595. The nitro group in compound (4) was reduced with sodium borohydride in the presence of copper sulfate (see C. L. Thomas Catalytic Processes and Proven Catalysts Academic Press, New York (1970)) to give 4,5-dimethoxy-2-aminobenzamide (5) which was cyclized by refluxing with formic acid to give 6,7-dimethoxyquinazoline-4(3H)-one (6). Compound (6) was refluxed with phosphorus oxytrichloride to provide the common synthetic precursor (7).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06800649B1
Quelldatensatzuspto-grants-2004_10
ORD IDord-b1a56db9ed184ae2822cd44cd51538db
Quellennotizuspto-grants-2004_10