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HRID 392177作成日:2026年10月27日

Ammonia → 3,4-Dimethoxy-6-nitrobenzamide

https://huagongshe.com/reaction/392177

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Thionyl ChlorideHCID 24386—
反応物4,5-Dimethoxy-2-nitrobenzoic acidHCID 78690—
生成物3,4-Dimethoxy-6-nitrobenzamideHCID 2736193—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800649B1
出典データセットuspto-grants-2004_10
ORD IDord-b1a56db9ed184ae2822cd44cd51538db
出典メモuspto-grants-2004_10