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HRID 427421作成日:2026年10月24日

Ammonia → 3,4-Dimethoxy-6-nitrobenzamide

https://huagongshe.com/ja/reaction/427421

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 (1) was treated with thionyl chloride and then reacted with ammonia to give 4,5-dimethoxy-2-nitrobenzamide (2) as described by F. Nomoto et al. Chem. Pharm. Bull. 1990, 38, 1591-1595. The nitro group in compound (2) 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 (3) which was cyclized by refluxing with formic acid to give 6,7-dimethoxyquinazoline-4(3H)-one (4). Compound (4) was refluxed with phosphorus oxytrichloride to provide compound (5), which is a useful intermediate for preparing compounds of formula I wherein X is NH. Reaction of compound (5) with the requiste aniline provided the following compounds of formula I:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313129B1
出典データセットuspto-grants-2001_11
ORD IDord-c59fe4d23757427894acf97329f02fe0
出典メモuspto-grants-2001_11