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HRID 612157作成日:2026年10月27日

1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2) → 4-(3-Dimethylamino-phenylamino)-5,8-dimethoxy-quinoline-3-carbonitrile

https://huagongshe.com/reaction/612157

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2)HCID 77124—
反応物1-EthoxyethanolHCID 10129898—
反応物4-Chloro-5,8-dimethoxyquinoline-3-carbonitrileHCID 22466535—
溶媒PyridineHCID 1049—
生成物4-(3-Dimethylamino-phenylamino)-5,8-dimethoxy-quinoline-3-carbonitrileHCID 2246673677.2%

反応手順

A mixture of 0.148 g of 4-chloro-5,8-dimethoxy-3-quinolinecarbonitrile, 0.146 g of N,N-dimethyl-1,3-phenylenediamine dihydrochloride, 0.2 ml of pyridine, and 5 ml of ethoxyethanol was stirred under nitrogen, at reflux temperature for 30 minutes. Then the mixture was partitioned between ethyl acetate and saturated sodium chloride solution. The organic layer was dried and concentrated in vacuo. The residue thus obtained was chromatographed on silica gel eluting with ethyl acetate. Solvent was removed from product fractions giving 0.160 g of 4-(3-dimethylamino-phenylamino)-5,8-dimethoxy-quinoline-3-carbonitrile as a solid, mp 103-105° C.; mass spectrum (EI, m/e): M 348.1588.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06002008
出典データセットuspto-grants-1999_12
ORD IDord-9a9221bcd5094dbea5d4910619fe94c9
出典メモuspto-grants-1999_12