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HRID 375257作成日:2026年10月26日

Acetic Acid → 3-Cyano-7,8-difluoro-1-methyl-4-oxo-1,2,3,4-tetrahydrobenzo[b][1,8]naphthyridine

https://huagongshe.com/reaction/375257

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3-ethoxycarbonyl-6,7-difluoro-2-(N-methyl-N-beta-cyanoethylamino)quinolineHCID 18994609—
反応物Water ethanolHCID 19096565—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物3-Cyano-7,8-difluoro-1-methyl-4-oxo-1,2,3,4-tetrahydrobenzo[b][1,8]naphthyridineHCID 1899459198.1%

反応条件

温度-10 °C

反応手順

A solution of 19.17 g of 3-ethoxycarbonyl-6,7-difluoro-2-[N-methyl-N-(β-cyanoethyl)amino]quinoline in 50 cm3 of tetrahydrofuran is introduced in the course of 60 minutes into a solution, cooled to -10° C., of 8.74 g of potassium tert-butylate in 200 cm 3 of tetrahydrofuran. The suspension obtained is stirred, still at -10° C., for a further 30 minutes. 4 cm3 of glacial acetic acid are then .introduced. The tetrahydrofuran is evaporated off under reduced pressure (20 kPa). The crude reaction mixture is taken up with 200 cm3 of an aqueous-alcoholic ethanol/water (70/30 vol/vol) mixture. The precipitate obtained is filtered off, washed with twice 50 cm3 of water and then dried under reduced pressure (20 kPa). 16.1 g of 3-cyano-7,8-difluoro-1-methyl-4-oxo-1,2,3,4tetrahydrobenzo[b][1,8]naphthyridine are isolated in the form of a golden-yellow solid, melting point 144° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05484921
出典データセットuspto-grants-1996_01
ORD IDord-1a1ac345f45244798de9be8861e58aad
出典メモuspto-grants-1996_01