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HRID 989384作成日:2026年10月25日

Sodium Hydroxide → 4-(2,4-Dichloro-5-methoxyphenylamino)-7-methoxy-8-(2-[1,2,3]triazol-2-yl ethoxy)benzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/989384

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物4-(2,4-Dichloro-5-methoxyanilino)-7-methoxy-8-(chloroethoxy)benzo[g]quinoline-3-carbonitrileHCID 11569639—
反応物HCID 178418936HCID 178418936—
溶媒DimethylformamideHCID 6228—
生成物4-(2,4-Dichloro-5-methoxyphenylamino)-7-methoxy-8-(2-[1,2,3]triazol-2-yl ethoxy)benzo[g]quinoline-3-carbonitrileHCID 1016557521.4%

反応条件

温度80 °C

反応手順

A mixture of 0.31 g (0.62 mmol) of 8-(2-chloroethoxy)-4-(2,4-dichloro-5-methoxyphenylamino)-7-methoxybenzo[g]quinoline-3-carbonitrile, 0.36 mL (6.1 mmol) of 1H-1,2,3-triazole and 0.11 g (2.8 mmol) of sodium hydroxide powder in 5 mL of N,N-dimethyl formamide is heated at 80° C. for 4.5 hours, then cooled and poured on to ice. The solid is collected by filtration, washed with water and dried. The two isomers are separated by silica gel flash chromatography, using first 7:3 ethyl acetate/hexane, then a 100:0 to 9:1 gradient of ethyl acetate/methanol. The less polar material, 0.071 g of 4-(2,4-dichloro-5-methoxyphenylamino)-7-methoxy-8-(2-[1,2,3]triazol-2-yl-ethoxy)benzo[g]quinoline-3-carbonitrile, is obtained as yellow solid, mp 285-287° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638929B2
出典データセットuspto-grants-2003_10
ORD IDord-077719d9d7764c5f9933c66d1f1cdf08
出典メモuspto-grants-2003_10