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HRID 2213842作成日:2026年10月27日

Potassium Phosphate, Tribasic → 8-(Benzyloxy)-4-[(2-chloro-4-fluoro-5-methoxyphenyl)amino]-7-methoxybenzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/2213842

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
反応物8-(Benzyloxy)-4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrileHCID 21956464—
反応物2-Chloro-4-fluoro-5-methoxybenzenamineHCID 21956478—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物8-(Benzyloxy)-4-[(2-chloro-4-fluoro-5-methoxyphenyl)amino]-7-methoxybenzo[g]quinoline-3-carbonitrileHCID 1016466136%

反応条件

温度80 °C

反応手順

A mixture of 8-(benzyloxy)-4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrile (1.00 g, 2.7 mmol), 2-chloro-4-fluoro-5-methoxyaniline (560 mg, 3.2 mmol), tris(dibenzylideneacetone)dipalladium(0) (240 mg, 0.26 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (330 mg, 0.84 mmol) and K3PO4 (860 mg, 4.1 mmol) in 15 mL of ethylene glycol dimethyl ether is heated at 80° C. for 3 hours. An additional 5% of all reagents is added and the mixture is heated at 80° C. for 2 hours then cooled to room temperature and partitioned between aqueous sodium bicarbonate and methylene chloride. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by column chromatography eluting with 1:1 hexane/ethyl acetate yields 500 mg (36%) of 8-(benzyloxy)-4-[(2-chloro-4-fluoro-5-methoxyphenyl)amino]-7-methoxybenzo[g]quinoline-3-carbonitrile as a yellow solid, mp 248–250° C. dec.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07105531B2
出典データセットuspto-grants-2006_09
ORD IDord-5761a33390cf4c2383139b40e1bb498a
出典メモuspto-grants-2006_09