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HRID 3205作成日:2026年10月24日

4-Ethoxyaniline → 6-(2,6-Dichlorophenyl)-2-(4-ethoxyphenylamino)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/ja/reaction/3205

反応式

関与物質

役割名称HCID仕込み量
反応物4-EthoxyanilineHCID 9076—
反応物6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 10596994—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物6-(2,6-Dichlorophenyl)-2-(4-ethoxyphenylamino)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11619422—

反応手順

A mixture of 0.150 g (0.38 mmol) of 6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 68 and 0.500 g (3.60 mmol) of 4-ethoxyaniline was fused in a 160° C. oil bath for 10 minutes. The dark violet melt was cooled and dissolved in 1 mL of warm glacial acetic acid. This solution was diluted to 10 mL volume with water to precipitate a solid. The solid was filtered, washed well with water, and dried; wt 0.140 g. Purification was effected by filtration of an ethyl acetate solution through a layer of silica gel and washing the silica gel with ethyl acetate. The filtrate was concentrated to 2 mL volume and 2 mL of petroleum ether was added. The crystals that separated on inducement were filtered and washed with ether; wt 0.094 g; mp 192°-194° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733914
出典データセットuspto-grants-1998_03
ORD IDord-e03019db057645d990f6974409cc35bc
出典メモuspto-grants-1998_03