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HRID 548491作成日:2026年10月24日

Diisopropanolamine → 4-[Bis-(2-hydroxy-propyl)-amino]-but-2-enoic Acid [4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide

https://huagongshe.com/ja/reaction/548491

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropanolamineHCID 8086—
反応物Sodium BicarbonateHCID 516892—
反応物4-Bromo-but-2-enoic acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amideHCID 54242075—
溶媒DimethylformamideHCID 6228—
生成物4-[Bis-(2-hydroxy-propyl)-amino]-but-2-enoic Acid [4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amideHCID 67203530—

反応条件

温度60 °C

反応手順

A mixture of 250 mg (0.51 mmol) of 4-bromo-but-2-enoic acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide, and 136 mg (1.02 mmol) of 1,1′-iminodi-2-propanol in 2.25 ml dimethylformamide was stirred at room temperature for 3 hr and at 60° C. for 2 hr. After the mixture was cooled, saturated sodium bicarbonate solution was added and the solution was subsequently extracted with ethyl acetate. The extracts were evaporated to an oil, washed with hexane and dried under reduced pressure. Yield 240.1 mg (87%) tan solid: mp 122-125° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE042376E1
出典データセットuspto-grants-2011_05
ORD IDord-757843ad5fbd4d8d9f872cc0a8b39990
出典メモuspto-grants-2011_05