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HRID 379187作成日:2026年10月27日

rel-(2R,6S)-2,6-Dimethylpiperidine → 4-(2,6-Dimethyl-piperidin-1-yl)-but-2-enoic acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amide

https://huagongshe.com/reaction/379187

反応式

関与物質

役割名称HCID仕込み量
反応物rel-(2R,6S)-2,6-DimethylpiperidineHCID 641768—
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—
溶媒Sodium BicarbonateHCID 516892—
生成物4-(2,6-Dimethyl-piperidin-1-yl)-but-2-enoic acid[4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-methoxy-quinolin-6-yl]-amideHCID 6720330564%

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 137 μL (1.02 mmol) of cis-2,6-dimethylpiperidine in 2.25 ml dimethylformamide was stirred at room temperature for 3 hr. The reaction mixture was diluted with saturated sodium bicarbonate solution and extracted with ethyl acetate. The extracts were evaporated to an oil, washed with hexane and dried under reduced pressure to yield 170.4 mg (64%) tan solid: mp 120-122° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297258B1
出典データセットuspto-grants-2001_10
ORD IDord-1e96455f108345b88e551ec11fe4d0f1
出典メモuspto-grants-2001_10