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HRID 877549作成日:2026年10月25日

4-Methylmorpholine → Ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate

https://huagongshe.com/reaction/877549

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物Oxalyl chlorideHCID 65578—
反応物Ethyl 2-amino-3-oxobutanoateHCID 13282896—
反応物Ethyl 6-chloro-4-(cyclobutylamino)nicotinateHCID 89689654—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoateHCID 89689546—

反応手順

A stirred solution of 6-chloro-4-(isopropylamino)nicotinic acid (2) in DCM (15 mL) was cooled to 0° C., oxalyl chloride (2 equiv) was added, followed by addition of 2 drops of DMF. The reaction mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated to remove excess of oxalyl chloride. The acyl chloride, generated in-situ was dissolved in THF and added dropwise to a cool, stirred solution of ethyl 2-amino-3-oxobutanoate (1.1 equiv.) and NMM (5 equiv.) in THF. The reaction temperature was slowly brought to room temperature and stirred overnight. The reaction mixture was diluted with EtOAc and washed with water, followed by brine solution. The EtOAc layer was collected, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by column chromatography through silica gel and EtOAc: Pet. Ether as eluent to afford the title compound, ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987311B2
出典データセットuspto-grants-2015_03
ORD IDord-f83adc0c7b71415f8695f48a52bea506
出典メモuspto-grants-2015_03