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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595408생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/595408

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Oxalyl chlorideHCID 65578—
반응물Ethyl 2-amino-3-oxobutanoateHCID 13282896—
반응물Ethyl 6-chloro-4-(cyclobutylamino)nicotinateHCID 89689654—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoateHCID 89689546—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242975B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-c3669fc7dc7844b1b9e451f4f7af9d69
출처 메모uspto-grants-2016_01