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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446676생성일: 2026년 10월 25일

Bromoacetic Acid → 2-bromo-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide

https://huagongshe.com/reaction/446676

반응식

참여 물질

역할이름HCID투입량
반응물Bromoacetic AcidHCID 6227—
반응물DiisopropylcarbodiimideHCID 12734—
반응물3-amino-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamideHCID 57448448—
용매DichloromethaneHCID 6344—
생성물2-bromo-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamideHCID 59249165—

반응 단계

In a 50 mL round-bottom flask was added 2-bromoacetic acid (1.87 g, 13.5 mmol), N,N-diisopropylcarbodiimide (860 mg, 6.8 mmol) and 10 mL DCM. To this mixture was added 3-amino-N-(3-(3,5-dimethoxyphenylamino) quinoxalin-2-yl)benzenesulfonamide (2.03 g, 4.5 mmol), prepared using procedures similar to those in Example 168. The reaction was stirred overnight at room temperature. Complete consumption of the starting aniline was confirmed by LCMS. The solvent was evaporated off to yield the crude product (2-bromo-N-(3-(N-(3-(3,5-dimethoxyphenylamino) quinoxalin-2-yl)sulfamoyl)phenyl)acetamide). This was used directly in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481001B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-eaaaffb0510a425db7412b110e21ab18
출처 메모uspto-grants-2013_07