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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49557생성일: 2026년 10월 24일

Ethyl Acetate → 4-(Aminosulfonyl)-N-{(cis)-2-[({[(3-chlorophenyl)sulfonyl]amino)acetyl)amino]cyclohexyl}benzamide

https://huagongshe.com/ko/reaction/49557

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물3-Chlorobenzenesulphonyl chlorideHCID 17909—
반응물N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromideHCID 68830145—
용매DimethylformamideHCID 6228—
생성물4-(Aminosulfonyl)-N-{(cis)-2-[({[(3-chlorophenyl)sulfonyl]amino)acetyl)amino]cyclohexyl}benzamideHCID 6882806829.4%

반응 단계

N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide, (61b), (70 mg) was dissolved in DMF (2.5 mL) prior to the addition of 3-chlorobenzenesulfonyl chloride (51 mg). After stirring overnight, EtOAc was added and the solution was washed with 1N HCl. The EtOAc was dried, filtered, and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title benzamide (25 mg). MS found: (M+H)+=530.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706712B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-dcc707d7869046489fcea5627c8f95db
출처 메모uspto-grants-2004_03