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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49556생성일: 2026년 10월 24일

4-Methylmorpholine → 4-(Aminosulfonyl)-N-((cis)-2-{[({[2-(trifluoromethyl)anilino]carbonyl)amino)acetyl]amino}cyclohexyl)benzamide

https://huagongshe.com/ko/reaction/49556

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Ethyl AcetateHCID 8857—
반응물2-(Trifluoromethyl)phenyl isocyanateHCID 16794—
반응물N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromideHCID 68830145—
용매DimethylformamideHCID 6228—
생성물4-(Aminosulfonyl)-N-((cis)-2-{[({[2-(trifluoromethyl)anilino]carbonyl)amino)acetyl]amino}cyclohexyl)benzamideHCID 68826663—

반응 단계

N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide, (61b), (100 mg) was dissolved in DMF (3 mL) prior to the addition of 4-methylmorpholine (0.13 mL) and 2-trifluoromethylphenyl isocyanate (0.05 mL). 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 (50 mg). MS found: (M+Na)+=564.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706712B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-548d4312cc224e57adc1d3f3ab1ca060
출처 메모uspto-grants-2004_03