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HRID 79095생성일: 2026년 10월 24일

Benzenesulfonamide, 3-amino- → 2-cyclohexyl-N-(3-(aminosulfonyl)phenyl)benzamide

https://huagongshe.com/ko/reaction/79095

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonamide, 3-amino-HCID 7377—
반응물TriethylamineHCID 8471—
반응물2-cyclohexylbenzoic AcidHCID 7020572—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물2-cyclohexyl-N-(3-(aminosulfonyl)phenyl)benzamideHCID 24855264—

반응 단계

A solution of 2-cyclohexyl benzoic acid (20 mg, 0.10 mmol) and HATU (38 mg, 0.10 mmol) in DMF (1 mL) was stirred at room temperature 3 min. To this solution was added 3-amino-benzenesulfonamide (17 mg, 0.10 mmol) and triethylamine (14 μL, 0.10 mmol). The reaction was stirred at room temperature for 16 h and purified by preparative reverse phase HPLC using 10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA) to give 2-cyclohexyl-N-(3-(aminosulfonyl)phenyl)benzamide. LC/MS: m/z 359.1 (M+H)+ at 3.85 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841483B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7c0b71d177244859a5b82e65e13df75e
출처 메모uspto-grants-2014_09