돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79101생성일: 2026년 10월 23일

Benzenesulfonamide, 3-amino- → 2-(2-Methylpyridin-3-yloxy)-n-(3-sulfamoylphenyl)-4-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/79101

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonamide, 3-amino-HCID 7377—
반응물TriethylamineHCID 8471—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-(2-methylpyridin-3-yloxy)-4-(trifluoromethyl)benzoic acid TFA saltHCID 131731884—
용매DimethylformamideHCID 6228—
생성물2-(2-Methylpyridin-3-yloxy)-n-(3-sulfamoylphenyl)-4-(trifluoromethyl)benzamideHCID 24855375—

반응 단계

A solution of 2-(2-methylpyridin-3-yloxy)-4-(trifluoromethyl)benzoic acid TFA salt (54 mg, 0.13 mmol) and HATU (50 mg, 0.13 mmol) in DMF (1 mL) was stirred at room temperature 3 min. To this solution was added 3-amino-benzenesulfonamide (23 mg, 0.13 mmol) and triethylamine (46 μL, 0.33 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-(2-methylpyridin-3-yloxy)-N-(3-sulfamoylphenyl)-4-(trifluoromethyl)benzamide. LC/MS: m/z 452.3 (M+H)+ at 1.07 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-9921ceb924de4fe59aebfb9a00a89807
출처 메모uspto-grants-2014_09