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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79093생성일: 2026년 10월 23일

Benzenesulfonamide, 3-amino- → 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide

https://huagongshe.com/ko/reaction/79093

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonamide, 3-amino-HCID 7377—
반응물Thionyl ChlorideHCID 24386—
반응물2-(4-Fluorophenoxy)-4-tert-butylbenzoic acidHCID 58988089—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamideHCID 2485521150%

반응 단계

A solution of 2-(4-fluorophenoxy)-4-tert-butylbenzoic acid (0.11 g, 0.39 mmol) and thionyl chloride (0.28 mL, 3.9 mmol) in CH2Cl2 (10 mL) was stirred at room temperature for 4 h. The solvent was evaporated under reduced pressure, and to the resulting oil was added a solution of 3-amino-benzenesulfonamide (73 mg, 0.42 mmol) in pyridine (4 mL). The solution was stirred at room temperature 15 h. The reaction was diluted with water and extracted with EtOAc. The combined extracts were washed with water, dried over Na2SO4, and evaporated under reduced pressure. The residue was purified by silica gel chromatography (0%-50% EtOAc-hexanes) to obtain a white solid which was recrystallized from EtOAc and hexanes. 2-(4-Fluorophenoxy)-4-tert-butyl-N-(3-(aminosulfonyl)phenyl)benzamide (85 mg, 50% yield) was obtained as a white solid. LC/MS: m/z 443.3 (M+H)+ at 3.49 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-9f3311df790543d0b65bf661b6c85066
출처 메모uspto-grants-2014_09