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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1159478생성일: 2026년 10월 27일

p-Toluenesulfonic acid → 7-trifluoromethyl-10H-benzo(4,5)furo(3,2-b)indole-1-carboxylic acid

https://huagongshe.com/reaction/1159478

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2-Hydrazinobenzoic acidHCID 79223—
반응물2-[N'-(6-trifluoromethyl-benzofuran-3-yl-idene)-hydrazino]-benzoic acidHCID 131728372—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물7-trifluoromethyl-10H-benzo(4,5)furo(3,2-b)indole-1-carboxylic acidHCID 6844661064.4%

반응 단계

150 mg 6a was dissolved in ethanol (5.2 ml) and 2-hydrazino benzoic acid was dissolved in water (10.3 ml). These two homogenous mixtures were mixed together and stirred at room temperature for 4 hrs. Precipitation is filtered and first washed with water and then ethanol. The filtrate was put in vacuum oven for 4 hrs for complete evaporation. The mixture of 2-[N′-(6-trifluoromethyl-benzofuran-3-yl-idene)-hydrazino]-benzoic acid (120 mg), p-TsOH (1˜2 Eqv) and ethanol (5 ml) were refluxed for 30 hrs. Cooled to room temperature and evaporated in vacuo. Resulting mixture was purified by chromatography to afford compound 8 (CHCl3:MeOH=30:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07812177B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-c31527f520d649d58963ffdb40578fc3
출처 메모uspto-grants-2010_10