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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60315생성일: 2026년 10월 25일

Water → 6-Bromo-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-1,7-dioxide

https://huagongshe.com/reaction/60315

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Sodium ThiosulfateHCID 24477—
반응물Carbamide PeroxideHCID 31294—
반응물6-Bromo-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4',3'-d]pyrroleHCID 58364943—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물6-Bromo-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-1,7-dioxideHCID 86656044—

반응 단계

To a suspension of hydrogen peroxide-urea adduct (4.2 g, 45 mmol) in chloroform (37 mL) was added trifluoroacetic anhydride (6.3 mL, 44.4 mmol) dropwise over 10 minutes. The reaction mixture was stirred at ambient temperature for 5 minutes and then to this was added 6-bromo-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole (2.1 g, 5.6 mmol) as a solution in chloroform (15 mL). Note: an exotherm is observed upon addition of the substrate. The reaction mixture was stirred at ambient temperature for 10 minutes and then at 50° C. for 30 minutes. The reaction mixture was cooled to ambient temperature, treated with saturated sodium thiosulfate solution (20 mL), and diluted with water (50 mL) and methanol (10 mL). The layers were separated and the organic layer was washed with 0.5N hydrochloric acid (50 mL), dried over sodium sulfate, filtered, concentrated in vacuo, and purified by flash chromatography (silica, 80 g, ISCO, 0-10% methanol in dichloromethane) to afford the title compound as a pale yellow solid, which was used in the next step without any further purification (1 g, 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440976B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8aa7c493f63b4a119f4e7f96471db558
출처 메모uspto-grants-2016_09