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HRID 60315作成日:2026年10月26日

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

https://huagongshe.com/reaction/60315

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物Sodium ThiosulfateHCID 24477—
反応物Carbamide PeroxideHCID 31294—
反応物6-Bromo-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4',3'-d]pyrroleHCID 58364943—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物6-Bromo-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-1,7-dioxideHCID 86656044—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440976B2
出典データセットuspto-grants-2016_09
ORD IDord-8aa7c493f63b4a119f4e7f96471db558
出典メモuspto-grants-2016_09