関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Trifluoroacetic anhydride | HCID 9845 | — |
| 反応物 | Sodium Thiosulfate | HCID 24477 | — |
| 反応物 | Carbamide Peroxide | HCID 31294 | — |
| 反応物 | 6-Bromo-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole | HCID 58364943 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 6-Bromo-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-1,7-dioxide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09440976B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-8aa7c493f63b4a119f4e7f96471db558 |
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| 出典メモ | uspto-grants-2016_09 |
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