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HRID 537858作成日:2026年10月26日

Potassium Carbonate → N-(3-((5-(1H-indol-2-yl)oxazol-2-yl)amino)phenyl)methanesulfonamide

https://huagongshe.com/reaction/537858

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物tert-butyl 2-(2-((3-(methylsulfonamido) phenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylateHCID 71060239—
溶媒MethanolHCID 887—
溶媒Acetone hexaneHCID 21880519—
生成物N-(3-((5-(1H-indol-2-yl)oxazol-2-yl)amino)phenyl)methanesulfonamideHCID 7106047563.3%

反応手順

To a stirred solution of tert-butyl 2-(2-((3-(methylsulfonamido) phenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate 24 (0.221 g, 0.472 mmol) in methanol (30 mL) was added potassium carbonate (0.652 g, 4.71 mmol) at room temperature. Reaction mixture was refluxed for 2 hours. After completion of the reaction (as judged by TLC) it was concentrated using rotavapour and the crude product was purified by MPLC column chromatography (Biotage; Acetone/hexane as an eluent) to provide N-(3-((5-(1H-indol-2-yl)oxazol-2-yl)amino)phenyl)methanesulfonamide 25 (0.11 g, 63% yield) as a solid. MS (ES) m/z 369 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865709B2
出典データセットuspto-grants-2014_10
ORD IDord-0ffd9a9299384203b5673f1f7db540a1
出典メモuspto-grants-2014_10