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HRID 13446作成日:2026年10月24日

Potassium Carbonate → Tert-butyl 4-(4-amino-3-nitrophenoxy)picolinate

https://huagongshe.com/ja/reaction/13446

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Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物4-Amino-3-NitrophenolHCID 3758882—
反応物tert-Butyl 4-chloropicolinateHCID 11806045—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-(4-amino-3-nitrophenoxy)picolinateHCID 22041090—

反応条件

温度80 °C

反応手順

Solid anhydrous white powdered KHMDS (2 eq) was suspended in a solution of dimethylformamide. Red crystalline 4-amino-3-nitrophenol (1 eq) was charged to the rapidly stirring solution under an inert atmosphere and the heterogeneous solution was allowed to stir for 2 hours. Then a dimethylformamide solution of tert-butyl 4-chloropyridine-2-carboxylate (1 eq) was added dropwise. Anhydrous powdered potassium carbonate (1.2 eq) was charged to the reaction as an acid scavenger. The purple colored viscous mixture was heated to 80° C. for 12-15 hours until when it was determined to be complete by HPLC. The reaction was evaporated under reduced pressure and diluted with excess ethyl acetate and water. An extraction of the aqueous layer was made with ethyl acetate. The organic layers were combined and washed 4 times with water followed by brine. The organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude material was purified by flash silica gel chromatography using an eluent of 1:1 mixture of hexanes to ethyl acetate to give the desired product. MS: MH+=332.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728010B2
出典データセットuspto-grants-2010_06
ORD IDord-00d13c5c1a234708ab4cef80b7b55f27
出典メモuspto-grants-2010_06