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HRID 883933作成日:2026年10月27日

Potassium Carbonate → {4-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenoxy]phenyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/883933

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N-(4-bromophenyl)-4-chloro-3-nitrobenzamideHCID 1068537—
反応物N-Boc-4-hydroxyanilineHCID 2756771—
溶媒DimethylformamideHCID 6228—
生成物{4-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenoxy]phenyl}-carbamic acid tert-butyl esterHCID 6704070297%

反応手順

A solution of the product of Example 49A (5.132 g, 14.45 mmol) in anhydrous N,N-dimethylformamide (50 mL) was treated with N-Boc-4-hydroxyaniline (3.024 g, 14.45 mmol) and potassium carbonate (3.994 g, 28.90 mmol) at room temperature, then heated at 80° under a nitrogen atmosphere for 4.5 hours. The reaction was cooled to room temperature and the solvent removed by rotary evaporation in vacuo. The residue was taken up in ethyl acetate (200 mL) and washed with water (4×50 mL) and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation to give the product as a dark yellow solid (7.38 g, 13.97 mmol, 97%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236950B2
出典データセットuspto-grants-2012_08
ORD IDord-a7be614b71074b4c82002c5fa57d3b7c
出典メモuspto-grants-2012_08