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HRID 269533作成日:2026年10月26日

Potassium Carbonate → 2-Benzyloxy-5''-butyrylamino-5-trifluoromethyl[1,1';2',1'']terphenyl-3''-carboxylic acid ethyl ester

https://huagongshe.com/reaction/269533

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Toluene ethanolHCID 21863594—
反応物2-Benzyloxy-5-trifluoromethylphenylboronic acidHCID 23005339—
反応物2'-Bromo-5-butyrylamino-biphenyl-3-carboxylic acid methyl esterHCID 69312113—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物2-Benzyloxy-5''-butyrylamino-5-trifluoromethyl[1,1';2',1'']terphenyl-3''-carboxylic acid ethyl esterHCID 5873098376%

反応条件

温度90 °C

反応手順

A mixture of 2-benzyloxy-5-trifluoromethyl-phenyl-boronic acid (38 mg, 0.13 mmol), 2′-bromo-5-butyrylamino-biphenyl-3-carboxylic acid methyl ester (45 mg, 0.12 mmol), potassium carbonate (138 mg, 1 mmol) and tetrakis(triphenylphosphine)palladium(0) (14 mg, 0.012 mmol) in 1:1 toluene/ethanol (3 ml) was stirred and heated at 90° C. under nitrogen for 2 hours. After cooling the mixture was diluted with diethyl ether and water and the organic phase dried (MgSO4) and evaporated to dryness. The residue was purified using Biotage with ethyl acetate/iso-hexane (1:4) to yield the title compound as a colourless gum (51 mg, 76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446222B2
出典データセットuspto-grants-2008_11
ORD IDord-a2455b2326d24ff885fe7230018b9ef0
出典メモuspto-grants-2008_11