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HRID 1689768作成日:2026年10月25日

Potassium Phosphate, Tribasic → 5-(4-Hydroxy-piperidin-1-yl)-biphenyl-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1689768

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Phenylboronic AcidHCID 66827—
反応物2-Bromo-4-(4-hydroxy-piperidin-1-yl)-benzoic acid methyl esterHCID 66906453—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物5-(4-Hydroxy-piperidin-1-yl)-biphenyl-2-carboxylic acid methyl esterHCID 6690632892%

反応条件

温度90 °C

反応手順

A mixture of 2-bromo-4-(4-hydroxy-piperidin-1-yl)-benzoic acid methyl ester (1.2 g, 3.82 mmol), phenylboronic acid (800 mg; 6.56 mmol), potassium phosphate, tribasic, mono-hydrate (1.3 g, 10.7 mmol), and tetrakis(triphenylphosphine)palladium (500 mg, 0.433 mmol) in 1,2-dimethoxyethane (25 mL) and water (1 mL) is heated to 90° C. under a nitrogen atmosphere for 24 h. The mixture is concentrated and partitioned between ethyl acetate and water. The solvent layers are separated and the aqueous layer is extracted with ethyl acetate (3×). The combined ethyl acetate layers are dried (MgSO4), filtered, and concentrated under reduced pressure. The residue is purified on silica (120 g) eluting with a gradient of 0% to 100% ethyl acetate in heptane to provide the desired product (1.09 g, 92%) as a gummy residue. LC-ES/MS m/z 312.0 (M+1)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08153624B2
出典データセットuspto-grants-2012_04
ORD IDord-f9ea7e08183f46bbb506ea5e594752a3
出典メモuspto-grants-2012_04