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HRID 238267作成日:2026年10月26日

Cesium carbonate → tert-butyl 4-(2-cyanophenyl)-5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/238267

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物2-Cyanophenylboronic acidHCID 2734610—
反応物Tert-butyl 4-(trifluoromethanesulfonyloxy)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 10991161—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物tert-butyl 4-(2-cyanophenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 1832659251.6%

反応条件

温度120 °C

反応手順

4-Trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (0.5 g, 1.5 mmol), 2-cyanophenylboronic acid (0.23 g, 1.6 mmol), tetrakis-triphenylphosphine (0.17 g, 0.15 mmol) and cesium carbonate (0.73 g, 2.26 mmol) were dissolved in a mixture of DME (3 mL), IMS (1.0 mL) and water (0.4 mL) under argon. The mixture was heated by microwave irradiation to 120° C. for 0.3 hours then diluted with water. The products were extracted into DCM, dried over magnesium sulphate, filtered and the solvent removed by evaporation under vacuum. The residue was purified by flash chromatography on silica eluting with 0-20% ethyl acetate/hexane. The fractions containing the desired product were concentrated under vacuum to give the title compound as a yellow oil (0.22 g). LCMS m/z 261.2 [M+H]+. R.T.=4.59 min (Analytical Method 4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642621B2
出典データセットuspto-grants-2014_02
ORD IDord-1a6eb3fef2f14ed88af10f8a85558141
出典メモuspto-grants-2014_02