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HRID 62161作成日:2026年10月25日

Potassium Carbonate → 5-((3,6-dibromo-9H-carbazol-9-yl)methyl)-3-(pyridin-2-yl)oxazolidin-2-one

https://huagongshe.com/reaction/62161

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2-IodopyridineHCID 221126—
反応物Dichloromethane ethylacetateHCID 21226138—
反応物5-((3,6-dibromo-9H-carbazol-9-yl)methyl)oxazolidin-2-oneHCID 58097198—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物5-((3,6-dibromo-9H-carbazol-9-yl)methyl)-3-(pyridin-2-yl)oxazolidin-2-oneHCID 5809718579.4%

反応条件

温度130 °C

反応手順

A mixture of 5-((3,6-dibromo-9H-carbazol-9-yl)methyl)oxazolidin-2-one (0.0195 g, 0.0460 mmol), 2-iodopyridine (0.0209 g, 0.102 mmol), CuI (0.0009 g, 0.00460 mmol), and K2CO3 (0.0058 g, 0.0418 mmol) in 0.5 mL of DMSO was sealed tightly in a vial and heated at 130° C. for 12 hours. The reaction mixture was cooled and diluted with 20 mL EtOAc and washed with water 5×10 mL. The organic layer was dried over anhydrous Na2SO4 and evaporated to afford the crude product, which was subjected to silica gel chromatography using CH2Cl2/EtOAc as elute to afford 0.0183 g white solid as product, yield 79.4%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446022B2
出典データセットuspto-grants-2016_09
ORD IDord-1a2f3e48ac9242e69158fb9f21196acb
出典メモuspto-grants-2016_09