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HRID 639006作成日:2026年10月26日

1,2-Dimethoxyethane → 6-Methoxy-4-vinyl-quinoline

https://huagongshe.com/reaction/639006

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Potassium CarbonateHCID 11430—
反応物6-Methoxy-1,5-naphthyridin-4-yl trifluoromethanesulfonateHCID 11255265—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物6-Methoxy-4-vinyl-quinolineHCID 5902621881%

反応手順

To a solution of 6-(methyloxy)-1,5-naphthyridin-4-yl trifluoromethanesulfonate (5.0 g, 16.23 mmol) in DME (80 mL) and H2O (40 mL) was added trivinyl boronate (1.96 g, 8.1 mmol), K2CO3 (2.23 g, 16.23 mmol) and Pd(PPh3)4 (0.19 g, 0.16 mmol). After 3 h at 90° C. under N2, the reaction solution was concentrated under vacuum and purified on silica (hexane/EtOAc, 4:1) to give the title compound as a yellow oil (2.44 g, 81%): LC/MS (m/z) (ES) 186 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691850B2
出典データセットuspto-grants-2010_04
ORD IDord-7439aa1200dc4475801e0bcb450a3233
出典メモuspto-grants-2010_04