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HRID 38478作成日:2026年10月25日

Sodium Carbonate → tert-Butyl 6-(5-carbamoylpyridin-2-yl)-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/38478

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物6-ChloronicotinamideHCID 80456—
反応物1'-Tert-butoxycarbonyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[chroman-2,4'-piperidin]-4-oneHCID 57930961—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒1,4-DioxaneHCID 31275—
生成物tert-Butyl 6-(5-carbamoylpyridin-2-yl)-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylateHCID 58208682—

反応条件

温度100 °C

反応手順

1′-tert-butoxycarbonyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[chroman-2,4′-piperidin]-4-one (40.0 g, 90.0 mmol), 6-chloronicotinamide (17.0 g, 108 mmol), Pd(PPh3)4 (5.21 g, 4.51 mmol), and aqueous 2M Na2CO3 (100 ml) solution were suspended in dioxane (300 ml) and heated at 100° C. for 16 h. The reaction mixture was diluted with CHCl3 and H2O, the aqueous layer was extracted with CHCl3. The combined organic layer was washed with brine, dried over MgSO4 and silicagel. The desiccant was removed through celite filtration and the filtrate was concentrated under reduced pressure. The resulting residue was purified by crystallization (CHCl3-EtOAc) to obtain the intended compound as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524730B2
出典データセットuspto-grants-2013_09
ORD IDord-71529f5fb4fa4deb990dc0de44b47136
出典メモuspto-grants-2013_09