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HRID 420153作成日:2026年10月25日

Sodium Carbonate → 3-Pyridinecarboxylic acid, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/420153

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tert-Butyl 6-bromo-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylateHCID 2794759—
反応物tert-Butyl 5-bromonicotinateHCID 18422124—
反応物HCID 178476685HCID 178476685—
触媒palladium(II) acetateHCID 167845—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物3-Pyridinecarboxylic acid, 1,1-dimethylethyl esterHCID 182484—

反応条件

温度100 °C

反応手順

tert-butyl-6-bromo-4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate (19.8 g, 50.0 mmol), bis(pinacolato)diboran (14.0 g, 55.0 mmol), Pd(OAc)2 (560 mg, 2.50 mmol), DPPF (2.77 g, 5.00 mmol), and AcOK (5.82 g, 60.0 mmol) were suspended in dioxane (250 mL) and heated at 100° C. for 10 hours. After cooling down to room temperature, 5-bromo-nicotinic acid tert-butyl ester (14.2 g, 55.0 mmol), Pd(PPh3)4 (5.78 g, 5.00 mmol) and 2M Na2CO3 aq. (125 mL, 250 mmol) were added to the reaction mixture; and then heated at 100° C. for 15 hours. The reaction mixture was diluted with EtOAc and H2O, organic layer was washed with brine and dried over MgSO4. After filtration, the solvents were removed in vacuo and the residue was purified by silica gel column chromatography (hexane/EtOAc=10/0 to 6/4) and the obtained brown solid was crystallized from EtOAc/hexane (1/1) to afford 5-{1′-tert-butoxycarbonyl]-4-oxospiro[chroman-2,4′-piperidin]-6-yl}nicotinic acid tert-butyl ester as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093389B2
出典データセットuspto-grants-2012_01
ORD IDord-7d3fb9ad22a1491aab38b03b5b47e941
出典メモuspto-grants-2012_01