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HRID 1096919作成日:2026年10月25日

Sodium Carbonate → 5-{1'-Tert-butoxycarbonyl-4-oxospiro[chroman-2,4'-piperidin]-6-yl}nicotinic acid tert-butyl ester

https://huagongshe.com/reaction/1096919

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5-{1'-Tert-butoxycarbonyl-4-oxospiro[chroman-2,4'-piperidin]-6-yl}nicotinic acid tert-butyl esterHCID 57930979—

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-nicotinicacid 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US08138197B2
出典データセットuspto-grants-2012_03
ORD IDord-83d3ee3b363d43a79f701da9cc9dbc7f
出典メモuspto-grants-2012_03