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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38478생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/38478

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물6-ChloronicotinamideHCID 80456—
반응물1'-Tert-butoxycarbonyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[chroman-2,4'-piperidin]-4-oneHCID 57930961—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매1,4-DioxaneHCID 31275—
생성물tert-Butyl 6-(5-carbamoylpyridin-2-yl)-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylateHCID 58208682—

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524730B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-71529f5fb4fa4deb990dc0de44b47136
출처 메모uspto-grants-2013_09