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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38476생성일: 2026년 10월 24일

Water → Tert-Butyl 6-(1-methyl-1H-pyrazol-4-yl)-4-oxo-spiro[chroman-2,4'-piperidine]-1'-carboxylate

https://huagongshe.com/ko/reaction/38476

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
반응물tert-Butyl 6-bromo-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylateHCID 2794759—
촉매HCID 178418397HCID 178418397—
용매Sodium CarbonateHCID 10340—
용매1,4-DioxaneHCID 31275—
생성물Tert-Butyl 6-(1-methyl-1H-pyrazol-4-yl)-4-oxo-spiro[chroman-2,4'-piperidine]-1'-carboxylateHCID 57931011—

반응 조건

온도100 °C

반응 단계

tert-Butyl 6-bromo-4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate (1 g) and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (682 mg) were dissolved in dioxane in a nitrogen atmosphere, and aqueous 2M Na2CO3 (10 ml) solution (3.8 mL) and tetrakis(triphenylphosphine)palladium (144 mg) were added thereto, and degassed. The reaction liquid was stirred overnight at 100° C., cooled to room temperature, then water was added thereto, and filtered through Celite. The filtrate was extracted with chloroform, and the organic layer was dried with sodium sulfate. Sodium sulfate was removed through filtration, the filtrate was concentrated under reduced pressure, and the residue was purified through silica gel column chromatography (hexane/EtOAc) to obtain the intended compound as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524730B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-67eb52c178e84a9ea08b3ca34d24cc0a
출처 메모uspto-grants-2013_09