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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38465생성일: 2026년 10월 25일

Pyridine → Methyl 4-(3-methyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4'-piperidin]-1'-yl]carbonyl}-1H-indazol-1-yl)benzoate

https://huagongshe.com/reaction/38465

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-Methoxycarbonylphenylboronic acidHCID 2734369—
반응물HCID 178434311HCID 178434311—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
생성물Methyl 4-(3-methyl-6-{[6-(1-methyl-1H-pyrazol-4-yl)-4-oxospiro[chroman-2,4'-piperidin]-1'-yl]carbonyl}-1H-indazol-1-yl)benzoateHCID 58208718—

반응 단계

Pyridine (0.080 ml, 0.988 mmol) was added to a stirred mixture of 1′-[(3-methyl-1H-indazol-6-yl)carbonyl]-6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4′-piperidin]-4-one (150 mg, 0.329 mmol), [4-(methoxycarbonyl)phenyl]boronic acid (119 mg, 0.659 mmol), Cu(OAc)2 (90 mg, 0.494 mmol) in CH2Cl2 (1.5 ml) and the mixture was stirred at room temperature overnight. The mixture was filtered and the solvent was evaporated under reduced pressure. The residue was purified by silicagel column chromatography (hexane/EtOAc) to give intended compound as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524730B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-237c1c2aa4ad44cba971796595c3eaf1
출처 메모uspto-grants-2013_09