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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1749749생성일: 2026년 10월 25일

6-nitro-1H-indole-3-carbaldehyde → tert-butyl (Z)-4-({6-hydroxy-2-[(6-nitro-1H-indol-3-yl)methylene]-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1749749

반응식

참여 물질

역할이름HCID투입량
반응물6-nitro-1H-indole-3-carbaldehydeHCID 5210076—
반응물Tert-butyl 4-[(6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylateHCID 60155786—
촉매PiperidineHCID 8082—
용매MethanolHCID 887—
생성물tert-butyl (Z)-4-({6-hydroxy-2-[(6-nitro-1H-indol-3-yl)methylene]-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylateHCID 8668194367.2%

반응 조건

온도50 °C

반응 단계

A solution of tert-butyl 4-[(6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate (0.050 g, 0.14 mmol) obtained in Example A16, Step 1 in methanol (2.0 mL) was added with 6-nitro-1H-indole-3-carboxaldehyde (0.026 g, 0.14 mmol). Then, the mixture was added with 5 drops of piperidine, and the mixture was stirred at 50° C. for 2 hours. The solvent was evaporated under reduced pressure, and then the residue was washed with a mixed solvent of chloroform and methanol to obtain tert-butyl (Z)-4-({6-hydroxy-2-[(6-nitro-1H-indol-3-yl)methylene]-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate (0.049 g, 67%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156827B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-93efc5fa26ca4ff480ff4669246daba9
출처 메모uspto-grants-2015_10