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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1749712생성일: 2026년 10월 26일

Indole-3-Carboxaldehyde → tert-butyl (Z)-4-({2-[(1H-indol-3-yl)methylene]-5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1749712

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-CarboxaldehydeHCID 10256—
반응물Tert-butyl 4-[(5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylateHCID 71278506—
촉매PiperidineHCID 8082—
용매MethanolHCID 887—
생성물tert-butyl (Z)-4-({2-[(1H-indol-3-yl)methylene]-5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylateHCID 8668191185%

반응 조건

온도40 °C

반응 단계

A solution of tert-butyl 4-[(5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate (0.014 g, 0.037 mmol) in methanol (2.0 mL) was added with 1H-indole-3-carboxaldehyde (0.013 g, 0.090 mmol). Then, the mixture was added with 5 drops of piperidine, and then the mixture was stirred at 40° C. for 2 hours. The reaction mixture was cooled to room temperature, and then the solid was collected by filtration, and washed with methanol to obtain tert-butyl (Z)-4-({2-[(1H-indol-3-yl)methylene]-5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate (0.016 g, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156827B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-45bfa1da8a8c46b4bf163930c1e04c57
출처 메모uspto-grants-2015_10