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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1749753생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1749753

반응식

참여 물질

역할이름HCID투입량
반응물7-Benzyloxyindole-3-carbaldehydeHCID 260799—
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-[(2-{[7-(benzyloxy)-1H-indol-3-yl]methylene}-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylateHCID 8668194961%

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 7-benzyloxy-1H-indole-3-carboxaldehyde (0.035 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 reaction mixture was cooled to room temperature, and then the solid was collected by filtration, and washed with a mixed solvent of chloroform and methanol to obtain tert-butyl (Z)-4-[(2-{[7-(benzyloxy)-1H-indol-3-yl]methylene}-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate (0.049 g, 61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156827B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-12d34e4167c14099a73a59284ab9c630
출처 메모uspto-grants-2015_10