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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 7-Benzyloxyindole-3-carbaldehyde | HCID 260799 | — |
| 반응물 | Tert-butyl 4-[(6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate | HCID 60155786 | — |
| 촉매 | Piperidine | HCID 8082 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 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 | HCID 86681949 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09156827B2 |
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| 출처 데이터셋 | uspto-grants-2015_10 |
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| ORD ID | ord-12d34e4167c14099a73a59284ab9c630 |
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| 출처 메모 | uspto-grants-2015_10 |
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