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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Indole-3-Carboxaldehyde | HCID 10256 | — |
| 반응물 | Tert-butyl 4-[(5-chloro-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate | HCID 71278506 | — |
| 촉매 | Piperidine | HCID 8082 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 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 | HCID 86681911 | 85% |
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
| 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-45bfa1da8a8c46b4bf163930c1e04c57 |
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| 출처 메모 | uspto-grants-2015_10 |
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