Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131130생성일: 2026년 10월 26일
Triethylamine → (S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-furan-2-carboxamide
https://huagongshe.com/reaction/131130
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Furancarbonyl chloride | HCID 68242 | — |
| 반응물 | (S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyran | HCID 11139461 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-furan-2-carboxamide | HCID 54000140 | 79% |
반응 단계
To an ice-cooled stirred solution of (S)-3-amino-5-(4-methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (230 mg, 0.930 mmol) and triethylamine (194 μL, 1.39 mmol) in anhydrous methylene chloride (10 mL) was added 2-furoyl chloride (101 μL, 1.02 mmol) under nitrogen. The ice-bath was removed, and the reaction mixture was allowed to reach room temperature. The mixture was washed with a 2 M NH3 solution, dried (MgSO4), and the solvent was removed in vacuo. The remains was purified on a chromatotron (accelerated thin layer chromatography, eluent: chloroform/ethanol; 92:8+0.5% conc. NH3) affording 249 mg (79% yield) of the title compound as a white solid: mp sinters >50° C.; [α]21D −83° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 341 (52, M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07384943B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-3ce034501a3d408493e9e56ce94ee367 |
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| 출처 메모 | uspto-grants-2008_06 |
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