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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Furancarbonyl chlorideHCID 68242—
반응물(S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyranHCID 11139461—
용매DichloromethaneHCID 6344—
생성물(S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-furan-2-carboxamideHCID 5400014079%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384943B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-3ce034501a3d408493e9e56ce94ee367
출처 메모uspto-grants-2008_06