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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131131생성일: 2026년 10월 26일

Pyrrole-2-Carboxylic Acid → (S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-pyrrole-2-carboxamide

https://huagongshe.com/reaction/131131

반응식

참여 물질

역할이름HCID투입량
반응물Pyrrole-2-Carboxylic AcidHCID 12473—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물(S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyranHCID 11139461—
용매DimethylformamideHCID 6228—
생성물(S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-pyrrole-2-carboxamideHCID 53829301—

반응 조건

온도75 °C

반응 단계

A mixture of 1,1′-carbonyldiimidazole (360 mg, 1.85 mmol) and pyrrole-2-carboxylic acid (225 mg, 2.03 mmol) in anhydrous N,N-dimethylformamide (8 mL) was stirred at 75° C. for 45 min. The mixture was allowed to cool, and a solution of (S)-3-amino-5-(4-methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (457 mg, 1.85 mmol) in N,N-dimethylformamide (10 mL) was added. The reaction mixture was stirred for 7 days at room temperature under nitrogen. The solvent was removed in vacuo, and the residue was extracted with diethyl ether (50 mL) and water (20 mL). The aqueous layer was extracted with another portion of diethyl ether (50 mL). The combined ethereal layers were dried (MgSO4), and the solvent was removed in vacuo. The residue was purified by column chromatography on silica (eluent: chloroform/ethanol; 90:10+0.5% conc. NH3) yielding the title compound as an oil. Evaporation with diethyl ether afforded 300 mg (48% yield) of the title compound as a white powder: mp sinters >96° C.; [α]21D −82.8° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 340 (10, M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384943B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-4f9bb2b1e969495d8c502cd793f1910e
출처 메모uspto-grants-2008_06