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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1828280생성일: 2026년 10월 26일

5-Fluoroindole-2-carboxylic acid → 5-fluoro-2-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}-1H-indole

https://huagongshe.com/reaction/1828280

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참여 물질

역할이름HCID투입량
반응물5-Fluoroindole-2-carboxylic acidHCID 1820—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-(2-Pyridyl)piperazineHCID 94459—
용매DichloromethaneHCID 6344—
생성물5-fluoro-2-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}-1H-indoleHCID 22065982—

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온도25 °C

반응 단계

5-Fluoro-1H-indole-2-carboxylic acid (4.0 g) and EDCI (4.29 g) were combined in dichloromethane (90 mL) and treated with 1-(2-pyridinyl)piperazine (3.64 g). After stirring at 25° C. for 24 hours, the mixture was washed with 150 mL of water and filtered. The filter cake was washed in succession with 300 mL of water, 250 mL of dichloromethane and 20 mL of ethyl acetate to provide the title compound. 1H NMR (d6-DMSO, 300 MHz) δ 3.61 (m, 4H), 3.85 (m, 4H), 6.67 (dd, 1H, J=7.5, 4.8 Hz), 6.85 (m, 2H), 7.06 (m, 1H), 7.40 (m, 2H), 7.65 (m, 1H), 8.04 (dd, 1H, J=4.5, 1.8 Hz), 11.72 (bs, 1H). MS (DCI/NH3) m/z 325 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07057042B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-a44d2f7e66fb4833ab5fe2e067712ffc
출처 메모uspto-grants-2006_06