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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008112생성일: 2026년 10월 25일

Methanol → 3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/1008112

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indol-2-oneHCID 60111231—
생성물3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid methyl esterHCID 6011122363%

반응 단계

A reaction mixture of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-1-(imidazole-1-ylcarbonyl)-1,3-dihydro-indol-2-one (5.3 mg, 0.016 mmol) in 1.0 mL of methanol was stirred at room temperature for 64 h and filtered. The red solid was washed with methanol and dried in a vacuum oven overnight to afford 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid methyl ester (3.0 mg, 63%) as a red solid. 1H NMR (400 MHz, DMSO-d6) d 12.63 (s, 1H, NH-1′), 7.84-7.86 (m, 1H), 7.69 (s, 1H, H-vinyl), 7.56-7.68 (m, 1H), 7.19-7.22 (m, 2H), 6.06 (d, J=2.34 Hz, 1H, H-4′), 4.08 (s, 3H, OCH3), 2.40 (s, 3H, CH3), and 2.36 (s, 3H, CH3). MS m/z (relative intensity, %) 297 (100, [M+1]+.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06797725B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-4c315e8aaf294c57bf712b6f62f6fada
출처 메모uspto-grants-2004_09