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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1008117생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1008117

반응식

참여 물질

역할이름HCID투입량
반응물Glycolic AcidHCID 757—
반응물Trifluoroacetic acidHCID 6422—
반응물3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indol-2-oneHCID 60111231—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid carboxymethyl esterHCID 6011123925%

반응 단계

A reaction mixture of 3-[1-(3,5-dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indole-2-one (166 mg, 0.5 mmol), glycolic acid (163 mg, 1.5 mmol, 70% w/w in water) and (68 mg, 0.6 mmol) of TFA in 3 mL of THF was stirred at room temperature for 4 h and diluted with ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated. The precipitate was filtered, washed with small amount of ethyl acetate, and dried in a vacuum oven overnight to afford 42 mg (25%) of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid carboxymethyl ester. 1H NMR (400 MHz, DMSO-d6 and CDCl3) δ 12.63 (s, 1H, NH-1′), 7.92-7.94 (m, 1H), 7.52-7.55 (m, 1H), 7.44 (s, 1H, H-vinyl), 7.20-7.22 (m, 2H), 6.06 (s, br, 1H, H-4′), 4.94 (s, 2H, CH2), 2.39 (s, 3H, CH3), and 2.36 (s, 3H, CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06797725B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-7a9e387b26254a40a7d38ce38e01aa46
출처 메모uspto-grants-2004_09