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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glycolic Acid | HCID 757 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-1-(imidazol-1-ylcarbonyl)-1,3-dihydro-indol-2-one | HCID 60111231 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid carboxymethyl ester | HCID 60111239 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06797725B2 |
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| 출처 데이터셋 | uspto-grants-2004_09 |
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| ORD ID | ord-7a9e387b26254a40a7d38ce38e01aa46 |
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| 출처 메모 | uspto-grants-2004_09 |
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