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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349864생성일: 2026년 10월 25일

5-fluoro-1,3-dihydro-2H-indol-2-one → 5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

https://huagongshe.com/reaction/349864

반응식

참여 물질

역할이름HCID투입량
반응물5-fluoro-1,3-dihydro-2H-indol-2-oneHCID 3731012—
반응물5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic AcidHCID 11073792—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acidHCID 53395102101.4%

반응 조건

온도60 °C

반응 단계

The reaction mixture of 5-fluorooxindole (100 mg, 0.66 mmol), 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (133 mg, 0.79 mmol), and 10 drops of piperidine in ethanol (3 mL) was stirred at 60° C. overnight and filtered. The solid was washed with 1 M of aqueous hydrochloride solution, water, and dried to afford 5-(5-fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (201 mg, quantitative) as a yellow solid. MS m/z (relative intensity, %) 299 ([M−1]+., 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179910B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-5a1ac89513dd4fe09cb21b3a8bc68c56
출처 메모uspto-grants-2007_02