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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2197685생성일: 2026년 10월 23일

5-(3-(Trifluoromethyl)phenyl)furfural → 2-{4-Oxo-2-thioxo-5-[1-[5-(3-trifluoromethyl-phenyl)-furan-2-yl]-methylidene]-thiazolidin-3-ylamino}-benzoic acid

https://huagongshe.com/ko/reaction/2197685

반응식

참여 물질

역할이름HCID투입량
반응물5-(3-(Trifluoromethyl)phenyl)furfuralHCID 721837—
반응물HCID 4594337HCID 4594337—
반응물Ethylenediamine diacetateHCID 10154317—
반응물Sodium BisulfiteHCID 23665763—
용매MethanolHCID 887—
생성물2-{4-Oxo-2-thioxo-5-[1-[5-(3-trifluoromethyl-phenyl)-furan-2-yl]-methylidene]-thiazolidin-3-ylamino}-benzoic acidHCID 8664430279%

반응 단계

A mixture of 2-(4-oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acid (0.090 g, 0.34 mmol), 5-(3-trifluoromethyl-phenyl)-furan-2-carbaldehyde (0.086 g, 0.36 mmol) (purchased from Aldrich Chemical Company) and ethylenediamine diacetate (0.065 g, 0.036 mmol) in methanol (8 mL) was stirred at room temperature for 17 h. The reaction mixture was poured into stirred 0.6 N aq sodium hydrogensulfite (50 mL). The mixture was vigorously stirred for 15 mm. The solid product was filtered off and washed on funnel successively with 0.6 N aq sodium hydrogensulfite (2 mL), water (2×2 mL), ether (2 mL) and hexanes (2 mL). The material was dried in a vacuum oven at 65° C. for 19 h to afford 2-{4-Oxo-2-thioxo-5-[1-[5-(3-trifluoromethyl-phenyl)-furan-2-yl]-methylidene]-thiazolidin-3-ylamino}-benzoic acid (130 mg, 79%) as a solid. 1H NMR (400 MHz, DMSO-d6): δ 6.53 (1H, m), 6.86 (1H, m), 7.29 (1H, m), 7.43 (1H, d, J=3.6 Hz), 7.59 (1H, d, J=3.6 Hz), 7.78 (1H, s), 7.82 (2H, m), 7.92 (1H, m), 8.16 (1H, m), 8.21 (1H, m). LC/MS: APCI 489.3, HPLC 97.1%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338465B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-ba19cf6761d3480ab16ffcf3da0d1504
출처 메모uspto-grants-2012_12