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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2197680생성일: 2026년 10월 26일

2-(4-Oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acid → 2-{5-[1-[5-(5-tert-Butyl-2-hydroxy-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acid

https://huagongshe.com/reaction/2197680

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acidHCID 4594337—
반응물Ethylenediamine diacetateHCID 10154317—
반응물Sodium BisulfiteHCID 23665763—
반응물5-(5-Tert-butyl-2-hydroxy-phenyl)-furan-2-carbaldehydeHCID 59446233—
용매MethanolHCID 887—
생성물2-{5-[1-[5-(5-tert-Butyl-2-hydroxy-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acidHCID 8664429994%

반응 단계

A mixture of 2-(4-oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acid (0.078 g, 0.29 mmol), 5-(5-tert-butyl-2-hydroxy-phenyl)-furan-2-carbaldehyde and (0.075 g, 0.31 mmol) and ethylenediamine diacetate (0.056 g, 0.031 mmol) in methanol (10 mL) was stirred at room temperature for 18 h. The reaction mixture was poured into stirred 0.6 N aq sodium hydrogensulfite (50 mL). The mixture was vigorously stirred for 30 min. The solid product was filtered off and washed on funnel successively with 0.6 N aq sodium hydrogensulfite (1 mL), water (2×2 mL), ether (2×1 mL) and hexanes (2 mL). The material was dried in a vacuum oven at 65° C. for 17 h to afford 2-{5-[1-[5-(5-tert-Butyl-2-hydroxy-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acid (135 mg, 94%) as a solid. 1H NMR (400 MHz, DMSO-d6): δ 1.37 (9H, s), 6.98 (1H, d, J=8.4 Hz), 7.23 (1H, d, J=3.6 Hz), 7.34 (1H, dd, J=8.8, 2.8 Hz), 7.39 (1H, d, J=3.6 Hz), 7.70 (2H, m), 7.74 (1H, s), 7.94 (1H, d, J=2.4 Hz), 8.01 (1H, m), 8.07 (1H, m). LC/MS. APCI 493.1, HPLC 100%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338465B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-10ae44409558468b9c13a01ac7f714eb
출처 메모uspto-grants-2012_12