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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-(3-(Trifluoromethyl)phenyl)furfural | HCID 721837 | — |
| 반응물 | HCID 4594337 | HCID 4594337 | — |
| 반응물 | Ethylenediamine diacetate | HCID 10154317 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-{4-Oxo-2-thioxo-5-[1-[5-(3-trifluoromethyl-phenyl)-furan-2-yl]-methylidene]-thiazolidin-3-ylamino}-benzoic acid | HCID 86644302 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08338465B2 |
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| 출처 데이터셋 | uspto-grants-2012_12 |
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| ORD ID | ord-ba19cf6761d3480ab16ffcf3da0d1504 |
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| 출처 메모 | uspto-grants-2012_12 |
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