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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2197683Erstellt: 24. Oktober 2026

2-(4-Oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acid → 2-{5-[1-[5-(4-Tert-butyl-phenyl)-furan-2-yl]-meth-(e)-ylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acid

https://huagongshe.com/de/reaction/2197683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(4-Oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acidHCID 4594337—
EduktEthylenediamine diacetateHCID 10154317—
Edukt5-(4-Tert-butylphenyl)furan-2-carbaldehydeHCID 22566716—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelMethanolHCID 887—
Produkt2-{5-[1-[5-(4-Tert-butyl-phenyl)-furan-2-yl]-meth-(e)-ylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acidHCID 2477572587%

Reaktionsschritte

A mixture of 2-(4-oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acid (0.090 g, 0.34 mmol), 5-(4-tert-butyl-phenyl)-furan-2-carbaldehyde (0.082 g, 0.36 mmol) 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 min. 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-{5-[1-[5-(4-tert-Butyl-phenyl)-furan-2-yl]-meth-(E)-ylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acid (140 mg, 87%) as a solid. 1H NMR (400 MHz, DMSO-d6): δ 1.32 (9H, s), 6.45 (1H, m), 6.82 (1H, m), 7.23 (1H, m), 7.30 (1H, d, J=3.6), 7.40 (1H, d, J=3.6), 7.61 (2H, m), 7.74 (1H, s), 7.82 (2H, m), 7.91 (1H, m), 11.20 (1H, bs). LC/MS APCI 477.9, HPLC 91.0%

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08338465B2
Quelldatensatzuspto-grants-2012_12
ORD IDord-0666dfb1d4304484be56ae3659c14898
Quellennotizuspto-grants-2012_12