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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 440127Erstellt: 24. Oktober 2026

2-(6-(Bis(carboxymethyl)amino)-5-(2-(2-(bis(carboxymethyl)amino)-5-methylphenoxy)ethoxy)-2-benzofuranyl)-5-oxazolecarboxylic acid → Fura F

https://huagongshe.com/de/reaction/440127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(6-(Bis(carboxymethyl)amino)-5-(2-(2-(bis(carboxymethyl)amino)-5-methylphenoxy)ethoxy)-2-benzofuranyl)-5-oxazolecarboxylic acidHCID 57054—
EduktProton spongeHCID 88675—
EduktBaptaHCID 104751—
Edukt2,3-Difluoro-6-nitrophenolHCID 2733745—
EduktN,N'-[1,2-Ethanediylbis[oxy(4-fluoro-2,1-phenylene)]]bis[N-(carboxymethyl)glycine]HCID 11027644—
ProduktFura FHCID 3025888—

Reaktionsschritte

As discussed above, the synthesis of 5,5', 6,6'-tetrafluoro-BAPTA (Formula II) was carried out as originally described for both BAPTA and 5,5'-difluoro BAPTA starting from commercially available 2-nitro-5,6-difluorophenol. Fura-F was synthesized via the pathway originally described for the preparation of Fura-2. Unless otherwise noted commercially available reagents and dry solvents were used as received. Reactions were carried out under an atmosphere of argon and reaction temperatures refer to the bath. Flash column chromatography was performed with Merck Silica Gel 60 (40-63 μm). Proton sponge is 1,8-bis(dimethylamino)naphthalene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05516911
Quelldatensatzuspto-grants-1996_05
ORD IDord-76d2846edae443ab9eed0f43a815ffed
Quellennotizuspto-grants-1996_05