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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 377012Erstellt: 24. Oktober 2026

Borane;pyridine → p-NO2-Bn-Cyclen

https://huagongshe.com/de/reaction/377012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBorane;pyridineHCID 2723995—
Edukt2-(4-Nitrobenzyl)-3,6,9,12-tetraoxo-1,4,7,10-tetraazacyclododecaneHCID 19360715—
LösungsmittelPyridineHCID 1049—
Produktp-NO2-Bn-CyclenHCID 10892179—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Borane-pyridine (available from Aldrich) is added to a suspension of 2-(4-nitrobenzyl)-3,6,9,12-tetraoxo-1,4,7,10-tetraazacyclododecane in pyridine. The mixture is heated under reflux at 120° C. for 14 hours. The solvent is removed under reduced pressure. The residue is taken up in methanol and heated under reflux for 2 hours. The solvent is removed under reduced pressure. The residue is dissolved in methanol and re-evaporated. The solid residue is purified by chromatography on reverse phase Baker G18 silica gel available from J.T. Baker, Inc., Phillipsburg, N.J. Conversion of this product to nitro-benzyl-DOTA is accomplished via the procedure discussed in Renn et al., Bioconj. Chem., 3:563-569, 1992 or as set forth is subpart A above.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06022966
Quelldatensatzuspto-grants-2000_02
ORD IDord-c56b42dd4f524a2cb77c8c68b9f4c7bc
Quellennotizuspto-grants-2000_02