6533b862fe1ef96bd12c774f

RESEARCH PRODUCT

DOTAGA-anhydride: a valuable building block for the preparation of DOTA-like chelating agents.

Claire BernhardMathieu MoreauChristine GozeFranck DenatDamien LhenryFrançois BrunotteFrédéric BoschettiYoann Rousselin

subject

Magnetic Resonance SpectroscopyPropylamine[CHIM.THER]Chemical Sciences/Medicinal Chemistry010402 general chemistry01 natural sciencesCatalysisAnhydrideschemistry.chemical_compoundHeterocyclic Compounds 1-RingHeterocyclic CompoundsStructural isomerOrganic chemistryDOTAChelationReactivity (chemistry)BifunctionalChelating AgentsMolecular Structure010405 organic chemistryOrganic Chemistry[ CHIM.THER ] Chemical Sciences/Medicinal ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesAcetic anhydridechemistry

description

International audience; A DOTA derivative that contains an anhydride group was readily synthesized by reacting DOTAGA with acetic anhydride and its reactivity was investigated. Opening the anhydride with propylamine led to the selective formation of one of two possible regioisomers. The structure of the obtained isomer was unambiguously determined by 1D and 2D NMR experiments, including COSY, HMBC, and NOESY techniques. This bifunctional chelating agent offers a convenient and attractive approach for labeling biomolecules and, more generally, for the synthesis of a large range of DOTA derivatives. The scope of the reaction was extended to prepare DOTA-like compounds that contained various functional groups, such as isothiocyanate, thiol, ester, and amino acid moieties. This versatile building block was also used for the synthesis of a bimodal tag for SPECT or PET/optical imaging.

https://hal.archives-ouvertes.fr/hal-00932396