290326-06-6Relevant academic research and scientific papers
Method for preparing 1,4,7,10-tetraaza-2,6-pyridinophane
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, (2017/08/28)
The invention relates to a novel method for preparing 1,4,7,10-tetraaza-2,6-pyridinophane. 2,6-dimethylamino pyridine serving as a raw material is subjected to amino protection through o-/p-nitrobenzenesulfonyl and reacts with N,N-di(2-chloroethyl)-o-/p-n
Regioselective synthesis of N-functionalized 12-membered azapyridinomacrocycles bearing trialkylcarboxylic acid side chains
Siaugue, Jean-Michel,Segat-Dioury, Fabienne,Sylvestre, Isabelle,Favre-Réguillon, Alain,Foos, Jacques,Madic, Charles,Guy, Alain
, p. 4713 - 4718 (2007/10/03)
Selective protection of primary amine moieties of diethylenetriamine by 2-nitrophenylsulfonyl chloride followed by alkylation of the central N atom generates functionalized disulfonamide building blocks. When reacted with 2,6-bis(bromomethyl)pyridine following the Richman-Atkins methodology, such compounds yield the corresponding pyridine-containing azamacrocycles. Smooth removal of the N-sulfonyl groups provides versatile azamacrocyclic intermediates with transannular secondary amine functions. Subsequent N-alkylation regioselectively leads to tri N-functionalized 12-membered azapyridinomacrocycles bearing a sequence of N-acetate and N-propionate side chains.
A highly chemoselective protection and activation of primary amines in polyamine
Favre-Réguillon, Alain,Segat-Dioury, Fabienne,Nait-Bouda, Lalou,Cosma, Camlia,Siaugue, Jean-Michel,Foos, Jacques,Guy, Alain
, p. 868 - 870 (2007/10/03)
Functionalization of polyamines containing both primary and secondary amine moieties could be achieved with the use of 2-nitrobenzenesulfonyl chloride. In the presence of a secondary amine, the primary amine groups are selectively transformed into the cor
An efficient synthesis of pyridine containing triaza-macrocyclic triacetate ligand and luminescence properties of its europium(III) complex
Siaugue,Segat-Dioury,Favre-Reguillon,Madic,Foos,Guy
, p. 7443 - 7446 (2007/10/03)
Reaction of diethylenetriamine with 2-nitrobenzenesulfonyl chloride leads to an activated and protected compound that could be cyclized to N-protected aza-macrocycle. After a smooth deprotection step, the macrocycle was alkylated with chloroacetic acid le
