In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Convergent synthesis of 2-thioether-substituted (N)-methanocarba-adenosines as purine receptor agonists, published in 2021, which mentions a compound: 5451-40-1, mainly applied to thioether methanocarba adenosine purine receptor agonist convergent synthesis, Recommanded Product: 2,6-Dichloropurine.
A linear route has been used to prepare (N)-methanocarba-nucleoside derivatives, which serve as purine receptor ligands having a pre-established, receptor-preferred conformation. To introduce this rigid ribose substitute, a Mitsunobu reaction of a [3.1.0]bicyclohexane 5′-trityl intermediate 3 with a nucleobase is typically followed by functional group modifications. We herein report an efficient scalable convergent synthesis for 2-substituted (N)-methanocarba-adenosines, which were demonstrated to bind to the A3 adenosine receptor. The adenine moiety was pre-functionalized with 2-thioethers and other groups before coupling to the bicyclic precursor (3) as a key step to facilitate a high yield Mitsunobu product. This new approach provided the (N)-methanocarba-adenosines in moderate to good yield, which effectively increased the overall yield compared to a linear synthesis and conserved a key intermediate 3 (a product of nine sequential steps). The generality of this convergent synthesis, which is suitable as an optimized preclin. synthetic route, was demonstrated with various 2-thioether and 2-methoxy substituents.
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Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem