The synthesis of the new C-nucleoside 6-deazaformycin B was written by Korouli, Stella;Lougiakis, Nikolaos;Marakos, Panagiotis;Pouli, Nicole. And the article was included in Synlett in 2008.Safety of 4-Methoxy-2-methylpyridine This article mentions the following:
The synthesis of the 6-deaza analog of formycin B I is described, through the condensation of lithiated 4-methoxy-2-methyl-3-trifluoroacetamidopyridine with a suitably protected ribonolactone, dehydration of the resulting hemiacetal, reduction and subsequent ring closure followed by protecting group manipulation. In the experiment, the researchers used many compounds, for example, 4-Methoxy-2-methylpyridine (cas: 24103-75-1Safety of 4-Methoxy-2-methylpyridine).
4-Methoxy-2-methylpyridine (cas: 24103-75-1) belongs to pyridine derivatives. Pyridine has a conjugated system of six π electrons that are delocalized over the ring. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. One of the examples of pyridines is the well-known alkaloid lithoprimidine, which is an A3 adenosine receptor antagonist and N,N-dimethylaminopyridine (DMAP) analog, commonly used in organic synthesis.Safety of 4-Methoxy-2-methylpyridine