Final Thoughts on Chemistry for 2-Amino-9-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3H-purine-6,8(7H,9H)-dione

Synthetic Route of 88847-89-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 88847-89-6.

Some examples of the diverse research done by chemistry experts include discovery of new medicines and vaccines, improving understanding of environmental issues, and development of new chemical products and materials. 88847-89-6, Name is 2-Amino-9-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3H-purine-6,8(7H,9H)-dione, molecular formula is C10H13N5O5, Synthetic Route of 88847-89-6, belongs to naphthyridine compound, is a common compound. In a patnet, author is Bhambi, Dinesh, once mentioned the new application about 88847-89-6.

5-(4-Substitutedphenyl)-8,8-dimethyl-5,8,9,10-tetrahydrobenzo[b][1,8]naphthyridin-7H-one 1a-e have been converted to their N-substituted alkoxyphthalamide derivatives using two alternative pathways. In route one, 1a-e are treated with formalin (37%) to yield 5-(4-substitutedphenyl)-10-(hydroxymethyl)-8,8-dimethyl-5,8,9,10-tetrahydrobenzo[b][1,8]naphthyriding-6-7H-one 2a-e, which is further changed to corresponding chloro derivatives 3a-e by the treatment with thionyl chloride. Condensation of 3a-e with N-hydroxyphthalimide furnished the final compounds 2-{[5-(4-substitutedphenyl)-8,8-dimethyl-6-oxo-6,7,8,9-tetrahydrobenzo[b][1,8]naphthyridin-10-5H-yl]mehtoxy}phthalimide 4a-e. In another route, 1a-e is directly condensed with omega-bromoalkoxyphthalimide to yield Higher homologues of 4a-e i.e. 2-{2-[5-(4-substituted phenyl)-8,8-dimethyl-6-oxo-6,7,8,9-tetrahydrobenzo[b][1,8]naphthyriding-10-5H-yl]ehtody} phthalimide derivatives 5a-e. Structures of all the synthesized compounds have been established on the basis of elemental analysis and spectral studies. All the synthesized compounds have been screened for antibacterial and antifungal activities.

Synthetic Route of 88847-89-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 88847-89-6.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem