Synthetic Route of 96568-07-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.96568-07-9, Name is Ethyl 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate, molecular formula is C14H12ClFN2O3. In a article£¬once mentioned of 96568-07-9
It has been found that the Bu4NF/THF base/solvent couple is very efficient in the key cyclization step of (2) to (5) in the synthesis of antibacterial pyridonecarboxylic acid derivatives.In particular chiral intermediate (2d) is directly converted in one step to (4d), a key intermediate in the synthesis of (S)-Ofloxacin.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 96568-07-9
Reference£º
1,759-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N753 – PubChem