Synthesis method for moxifloxacin side chain
A moxifloxacin side chain and synthesis method technology, applied in the direction of organic chemistry, can solve the problems of many operation steps, environmental pollution, high cost, etc., and achieve the effect of reducing industrial waste, reducing production cost, and improving productivity
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[0022] The following is a clear and complete description of the technical solutions in the embodiments of the present invention. Apparently, the described embodiments are only some of the embodiments of the present invention, not all of them. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the protection scope of the present invention.
[0023] The embodiment of the present invention discloses a method for synthesizing moxifloxacin side chains with less industrial waste, low production cost and high productivity, using 2,3-pyridinedicarboxylic acid as raw material, through cyclization, catalytic hydrogenation, resolution, Racemization, chemical reduction, debenzylation to obtain moxifloxacin side chain, the specific synthesis method is:
[0024] S1, ring closure:
[0025] Add 120g of 2,3-pyridinedicarboxylic acid and 110g of acetic anhydride into the flask, stir...
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