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Although such salts must be pharmaceutically acceptable for administration to a subject, eg, a mammal, it is often desirable in practice to initially isolate a tetracycline compound of the invention from the reaction mixture as a pharmaceutically unacceptable salt and then simply convert the latter back to the free base compound by treatment with an alkaline reagent and subsequently convert the latter free base to a pharmaceutically acceptable acid addition salt!
I do not want to appear to advocate likelihood methods!
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