808-71-9Relevant articles and documents
Improved preparation method of penicillin hydriodate
-
Paragraph 0027; 0053-0064; 0067-0069; 0072-0073; 0076-0077, (2021/10/13)
The invention relates to the field of pharmacy, and particularly provides an improved preparation method of penicillin hydriodate, which comprises the following steps: 1) dissolving penicillin citrate with water, then adding a sodium iodide or potassium iodide solution for reaction, growing crystals, filtering, washing and drying to obtain the penicillin hydriodate. The method disclosed by the invention has the advantages of high yield, easiness in operation and small toxicity, the reaction condition is mild, the product purification, intermediate storage and impurity control are facilitated, and the penicillin hydriodate product with good stability is obtained.
Synthesis, isolation, and purification of benzylpenicillin β-diethylaminoethyl ester hydroiodide
Savel'Ev,Volkova,Kovalevskaya
scheme or table, p. 1230 - 1237 (2011/01/10)
Processes of synthesis, isolation, and purification of benzylpenicillin β-diethylaminoethyl ester hydroiodide were studied. The optimal conditions of benzylpenicillin esterification with chloroethyldiethylamine in dimetylformamide and acetonitrile were found. Processes for isolation of the target product were developed and its physicochemical properties were studied. Product stabilization conditions providing a stable pH value in solutions of benzylpenicillin β-diethylaminoethyl ester hydroiodide were found.