1246815-83-7Relevant academic research and scientific papers
Synthetic method of pramipexole impurity B
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Paragraph 0042; 0046-0048, (2017/07/20)
The invention belongs to the technical field of medicine production and in particular to a preparation method of a pramipexole impurity. The synthetic method of the pramipexole impurity B comprises the following steps of: S1, adding (S)-2,6-diamino-4,5,6,7-tetrahydrobenzothiazole, alkali, propionic anhydride and DMAP into an organic solvent to synthesize (S)-N,N'-(4,5,6,7-tetrahydrobenzothiazole-2,6-diyl)dipropanamide; and S2, adding the (S)-N,N'-(4,5,6,7-tetrahydrobenzothiazole-2,6-diyl)dipropanamide obtained by the reaction in the S1 into an organic solvent and reducing system, wherein the reaction product is the pramipexole impurity B. The synthetic method of the pramipexole impurity B is simple in process route and convenient to operate, and the synthesized pramipexole impurity B can be used as a reference substance for detecting related substances of pramipexole, and the method is applied to quality control of pramipexole and related preparations.
B prumipexole hydrochloride method for synthesis of the material
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Paragraph 0014-0015; 0029; 0032-0033, (2017/02/09)
The invention provides a synthetic method of a pramipexole dihydrochloride related substance B shown by a formula I. The pramipexole dihydrochloride related substance B synthesized by the synthetic method is high in purity and can be directly used for quality control of related substances in pramipexole dihydrochloride; moreover, the synthetic method provided by the invention is simple and convenient in operation, readily-available in raw material, mild in reaction condition, good in repeatability, and suitable for production of the related substance B.
