Productive process for Rufloxaxin Hydrochloride raw material

A rufloxacin hydrochloride and production process technology, which is applied in the field of improved production process of rufloxacin hydrochloride crude drug, can solve problems such as unrecoverable fluoboric acid, high production cost, difficult equipment selection, etc., and achieve product yield High, short production cycle, the effect of cost reduction

Inactive Publication Date: 2002-07-17
WUHAN BINHU DOUBLE CRANE PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] In this process route, 40% fluoboric acid is a very corrosive strong acid at a high temperature of 100-120 ° C. It can corrode enamel, stainless steel, polyphenylene sulfide, glass, etc., which causes great difficulties in equipment selection. , causing expensive production costs, corroding the reaction vessel, consuming a large amount of fluoboric acid, and producing by-products, which reduces the yield. In the post-processing process, because fluoboric acid cannot be recovered, certain pollution is generated

Method used

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Embodiment Construction

[0032]As mentioned above, the present invention is an improvement to the original process, so most of the content in the process is the prior art, only the second step and the sixth step process are simplified, and its specific implementation can be carried out according to the above-mentioned technical scheme. . A, 2-mercaptoethanol, dehydrated alcohol, triethylamine and water can be taken as 184.5KG, 82.2KG, 500L, 102KG, 200L in the above-mentioned first-step process respectively; the six kinds of materials added in the above-mentioned second-step process Can take ethanol 300L, water 200L, ammonium chloride 5.3KG, iron powder 200KG, dilute hydrochloric acid 60L and nitro compound B273KG respectively; In the above-mentioned 3rd step process, C, hydrobromic acid can be taken respectively as 205KG, 656L; In the step process, D, ethanol, and water can be respectively taken as 430KG, 500L, and 500L; in the above-mentioned 5th step process, E, EMME, polyphosphoric acid, and water ...

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PUM

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Abstract

The production process of raw material medicine of rufluoxin hydrochloride is an improvement on oil technological process, and is aimed at overcome defects of old technological process whose production yield is low, cost is high and by-product can pollute environment. It mainly improves second step and sixth step of old technological process, in second step, in the reaction container the ethyl alcohol, water ammonium chloride are added, iron powder is added while stirring, the dilute hydrochloric acid is slowly added, heated to reflux state, B is dropped in slowly, pH value is retained to 5-6, reacted for 1 hr, then TLC is ued to test reaction end point; and in sixth step, in reaction container the F, boron trifluoride etherate and acetone are added, heated to 58-63 deg.C and reflux reaction is made for 3-3.5 hr. Said invention can reduce production cost and raise product yield.

Description

technical field [0001] The invention relates to a production process of medicines, in particular to an improved production process of rufloxacin hydrochloride crude drug. Background technique [0002] The production process of rufloxacin API was limited to laboratory experiments at that time, and there were few considerations in the selection of certain raw materials, the capacity of production equipment, and the operating conditions of certain steps, which led to many problems in production, such as: production receipts. The rate is lower, the cost is higher, and the environment is polluted. In particular, there are many problems in the second and sixth steps. [0003] In the production process route of the former second step amide C, in the reaction vessel equipped with a stirrer, a thermometer, a dropping funnel and an addition funnel, add nitro compound A, ethanol, water, and ammonium chloride; be warming up to 40 ° C ; Add hydrochloric acid dropwise...

Claims

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Application Information

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IPC IPC(8): C07C319/12C07C323/19C07C323/34C07D279/16C07D513/04
Inventor 彭自强
Owner WUHAN BINHU DOUBLE CRANE PHARMA
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