Method for reducing residual quantity of dichloromethane in ampicillin

A technology of ampicillin and dichloromethane, which is applied in the field of reducing the residual amount of dichloromethane in ampicillin, can solve the problems of affecting economic benefits, the decline of amoxicillin yield, and the inability to balance quality and yield, and achieve a large yield , the effect of high purity

Active Publication Date: 2015-10-07
NORTH CHINA PHARM GRP SEMISYNTECH CO LTD
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0003] So far, there are few relevant reports about reducing methylene chloride residues in ampicillin and amoxicillin products, and the method selected cannot take into account both quality and yield, such as "reducing methylene chloride residues in amoxicillin experiment" ( Qi Weidong, "Heilongjiang Science and Technology Information Worker", No. 18, June 2010, page 14) reduces the residual dichloromethane in amoxicillin by increasing the amount of water, but it will reduce the yield of amoxicillin by 1.0 %~1.5%, which affects economic benefits, and it is mentioned in the literature that amoxicillin is unstable in case of acid, alkali and heat, and the yield of amoxicillin will decrease when the extraction temperature taken is 20~23°C

Method used

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  • Method for reducing residual quantity of dichloromethane in ampicillin
  • Method for reducing residual quantity of dichloromethane in ampicillin
  • Method for reducing residual quantity of dichloromethane in ampicillin

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Effect test

Embodiment 1

[0038]Add 100mL of the primary aqueous phase obtained in the hydrolysis process in the chemical synthesis of ampicillin into the reactor; according to the volume ratio of the solvent and the primary aqueous phase being 1.0, add 100mL of n-hexane to extract the primary aqueous phase of ampicillin. At this time, the primary aqueous phase of ampicillin is The residual dichloromethane in the phase is 15000ppm; the mixed solution is stirred rapidly at 13°C for 20min, and after standing for 10min, the phases are separated to obtain a secondary aqueous phase and a secondary organic phase. The secondary aqueous phase is mainly ampicillin. At this time The residual dichloromethane in the secondary water phase is 550ppm; therefore, when the volume ratio of n-hexane to the primary water phase is 1.0, the removal rate of dichloromethane is 95.51% when n-hexane is applied mechanically once. The secondary organic phase is mainly n-hexane; the secondary aqueous phase containing ampicillin is ...

Embodiment 2

[0041] Add 100mL of the primary water phase obtained in the hydrolysis process in the chemical synthesis of ampicillin into the reactor; according to the volume ratio of the solvent and the primary water phase of 0.4, add 40mL of n-heptane to extract the primary water phase of ampicillin, and at this time, the primary water phase of ampicillin is The dichloromethane residue in the water phase was 16000ppm; the mixed solution was stirred rapidly at 15°C for 10 minutes, and after standing for 10 minutes, the phases were separated to obtain a secondary water phase and a secondary organic phase. The secondary water phase was mainly ampicillin. When the dichloromethane residue in the secondary water phase is 350ppm; therefore when the volume ratio of n-heptane to the primary water phase is 0.4, the removal rate of dichloromethane when n-heptane is applied mechanically once is 97.8%. The secondary organic phase is mainly n-heptane; the secondary aqueous phase containing ampicillin is...

Embodiment 3

[0044] Add 100mL of the primary aqueous phase obtained in the hydrolysis process in the chemical synthesis of ampicillin into the reactor; according to the volume ratio of the solvent and the primary aqueous phase of 0.6, add 60mL of ethyl acetate to extract the primary aqueous phase of ampicillin, and at this time, the primary aqueous phase of ampicillin is The residual dichloromethane in the water phase was 15000ppm; the mixed solution was stirred rapidly at 10°C for 20 minutes, and after standing for 15 minutes, the phases were separated to obtain a secondary water phase and a secondary organic phase. The secondary water phase was mainly ampicillin. The residual dichloromethane in the secondary water phase is 400ppm, so when the volume ratio of ethyl acetate to the primary water phase is 0.5, the removal rate of dichloromethane is 97.3% when ethyl acetate is applied mechanically once. The secondary organic phase is mainly ethyl acetate; the secondary aqueous phase containing...

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Abstract

The invention discloses a method for reducing the residual quantity of dichloromethane in ampicillin. The method comprises the following steps: 1, adding a primary water phase obtained in a hydrolysis process for chemical synthesis of ampicillin into a reactor; 2, adding a solvent to the ampicillin water phase in order to carry out extraction; 3, rapidly stirring, standing, and separating to obtain a secondary water phase and a secondary organic phase; 4, crystallizing the secondary water phase, growing obtained crystals, washing and drying to obtain finished ampicillin; and 5, carrying out treatment processes in step 2 and step 3 on the secondary organic phase. A solvent extraction technology is adopted to reduce the residual quantity of dichloromethane in ampicillin, so the finished ampicillin has large yield and high purity.

Description

technical field [0001] The invention relates to a method for reducing drug solvent residues, in particular to a method for reducing methylene chloride residues in ampicillin. Background technique [0002] Ampicillin is white or off-white powder or crystal, odorless, slightly bitter taste, easily soluble in water, slightly soluble in ethanol, insoluble in ether. Ampicillin is a β-lactam antibiotic used to treat respiratory tract infections, gastrointestinal tract infections, and endocarditis caused by sensitive bacteria. At present, when industrial production uses chemical methods to synthesize ampicillin, dichloromethane needs to be used as a solvent in the reaction process. Due to the special requirements of the pharmaceutical industry, in order to ensure the effectiveness and safety of drugs for patients, the United States, the European Union, Japan and my country It is stipulated that for ampicillin, the residual amount of dichloromethane is not allowed to exceed 600ppm. ...

Claims

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Application Information

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Patent Type & AuthorityApplications(China)
IPC IPC(8): C07D499/18C07D499/68
CPCC07D499/18C07D499/68
Inventor左丽华严正人魏士倩朱军刘慧勤周宏宇
OwnerNORTH CHINA PHARM GRP SEMISYNTECH CO LTD