CN1765902A - One-step preparation process of aseptic ceftriaxone sodium for injection - Google Patents
One-step preparation process of aseptic ceftriaxone sodium for injection Download PDFInfo
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- CN1765902A CN1765902A CN 200510118236 CN200510118236A CN1765902A CN 1765902 A CN1765902 A CN 1765902A CN 200510118236 CN200510118236 CN 200510118236 CN 200510118236 A CN200510118236 A CN 200510118236A CN 1765902 A CN1765902 A CN 1765902A
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- Prior art keywords
- ceftriaxone sodium
- aseptic
- solvent
- sodium
- preparation process
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- 229960000479 ceftriaxone sodium Drugs 0.000 title claims abstract description 38
- FDRNWTJTHBSPMW-GNXCPKRQSA-L disodium;(6r,7r)-7-[[(2e)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(2-methyl-6-oxido-5-oxo-1,2,4-triazin-3-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound [Na+].[Na+].S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)/C(=N/OC)C=2N=C(N)SC=2)CC=1CSC1=NC(=O)C([O-])=NN1C FDRNWTJTHBSPMW-GNXCPKRQSA-L 0.000 title claims abstract description 38
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 238000002347 injection Methods 0.000 title claims abstract description 17
- 239000007924 injection Substances 0.000 title claims abstract description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 42
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims abstract description 33
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 28
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000002904 solvent Substances 0.000 claims abstract description 22
- 238000003756 stirring Methods 0.000 claims abstract description 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000002425 crystallisation Methods 0.000 claims abstract description 18
- 230000008025 crystallization Effects 0.000 claims abstract description 18
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 150000002148 esters Chemical class 0.000 claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 239000013078 crystal Substances 0.000 claims abstract description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000001335 aliphatic alkanes Chemical class 0.000 claims abstract description 7
- 150000001412 amines Chemical class 0.000 claims abstract description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 43
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 239000012046 mixed solvent Substances 0.000 claims description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 claims description 12
- 229960004756 ethanol Drugs 0.000 claims description 12
- 239000003960 organic solvent Substances 0.000 claims description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 11
- 238000005352 clarification Methods 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 9
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- 230000001476 alcoholic effect Effects 0.000 claims description 6
- 150000005826 halohydrocarbons Chemical class 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 claims description 5
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 5
- 239000001632 sodium acetate Substances 0.000 claims description 5
- 235000017281 sodium acetate Nutrition 0.000 claims description 5
- 229940043279 diisopropylamine Drugs 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 claims description 3
- 229960000935 dehydrated alcohol Drugs 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims description 2
- 239000012433 hydrogen halide Substances 0.000 claims description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 238000000247 postprecipitation Methods 0.000 claims description 2
- 238000011146 sterile filtration Methods 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 10
- 238000001035 drying Methods 0.000 abstract description 7
- 238000001914 filtration Methods 0.000 abstract description 6
- 159000000000 sodium salts Chemical class 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 4
- AZZMGZXNTDTSME-JUZDKLSSSA-M cefotaxime sodium Chemical compound [Na+].N([C@@H]1C(N2C(=C(COC(C)=O)CS[C@@H]21)C([O-])=O)=O)C(=O)\C(=N/OC)C1=CSC(N)=N1 AZZMGZXNTDTSME-JUZDKLSSSA-M 0.000 abstract 1
- 229960002727 cefotaxime sodium Drugs 0.000 abstract 1
- 239000007810 chemical reaction solvent Substances 0.000 abstract 1
- 238000004140 cleaning Methods 0.000 abstract 1
- 230000007423 decrease Effects 0.000 abstract 1
- 235000019439 ethyl acetate Nutrition 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 238000005516 engineering process Methods 0.000 description 10
- 239000004278 EU approved seasoning Substances 0.000 description 5
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000012065 filter cake Substances 0.000 description 5
- 235000011194 food seasoning agent Nutrition 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 5
- 238000000967 suction filtration Methods 0.000 description 5
- 229960004249 sodium acetate Drugs 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 206010056519 Abdominal infection Diseases 0.000 description 1
- 206010051548 Burn infection Diseases 0.000 description 1
- 229930186147 Cephalosporin Natural products 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- 206010018612 Gonorrhoea Diseases 0.000 description 1
- 201000009906 Meningitis Diseases 0.000 description 1
- 206010067268 Post procedural infection Diseases 0.000 description 1
- 206010037596 Pyelonephritis Diseases 0.000 description 1
- 206010057190 Respiratory tract infections Diseases 0.000 description 1
- 206010040047 Sepsis Diseases 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- -1 Sodium isooctanoates Chemical class 0.000 description 1
- 206010062255 Soft tissue infection Diseases 0.000 description 1
- 206010048038 Wound infection Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000000013 bile duct Anatomy 0.000 description 1
- 229940124587 cephalosporin Drugs 0.000 description 1
- 150000001780 cephalosporins Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 206010034674 peritonitis Diseases 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000000384 rearing effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 208000013223 septicemia Diseases 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 206010040872 skin infection Diseases 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 210000004872 soft tissue Anatomy 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
Abstract
The invention relates to an improved preparation technique for Ceftriaxone Sodium, which comprises: with nitrogen protection, in solvent, reacting between 7-ACT and AE-active ester with amine as intermediate; adding benzothiazole as assisting solvent and sodium salt agent, separating and crystallizing to obtain the product. Wherein, the reaction solvent comprises halogenated hydrocarbon of alkane, acetic ester or acetone and alcohol and water; stirring the 7-ACT and AE-active ester till clear, adding assisting solvent of benzothiazole and salt agent; extracting, degerming, filtering, adding insoluble solvent for Ceftriaxone Sodium; when liquid shows turbid, feeding crystal; separating the crystal by insoluble solvent to cefotaxime sodium; cleaning, drying treatment to obtain the product for injection. This invention needs just one-step operation, has good crystallization and short production period, improves product yield, and decreases solvent harm to operation crews.
Description
Technical field
The present invention relates to a kind of preparation technology of improved ceftriaxone sodium, belong to the preparing technical field of compound.
Background technology
Ceftriaxone sodium is a third generation broad-spectrum cephalosporin, be widely used in to this product sensitivity respiratory tract infection, urinary system infection, comprise pyelonephritis and gonorrhoea, septicemia, meningitis, burn infection, postoperative infection, osteoarthrosis, soft tissue, skin and wound infection, abdominal infection (peritonitis, bile duct and intestines and stomach infect) etc. and average of operation periods infection mitigation.Existing ceftriaxone sodium preparation technology operates in two steps; by nitrogen protection; in the single solvent of methylene dichloride; react under the effect of triethylamine intermediate reaction thing by 7-ACT and AE-active ester, add the benzothiazole solubility promoter, add salt forming agent again; the acquisition crystallization is a coarse salt of ceftriaxone sodium; in that crude salt is water-soluble, after handling through degerming, decolouring again, crystallisate is separated out with acetone.The operation of two step process, the solvent usage quantity is big, and is seriously polluted, and labour intensity is big, and the production cycle is long, and the production cost height is at the bottom of the product yield.
Summary of the invention
The object of the present invention is to provide a kind of one-step preparation process of aseptic ceftriaxone sodium for injection, the solvent usage quantity is few, and labour intensity is little, and is with short production cycle, and production cost is low, the product yield height.
The one-step preparation process of aseptic ceftriaxone sodium for injection of the present invention; by nitrogen protection; in solvent; react under the effect of amine intermediate reaction thing by 7-ACT and AE-active ester; add the benzothiazole solubility promoter; adding salt forming agent again reacts and separates out crystallization and make; its mixed solvent is the halohydrocarbon by alkane; the mixed solvent that ethyl acetate or acetone and alcoholic solvent and water are formed; extremely clarification of stirring reaction in 7-ACT and AE-active ester; add the benzothiazole solubility promoter, add salt forming agent again, extracting and demixing; Sterile Filtration; the insoluble organic solvent that adds ceftriaxone sodium again when treating that solution becomes is muddy, carries out growing the grain and handles; the insoluble organic solvent that adds ceftriaxone sodium is then separated out crystallization, passes through conventional crystallizing and washing at last; dry aftertreatment gets the aseptic ceftriaxone sodium for injection finished product.
Reaction equation is: (videing infra)
Technology of the present invention can not need to make in advance crude salt owing to adopted mixed solvent, directly accomplishes the ceftriaxone sodium aseptic powder from 7-ACT.And the solvent usage quantity reduces significantly, only be 50% of original technology, easy to operate, be easy to control, (shortening 4 hours more originally) with short production cycle, labour intensity is little, production cost is low, can also improve product yield 5%, and yield reaches 93%, the solvent consumption is few, has also reduced the harm of solvent to operator.
Among the present invention:
The composition volume ratio of mixed solvent is:
The halohydrocarbon of alkane, ethyl acetate or acetone: alcoholic solvent: water=10: (1～5): (0～2).
The halohydrocarbon of alkane can be a kind of in methylene dichloride, the chloroform etc.
Alcoholic solvent can be in ethanol, methyl alcohol or the Virahol etc. a kind of.
The benzothiazole solubility promoter is a kind of in organic acid, two (trichloromethyl) carbonic ether, chlorocarbonic acid dimethyl ester, hydrogen halide or other halogenide.
Amine intermediate reaction thing can be in triethylamine, Diisopropylamine or the tertiary amine a kind of.
Salt forming agent is a kind of in organic sodium salts such as sodium bicarbonate, Sodium isooctanoate, sodium acetate (sodium-acetate), sodium methylate, yellow soda ash and the inorganic sodium, can be sodium salt solution, also can be solid sodium salt, and sodium salt solution is dissolved in the mixed solvent by sodium salt to be made.
Extremely clarification of stirring reaction in 7-ACT and AE-active ester preferably adds organic acid or mineral acid solubility promoter and produces post precipitation, carries out salify, extraction, layering processing again.
The insoluble organic solvent of ceftriaxone sodium has one or more the mixing in methylene dichloride, acetone, ethyl acetate, dehydrated alcohol or the Virahol.
Add when salt-forming reaction question response solution becomes is muddy behind the salt forming agent, can add the ceftriaxone sodium powder and do crystal seed and carry out growing the grain again and handle, can improve crystalline condition, improve crystalline quality.
The production of product will meet industry requirement, and the same routine operation of other process condition of not mentioning in detail, batching situation as reactant meets the reactional equation requirement, amine intermediate reaction thing and 7-ACT consumption proportion relation, the adding situation of benzothiazole solubility promoter and salt forming agent (solubility promoter and salt forming agent add-on are 7-ACT charging capacity 0.5～2%), 5～10 ℃ of temperature of reaction, rearing crystal time 0.5～1 hour, crystallization time 1～5 hour, crystalline washing requirement, 40～50 ℃ of drying temperatures, vacuum drying vacuum degree control is 0.095～0.099MPa, or the like.
Process using of the present invention mixed solvent, realized directly accomplishing the ceftriaxone sodium aseptic powder from 7-ACT without the direct salify of crude salt, the solvent usage quantity is few, labour intensity is little, and is with short production cycle, and production cost is low, the product yield height, quality is good, and solvent is little to operator's harm, is beneficial to industrial practicing.
Embodiment
The invention will be further described below in conjunction with embodiment.
Embodiment 1
The preparation technology of ceftriaxone sodium of the present invention is as follows:
50ml methylene dichloride, 20ml ethanol, 18ml triethylamine, 5ml water are added in the three-necked bottle, under nitrogen protection, stir cooling; 5 ℃ of temperature add 20g7-ACT, 20gAE-active ester, 0.5g sodium bisulfite oxidation inhibitor; Stirring reaction, 6 ℃ of temperature; The reaction clarification, adding aqueous hydrochloric acid accent PH is 3.5, stirs 30 minutes, adds Sodium isooctanoate 10 grams, layering, filtration; Drip the insoluble organic solvent of acetone; Solution is little muddy, adds the crystal seed growing the grain; Drip the acetone crystallization, 10 ℃ of temperature; Suction filtration gets the crystallization filter cake, uses washing with acetone; 50 ℃ of hot-air seasonings; Drying finish product.
Receive dry product 33.03g, yield 92.78% (in 7-ACT).
Embodiment 2
The preparation technology of ceftriaxone sodium of the present invention is as follows:
50ml methylene dichloride, 20ml ethanol, 18ml triethylamine, 5ml water are added in the three-necked bottle, under nitrogen protection, stir cooling; 5 ℃ of temperature add 20g7-ACT, 20gAE-active ester, 0.5g sodium bisulfite oxidation inhibitor; Stirring reaction, 7 ℃ of temperature; The reaction clarification, adding aqueous acetic acid accent PH is 4, stirs 25 minutes, adds sodium acetate 10 grams, layering, filtration; Drip the insoluble organic solvent of acetone; Solution is little muddy, adds the crystal seed growing the grain; Drip the acetone crystallization, 10 ℃ of temperature; Suction filtration gets the crystallization filter cake, uses washing with acetone; 50 ℃ of hot-air seasonings; Drying finish product.
Receive dry product 33.01g, yield 92.67% (in 7-ACT).
Embodiment 3
The preparation technology of ceftriaxone sodium of the present invention is as follows:
50ml methylene dichloride, 25ml ethanol, 18ml triethylamine, 5ml water are added in the three-necked bottle, under nitrogen protection, stir cooling; 8 ℃ of temperature add 20g7-ACT, 20gAE-active ester, 0.5g sodium bisulfite oxidation inhibitor; Stirring reaction, 8 ℃ of temperature; The reaction clarification, adding aqueous hydrochloric acid accent PH is 3, stirs 35 minutes, adds Sodium isooctanoate 10 grams, layering, filtration; Drip the insoluble organic solvent of Virahol; Solution is little muddy, adds the crystal seed growing the grain; Drip the Virahol crystallization, 8 ℃ of temperature; Suction filtration gets the crystallization filter cake, uses washed with isopropyl alcohol; 50 ℃ of hot-air seasonings; Drying finish product.
Embodiment 4
The preparation technology of ceftriaxone sodium of the present invention is as follows:
50ml methylene dichloride, 20ml ethanol, 18ml Diisopropylamine are added in the three-necked bottle, under nitrogen protection, stir cooling; 7 ℃ of temperature add 20g7-ACT, 20gAE-active ester, 0.5g sodium bisulfite oxidation inhibitor; Stirring reaction, 8 ℃ of temperature; The reaction clarification, adding aqueous hydrochloric acid accent PH is 4.5, stirs 28 minutes, adds sodium acetate 11 grams, layering, filtration; The insoluble organic solvent of drip dichloromethane; Solution is little muddy, drip dichloromethane crystallization, 10 ℃ of temperature; Suction filtration gets the crystallization filter cake, uses washed with dichloromethane; 50 ℃ of hot-air seasonings; Drying finish product.
Embodiment 5
The preparation technology of ceftriaxone sodium of the present invention is as follows:
50ml methylene dichloride, 20ml ethanol, 18ml triethylamine, 10ml water are added in the three-necked bottle, under nitrogen protection, stir cooling; 9 ℃ of temperature add 20g7-ACT, 20gAE-active ester, 0.5g sodium bisulfite oxidation inhibitor; Stirring reaction, 9 ℃ of temperature; The reaction clarification, adding aqueous hydrochloric acid accent PH is 3.5, stirs 30 minutes, adds Sodium isooctanoate (13 gram Sodium isooctanoates dissolve in the 30ml mixed solvent and make), layering, filtration; Drip the insoluble organic solvent of acetone; Solution is little muddy, adds the crystal seed growing the grain; Drip the acetone crystallization, 10 ℃ of temperature; Suction filtration gets the crystallization filter cake, uses washing with acetone; 50 ℃ of hot-air seasonings; Drying finish product.
Embodiment 6～10
Methylene dichloride in the mixed solvent is replaced by ethyl acetate, and other situation is respectively with embodiment 1～5.
Embodiment 11～15
Methylene dichloride in the mixed solvent is replaced by acetone, and other situation is respectively with embodiment 1～5.
Embodiment 16～20
Ethanol in the mixed solvent is replaced by methyl alcohol, and other situation is respectively with embodiment 1～5.
Embodiment 21～25
Ethanol in the mixed solvent is replaced by Virahol, and other situation is respectively with embodiment 1～5.
Embodiment 26～30
Methylene dichloride in the mixed solvent is replaced by ethyl acetate, and ethanol is replaced by methyl alcohol, and other situation is respectively with embodiment 1～5.
Embodiment 31～35
Methylene dichloride in the mixed solvent is replaced by acetone, and ethanol is changed to methyl alcohol, and other situation is respectively with embodiment 1～5.
Embodiment 36～40
Methylene dichloride in the mixed solvent is replaced by ethyl acetate, and ethanol is changed to Virahol, and other situation is respectively with embodiment 1～5.
Embodiment 41～80
With the benzothiazole solubility promoter---hydrochloric acid is replaced by the chlorocarbonic acid dimethyl ester, and other situation is respectively with embodiment 1～40.
Embodiment 81～120
With the benzothiazole solubility promoter---hydrochloric acid is replaced by hydrogen iodide, other situation is respectively with embodiment 1～40.
Embodiment 121～240
Amine intermediate reaction thing triethylamine is replaced by Diisopropylamine, and other situation is respectively with embodiment 1～120.
The mixed solution that the insoluble organic solvent that is used for the ceftriaxone sodium of crystallization in the foregoing description is replaced with mixed solution, methylene dichloride and the ethyl acetate arbitrary proportion of dehydrated alcohol, Virahol or methylene dichloride and acetone arbitrary proportion is respectively tested, and the test situation proof all can.
Claims (10)
1; a kind of one-step preparation process of aseptic ceftriaxone sodium for injection; by nitrogen protection; in solvent; react under the effect of amine intermediate reaction thing by 7-ACT and AE-active ester; add the benzothiazole solubility promoter; adding salt forming agent again reacts and separates out crystallization and make; it is characterized in that mixed solvent is the halohydrocarbon by alkane; the mixed solvent that ethyl acetate or acetone and alcoholic solvent and water are formed; extremely clarification of stirring reaction in 7-ACT and AE-active ester; add the benzothiazole solubility promoter, add salt forming agent again, extracting and demixing; Sterile Filtration; the insoluble organic solvent that adds ceftriaxone sodium again when treating that solution becomes is muddy, carries out growing the grain and handles; the insoluble organic solvent that adds ceftriaxone sodium is then separated out crystallization, passes through conventional crystallizing and washing at last; dry aftertreatment gets the aseptic ceftriaxone sodium for injection finished product.
2, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 is characterized in that the composition volume ratio of mixed solvent is: the halohydrocarbon of alkane, ethyl acetate or acetone: alcoholic solvent: water=10: (1～5): (0～2).
3, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 and 2, the halohydrocarbon that it is characterized in that alkane is a methylene dichloride.
4, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 and 2 is characterized in that alcoholic solvent is ethanol or methyl alcohol.
5, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 is characterized in that the benzothiazole solubility promoter is a kind of in chlorocarbonic acid dimethyl ester, hydrogen halide or other halogenide.
6, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 is characterized in that amine intermediate reaction thing is triethylamine or Diisopropylamine.
7, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1, it is characterized in that extremely clarification of stirring reaction in 7-ACT and AE-active ester, add organic acid or mineral acid benzothiazole solubility promoter and produce post precipitation, carry out salify, extraction, layering processing again.
8, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 is characterized in that salt forming agent is Sodium isooctanoate or sodium acetate.
9, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 8, the insoluble organic solvent that it is characterized in that ceftriaxone sodium are one or more the mixing in methylene dichloride, acetone, ethyl acetate, dehydrated alcohol or the Virahol.
10, the one-step preparation process of aseptic ceftriaxone sodium for injection according to claim 1 is characterized in that adding when solution becomes is muddy behind the salt forming agent, adds the ceftriaxone sodium powder and does crystal seed and carry out growing the grain again and handle.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005101182366A CN100335485C (en) | 2004-10-27 | 2005-10-21 | One-step preparation process of aseptic ceftriaxone sodium for injection |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN200410155401.0 | 2004-10-27 | ||
| CN 200410155401 CN1634933A (en) | 2004-10-27 | 2004-10-27 | Process for preparing ceftriaxone sodium |
| CNB2005101182366A CN100335485C (en) | 2004-10-27 | 2005-10-21 | One-step preparation process of aseptic ceftriaxone sodium for injection |
Publications (2)
| Publication Number | Publication Date |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011012965A1 (en) * | 2009-07-27 | 2011-02-03 | Nectar Lifesciences Ltd. | Improved process for preparation of ceftriaxone disodium hemiheptahydrate |
| CN104031067A (en) * | 2014-05-21 | 2014-09-10 | 丽珠医药集团股份有限公司 | Refinement method of ceftriaxone sodium crude product |
| CN104876948A (en) * | 2015-05-28 | 2015-09-02 | 华北制药河北华民药业有限责任公司 | Preparation method of ceftriaxone sodium |
| CN106008554A (en) * | 2016-05-23 | 2016-10-12 | 河南康达制药有限公司 | Preparation method and product of ceftriaxone sodium sterile powder |
| CN106366099A (en) * | 2016-08-22 | 2017-02-01 | 山东罗欣药业集团恒欣药业有限公司 | Anti-infection medicine ceftriaxone sodium crystal compound and preparation method thereof |
| CN110396101A (en) * | 2018-12-03 | 2019-11-01 | 广东金城金素制药有限公司 | Qu Suofen Ceftriaxone Sodium pharmaceutical preparation treats the new indication of bacillary intimitis |
| CN112679524A (en) * | 2020-12-24 | 2021-04-20 | 华北制药河北华民药业有限责任公司 | Preparation method of ceftriaxone sodium |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102875574A (en) * | 2012-08-31 | 2013-01-16 | 石药集团中诺药业（石家庄）有限公司 | Crystal form of ceftriaxone sodium and preparation method for crystal form |
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2005
- 2005-10-21 CN CNB2005101182366A patent/CN100335485C/en active Active
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011012965A1 (en) * | 2009-07-27 | 2011-02-03 | Nectar Lifesciences Ltd. | Improved process for preparation of ceftriaxone disodium hemiheptahydrate |
| CN104031067A (en) * | 2014-05-21 | 2014-09-10 | 丽珠医药集团股份有限公司 | Refinement method of ceftriaxone sodium crude product |
| CN104876948A (en) * | 2015-05-28 | 2015-09-02 | 华北制药河北华民药业有限责任公司 | Preparation method of ceftriaxone sodium |
| CN106008554A (en) * | 2016-05-23 | 2016-10-12 | 河南康达制药有限公司 | Preparation method and product of ceftriaxone sodium sterile powder |
| CN106366099A (en) * | 2016-08-22 | 2017-02-01 | 山东罗欣药业集团恒欣药业有限公司 | Anti-infection medicine ceftriaxone sodium crystal compound and preparation method thereof |
| CN110396101A (en) * | 2018-12-03 | 2019-11-01 | 广东金城金素制药有限公司 | Qu Suofen Ceftriaxone Sodium pharmaceutical preparation treats the new indication of bacillary intimitis |
| CN112679524A (en) * | 2020-12-24 | 2021-04-20 | 华北制药河北华民药业有限责任公司 | Preparation method of ceftriaxone sodium |
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| CN100335485C (en) | 2007-09-05 |
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