CN101891753B - 一种d(-)-磺苄西林钠的制备方法 - Google Patents
一种d(-)-磺苄西林钠的制备方法 Download PDFInfo
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- CN101891753B CN101891753B CN2010102550737A CN201010255073A CN101891753B CN 101891753 B CN101891753 B CN 101891753B CN 2010102550737 A CN2010102550737 A CN 2010102550737A CN 201010255073 A CN201010255073 A CN 201010255073A CN 101891753 B CN101891753 B CN 101891753B
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- Prior art keywords
- sulfocillin
- solution
- preparation
- sulphur
- reaction
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- JETQIUPBHQNHNZ-NJBDSQKTSA-N (2s,5r,6r)-3,3-dimethyl-7-oxo-6-[[(2r)-2-phenyl-2-sulfoacetyl]amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Chemical compound C1([C@H](C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)S(O)(=O)=O)=CC=CC=C1 JETQIUPBHQNHNZ-NJBDSQKTSA-N 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 239000011734 sodium Substances 0.000 title claims abstract description 8
- 229910052708 sodium Inorganic materials 0.000 title claims abstract description 6
- 238000006243 chemical reaction Methods 0.000 claims abstract description 49
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 35
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000012043 crude product Substances 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- NGHVIOIJCVXTGV-ALEPSDHESA-N 6-aminopenicillanic acid Chemical compound [O-]C(=O)[C@H]1C(C)(C)S[C@@H]2[C@H]([NH3+])C(=O)N21 NGHVIOIJCVXTGV-ALEPSDHESA-N 0.000 claims abstract description 20
- NGHVIOIJCVXTGV-UHFFFAOYSA-N 6beta-amino-penicillanic acid Natural products OC(=O)C1C(C)(C)SC2C(N)C(=O)N21 NGHVIOIJCVXTGV-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000002253 acid Substances 0.000 claims abstract description 17
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000012046 mixed solvent Substances 0.000 claims abstract description 9
- 239000012467 final product Substances 0.000 claims abstract description 4
- FWRNIJIOFYDBES-ZQDFAFASSA-L disodium;(2s,5r,6r)-3,3-dimethyl-7-oxo-6-[[(2r)-2-phenyl-2-sulfonatoacetyl]amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate Chemical compound [Na+].[Na+].C1([C@H](C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C([O-])=O)(C)C)S([O-])(=O)=O)=CC=CC=C1 FWRNIJIOFYDBES-ZQDFAFASSA-L 0.000 claims description 50
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 48
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 45
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 35
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 24
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 18
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 16
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 14
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-diisopropylethylamine Substances CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims description 14
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 14
- 238000004821 distillation Methods 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 14
- 229960004756 ethanol Drugs 0.000 claims description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 7
- 229960000935 dehydrated alcohol Drugs 0.000 claims description 7
- 239000012065 filter cake Substances 0.000 claims description 7
- 239000012074 organic phase Substances 0.000 claims description 7
- 230000001105 regulatory effect Effects 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 238000001291 vacuum drying Methods 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- 239000005864 Sulphur Substances 0.000 claims description 5
- 238000000746 purification Methods 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000000047 product Substances 0.000 abstract description 4
- OVAWAJRNDPSGHE-UHFFFAOYSA-N 2-methyloxolane;hydrate Chemical compound O.CC1CCCO1 OVAWAJRNDPSGHE-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 62
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- FWRNIJIOFYDBES-HCIBPFAFSA-L sulbenicillin disodium Chemical compound [Na+].[Na+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)C(S([O-])(=O)=O)C1=CC=CC=C1 FWRNIJIOFYDBES-HCIBPFAFSA-L 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- 150000001263 acyl chlorides Chemical class 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 229930182555 Penicillin Natural products 0.000 description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229940049954 penicillin Drugs 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 150000003952 β-lactams Chemical class 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 241000588769 Proteus <enterobacteria> Species 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 206010040047 Sepsis Diseases 0.000 description 1
- 206010062255 Soft tissue infection Diseases 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 208000013223 septicemia Diseases 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
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CN2010102550737A CN101891753B (zh) | 2010-08-17 | 2010-08-17 | 一种d(-)-磺苄西林钠的制备方法 |
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CN2010102550737A CN101891753B (zh) | 2010-08-17 | 2010-08-17 | 一种d(-)-磺苄西林钠的制备方法 |
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CN101891753A CN101891753A (zh) | 2010-11-24 |
CN101891753B true CN101891753B (zh) | 2011-06-08 |
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Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102210677A (zh) * | 2011-05-04 | 2011-10-12 | 湖南湘药制药有限公司 | 含磺苄西林钠与他唑巴坦类化合物的抗菌组合药 |
CN102161667B (zh) * | 2011-05-05 | 2012-11-21 | 苏州二叶制药有限公司 | 磺苄西林钠及注射用磺苄西林钠 |
CN102924480B (zh) * | 2012-11-15 | 2014-07-30 | 齐鲁天和惠世制药有限公司 | 一种d(-)-磺苄西林钠的制备方法 |
CN103319502B (zh) * | 2013-04-24 | 2015-05-20 | 济南康和医药科技有限公司 | 一种磺苄西林钠的制备方法 |
CN104910179A (zh) * | 2015-05-04 | 2015-09-16 | 湖南尔康湘药制药有限公司 | 一种注射用磺苄西林钠的制备方法 |
CN105218562A (zh) * | 2015-09-30 | 2016-01-06 | 浙江汇能动物药品有限公司 | 一种d(-)-磺苄西林钠的制备方法 |
CN107641130B (zh) * | 2017-07-13 | 2020-05-29 | 中国医药集团总公司四川抗菌素工业研究所 | 一种d-磺苄西林钠的制备方法 |
CN113980033B (zh) * | 2021-11-03 | 2023-02-28 | 海南海灵化学制药有限公司 | 一种d-磺苄西林钠的合成工艺 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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AT290728B (de) * | 1968-09-28 | 1971-05-15 | Takeda Chemical Industries Ltd | Verfahren zur herstellung neuer penicilline |
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Owner name: CHANGSHA HUAMEI MEDICAL TECHNOLOGY CO., LTD. |
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Effective date of registration: 20110428 Address after: 410331 Liuyang biological medicine Park, Hunan, Changsha Applicant after: HUNAN SANQING PHARMACEUTICAL Co.,Ltd. Co-applicant after: CHANGSHA HUAMEI MEDICINE SCIENCE & TECHNOLOGY Co.,Ltd. Address before: 410331 Liuyang biological medicine Park, Hunan, Changsha Applicant before: HUNAN SANQING PHARMACEUTICAL Co.,Ltd. |
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Application publication date: 20101124 Assignee: HUNAN SANQING PHARMACEUTICAL Co.,Ltd. Assignor: HUNAN SANQING PHARMACEUTICAL Co.,Ltd.|CHANGSHA HUAMEI MEDICINE SCIENCE & TECHNOLOGY Co.,Ltd. Contract record no.: 2013430000166 Denomination of invention: Method for preparing D (-) - benzyl penicillin sodium Granted publication date: 20110608 License type: Exclusive License Record date: 20131014 |
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CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20110608 Termination date: 20210817 |
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