CN101928214B - 右旋酮洛芬氨丁三醇的一种合成方法 - Google Patents
右旋酮洛芬氨丁三醇的一种合成方法 Download PDFInfo
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- CN101928214B CN101928214B CN 200910062741 CN200910062741A CN101928214B CN 101928214 B CN101928214 B CN 101928214B CN 200910062741 CN200910062741 CN 200910062741 CN 200910062741 A CN200910062741 A CN 200910062741A CN 101928214 B CN101928214 B CN 101928214B
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- Prior art keywords
- dexketoprofen
- cooled
- octylglucamine
- centrifugal
- purified water
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- 238000000034 method Methods 0.000 title claims abstract description 21
- QUZMDHVOUNDEKW-MERQFXBCSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;(2s)-2-(3-benzoylphenyl)propanoic acid Chemical compound OCC(N)(CO)CO.OC(=O)[C@@H](C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 QUZMDHVOUNDEKW-MERQFXBCSA-N 0.000 title claims abstract description 19
- 229960005448 dexketoprofen trometamol Drugs 0.000 title claims abstract description 19
- 230000002194 synthesizing effect Effects 0.000 title abstract 2
- ZRRNJJURLBXWLL-REWJHTLYSA-N (2r,3r,4r,5s)-6-(octylamino)hexane-1,2,3,4,5-pentol Chemical compound CCCCCCCCNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO ZRRNJJURLBXWLL-REWJHTLYSA-N 0.000 claims abstract description 37
- DKYWVDODHFEZIM-NSHDSACASA-N dexketoprofen Chemical class OC(=O)[C@@H](C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-NSHDSACASA-N 0.000 claims abstract description 22
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229960000281 trometamol Drugs 0.000 claims abstract description 10
- 239000013078 crystal Substances 0.000 claims abstract description 9
- 238000007670 refining Methods 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 75
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 49
- 239000008213 purified water Substances 0.000 claims description 43
- 239000012065 filter cake Substances 0.000 claims description 42
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 40
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 39
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 36
- 238000005406 washing Methods 0.000 claims description 33
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 32
- 229960002783 dexketoprofen Drugs 0.000 claims description 30
- 238000003756 stirring Methods 0.000 claims description 25
- 238000001035 drying Methods 0.000 claims description 21
- 239000012452 mother liquor Substances 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 16
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 16
- 239000012085 test solution Substances 0.000 claims description 16
- 238000002425 crystallisation Methods 0.000 claims description 15
- 230000008025 crystallization Effects 0.000 claims description 15
- 238000010792 warming Methods 0.000 claims description 14
- 238000004821 distillation Methods 0.000 claims description 13
- -1 dexketoprofen N-Octylglucamine salt Chemical class 0.000 claims description 12
- 239000006210 lotion Substances 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 12
- 238000011084 recovery Methods 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 10
- 239000000047 product Substances 0.000 claims description 9
- 235000021463 dry cake Nutrition 0.000 claims description 8
- 238000001914 filtration Methods 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 235000019441 ethanol Nutrition 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 5
- 238000013019 agitation Methods 0.000 claims description 4
- 238000005267 amalgamation Methods 0.000 claims description 4
- 235000012970 cakes Nutrition 0.000 claims description 4
- 238000005352 clarification Methods 0.000 claims description 4
- 239000002826 coolant Substances 0.000 claims description 4
- 238000001514 detection method Methods 0.000 claims description 4
- 238000003810 ethyl acetate extraction Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- 238000001953 recrystallisation Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- 229940002612 prodrug Drugs 0.000 abstract description 3
- 239000000651 prodrug Substances 0.000 abstract description 3
- 238000009776 industrial production Methods 0.000 abstract description 2
- 239000012046 mixed solvent Substances 0.000 abstract description 2
- 230000006340 racemization Effects 0.000 abstract description 2
- 150000003839 salts Chemical class 0.000 abstract 3
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 abstract 2
- 229960000991 ketoprofen Drugs 0.000 abstract 2
- 238000000926 separation method Methods 0.000 abstract 1
- 238000009833 condensation Methods 0.000 description 10
- 230000005494 condensation Effects 0.000 description 10
- 206010013786 Dry skin Diseases 0.000 description 7
- 239000012266 salt solution Substances 0.000 description 6
- 208000002193 Pain Diseases 0.000 description 5
- 230000000202 analgesic effect Effects 0.000 description 3
- 230000036407 pain Effects 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 2
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 229940025084 amphetamine Drugs 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 230000001754 anti-pyretic effect Effects 0.000 description 2
- 239000002221 antipyretic Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 206010002556 Ankylosing Spondylitis Diseases 0.000 description 1
- 206010058019 Cancer Pain Diseases 0.000 description 1
- 208000000094 Chronic Pain Diseases 0.000 description 1
- 208000034656 Contusions Diseases 0.000 description 1
- 206010013935 Dysmenorrhoea Diseases 0.000 description 1
- 206010024453 Ligament sprain Diseases 0.000 description 1
- 208000004550 Postoperative Pain Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 208000010040 Sprains and Strains Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 208000005298 acute pain Diseases 0.000 description 1
- 230000036592 analgesia Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000009519 contusion Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 210000004872 soft tissue Anatomy 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 208000004371 toothache Diseases 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN 200910062741 CN101928214B (zh) | 2009-06-19 | 2009-06-19 | 右旋酮洛芬氨丁三醇的一种合成方法 |
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CN 200910062741 CN101928214B (zh) | 2009-06-19 | 2009-06-19 | 右旋酮洛芬氨丁三醇的一种合成方法 |
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Publication Number | Publication Date |
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CN101928214A CN101928214A (zh) | 2010-12-29 |
CN101928214B true CN101928214B (zh) | 2012-12-19 |
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Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102850204B (zh) * | 2011-06-29 | 2015-08-19 | 徐州医学院 | 一种(s)-2-芳基丙酸类非甾体抗炎药的拆分方法 |
CN102381986A (zh) * | 2011-07-25 | 2012-03-21 | 南京特丰药业股份有限公司 | 一种右旋布洛芬氨丁三醇盐及其口服溶液的制备方法 |
CN102743341B (zh) * | 2012-07-28 | 2014-02-26 | 西安德天药业股份有限公司 | 右旋酮洛芬氨丁三醇缓释微粒及其制备方法和缓释制剂 |
CN109096229A (zh) * | 2018-08-29 | 2018-12-28 | 南京正科医药股份有限公司 | 一种右旋酮洛芬中间体的合成方法 |
CN115607509B (zh) * | 2022-10-11 | 2024-01-30 | 南京正科医药股份有限公司 | 一种右旋酮洛芬氨丁三醇注射液及其制备工艺 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5554789A (en) * | 1992-11-10 | 1996-09-10 | Laboratorios Menarini S.A. | Arylpropionic derivative, a process for the preparation and the use thereof as an analgesic agent |
US5808069A (en) * | 1993-03-09 | 1998-09-15 | Dompe' Farmaceutici Spa | Salts of 2-(3-benzoylphenyl) propionic acid with organic bases and pharmaceutical compositions thereof |
CN1349970A (zh) * | 2001-11-02 | 2002-05-22 | 中国科学院上海有机化学研究所 | 2-(3-苯甲酰基苯基)丙酸的对映体的制备方法 |
CN1418886A (zh) * | 2002-12-03 | 2003-05-21 | 中国人民解放军第四军医大学第一附属医院 | 右酮洛芬葡辛胺盐及制备方法和以该活性成分的药物组合物 |
-
2009
- 2009-06-19 CN CN 200910062741 patent/CN101928214B/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5554789A (en) * | 1992-11-10 | 1996-09-10 | Laboratorios Menarini S.A. | Arylpropionic derivative, a process for the preparation and the use thereof as an analgesic agent |
US5808069A (en) * | 1993-03-09 | 1998-09-15 | Dompe' Farmaceutici Spa | Salts of 2-(3-benzoylphenyl) propionic acid with organic bases and pharmaceutical compositions thereof |
CN1349970A (zh) * | 2001-11-02 | 2002-05-22 | 中国科学院上海有机化学研究所 | 2-(3-苯甲酰基苯基)丙酸的对映体的制备方法 |
CN1418886A (zh) * | 2002-12-03 | 2003-05-21 | 中国人民解放军第四军医大学第一附属医院 | 右酮洛芬葡辛胺盐及制备方法和以该活性成分的药物组合物 |
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CN101928214A (zh) | 2010-12-29 |
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C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A Synthesis Method of D-Ketoprofen Aminobutanol Triol Effective date of registration: 20230421 Granted publication date: 20121219 Pledgee: Bank of China Limited Huangshi Branch Pledgor: HUANGSHI SHIXING PHARMACEUTICAL Co.,Ltd. Registration number: Y2023420000174 |
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Granted publication date: 20121219 Pledgee: Bank of China Limited Huangshi Branch Pledgor: HUANGSHI SHIXING PHARMACEUTICAL Co.,Ltd. Registration number: Y2023420000174 |
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PC01 | Cancellation of the registration of the contract for pledge of patent right | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A synthetic method of D-ketoprofen tromethamine Granted publication date: 20121219 Pledgee: Bank of China Limited Huangshi Branch Pledgor: HUANGSHI SHIXING PHARMACEUTICAL Co.,Ltd. Registration number: Y2024980013802 |
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