CN102030751B - 一种盐酸莫西沙星的结晶工艺 - Google Patents
一种盐酸莫西沙星的结晶工艺 Download PDFInfo
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- CN102030751B CN102030751B CN201010572041XA CN201010572041A CN102030751B CN 102030751 B CN102030751 B CN 102030751B CN 201010572041X A CN201010572041X A CN 201010572041XA CN 201010572041 A CN201010572041 A CN 201010572041A CN 102030751 B CN102030751 B CN 102030751B
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- moxifloxacin
- acid salt
- crystallization
- drying
- alkyl oxide
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- 229960005112 moxifloxacin hydrochloride Drugs 0.000 title claims abstract description 45
- IDIIJJHBXUESQI-DFIJPDEKSA-N moxifloxacin hydrochloride Chemical compound Cl.COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 IDIIJJHBXUESQI-DFIJPDEKSA-N 0.000 title claims abstract description 45
- 238000000034 method Methods 0.000 title claims abstract description 29
- 229960003702 moxifloxacin Drugs 0.000 claims abstract description 70
- 238000002425 crystallisation Methods 0.000 claims abstract description 51
- 230000008025 crystallization Effects 0.000 claims abstract description 50
- FABPRXSRWADJSP-MEDUHNTESA-N moxifloxacin Chemical compound COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 FABPRXSRWADJSP-MEDUHNTESA-N 0.000 claims abstract description 43
- -1 glycol alkyl ether Chemical class 0.000 claims abstract description 34
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000002253 acid Substances 0.000 claims abstract description 23
- 150000003839 salts Chemical class 0.000 claims abstract description 18
- 238000001035 drying Methods 0.000 claims abstract description 17
- 239000013078 crystal Substances 0.000 claims abstract description 15
- 238000000967 suction filtration Methods 0.000 claims abstract description 15
- 238000001816 cooling Methods 0.000 claims abstract description 14
- 239000000706 filtrate Substances 0.000 claims abstract description 14
- 238000003756 stirring Methods 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 23
- 238000009413 insulation Methods 0.000 claims description 16
- 238000001291 vacuum drying Methods 0.000 claims description 14
- YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 claims description 10
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 10
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 239000011259 mixed solution Substances 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 5
- 238000004042 decolorization Methods 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 238000004061 bleaching Methods 0.000 claims description 2
- 239000000047 product Substances 0.000 abstract description 13
- 239000002904 solvent Substances 0.000 abstract description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract description 7
- 239000003960 organic solvent Substances 0.000 abstract description 4
- 238000001914 filtration Methods 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 231100000572 poisoning Toxicity 0.000 abstract 1
- 230000000607 poisoning effect Effects 0.000 abstract 1
- 238000004065 wastewater treatment Methods 0.000 abstract 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000001953 recrystallisation Methods 0.000 description 11
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical group CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000845 anti-microbial effect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- PSYGHMBJXWRQFD-UHFFFAOYSA-N 2-(2-sulfanylacetyl)oxyethyl 2-sulfanylacetate Chemical compound SCC(=O)OCCOC(=O)CS PSYGHMBJXWRQFD-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- KSCPLKVBWDOSAI-RQJHMYQMSA-N C1NC[C@@H]2NCCC[C@H]12 Chemical compound C1NC[C@@H]2NCCC[C@H]12 KSCPLKVBWDOSAI-RQJHMYQMSA-N 0.000 description 2
- FABPRXSRWADJSP-BZNIZROVSA-N COc(c(N1C[C@@H]2NCCC[C@@H]2C1)c(cc12)F)c1N(C1CC1)C=C(C(O)=O)C2=O Chemical compound COc(c(N1C[C@@H]2NCCC[C@@H]2C1)c(cc12)F)c1N(C1CC1)C=C(C(O)=O)C2=O FABPRXSRWADJSP-BZNIZROVSA-N 0.000 description 2
- GJCNJYCCBBFZLQ-UHFFFAOYSA-N Cc(c(OC)c(c1c2)N(C3CC3)C=C(C(O)=O)C1=O)c2F Chemical compound Cc(c(OC)c(c1c2)N(C3CC3)C=C(C(O)=O)C1=O)c2F GJCNJYCCBBFZLQ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 235000007244 Zea mays Nutrition 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229960001701 chloroform Drugs 0.000 description 2
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 2
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical group CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 2
- 229940124307 fluoroquinolone Drugs 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229940095064 tartrate Drugs 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- ZYVYEJXMYBUCMN-UHFFFAOYSA-N 1-methoxy-2-methylpropane Chemical compound COCC(C)C ZYVYEJXMYBUCMN-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical group C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 238000005950 photosensitized reaction Methods 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000036228 toxication Effects 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (8)
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CN201010572041XA CN102030751B (zh) | 2010-12-01 | 2010-12-01 | 一种盐酸莫西沙星的结晶工艺 |
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CN201010572041XA CN102030751B (zh) | 2010-12-01 | 2010-12-01 | 一种盐酸莫西沙星的结晶工艺 |
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CN102030751A CN102030751A (zh) | 2011-04-27 |
CN102030751B true CN102030751B (zh) | 2012-11-21 |
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Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102321083B (zh) * | 2011-07-14 | 2013-05-15 | 福建省福抗药业股份有限公司 | 一种无水盐酸莫西沙星晶型f的制备方法 |
CN102344447B (zh) * | 2011-07-20 | 2013-09-18 | 华润赛科药业有限责任公司 | 一种盐酸莫西沙星一水合物晶型及其制备方法 |
CN103183671A (zh) * | 2011-12-29 | 2013-07-03 | 天津康鸿医药科技发展有限公司 | 一种新的盐酸莫西沙星晶体及其制备方法和应用 |
CN103183672A (zh) * | 2011-12-29 | 2013-07-03 | 天津康鸿医药科技发展有限公司 | 一种新的盐酸莫西沙星晶体及其制备方法和应用 |
CN104725377B (zh) * | 2014-04-04 | 2017-06-06 | 江苏天一时制药有限公司 | 一种盐酸莫西沙星的晶型及其制备方法 |
CN104817557B (zh) * | 2014-04-04 | 2017-05-31 | 江苏天一时制药有限公司 | 一种盐酸莫西沙星的稳定晶型及其制备方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1151151C (zh) * | 1997-11-24 | 2004-05-26 | 拜尔公司 | 8-甲氧基-喹诺酮羧酸类的制备方法 |
WO2008059521A2 (en) * | 2006-11-14 | 2008-05-22 | Msn Laboratories Limited | Novel process for the preparation of moxifloxacin hydrochloride and a novel polymorph of moxifloxacin |
CN101817820A (zh) * | 2009-07-30 | 2010-09-01 | 重庆博腾精细化工有限公司 | 一种盐酸莫西沙星的合成方法 |
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2010
- 2010-12-01 CN CN201010572041XA patent/CN102030751B/zh active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1151151C (zh) * | 1997-11-24 | 2004-05-26 | 拜尔公司 | 8-甲氧基-喹诺酮羧酸类的制备方法 |
WO2008059521A2 (en) * | 2006-11-14 | 2008-05-22 | Msn Laboratories Limited | Novel process for the preparation of moxifloxacin hydrochloride and a novel polymorph of moxifloxacin |
CN101817820A (zh) * | 2009-07-30 | 2010-09-01 | 重庆博腾精细化工有限公司 | 一种盐酸莫西沙星的合成方法 |
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Address after: 31 Weisan Road, Shangyu Economic and Technological Development Zone, Hangzhou Bay, Shangyu City, Shaoxing City, Zhejiang Province, China, 312369 Patentee after: Shaoxing Jingxin Pharmaceutical Co.,Ltd. Address before: 31 Weisan Road, Shangyu Industrial Park, Hangzhou Bay, Shangyu City, Shaoxing City, Zhejiang Province, 312300 Patentee before: SHANGYU JINGXIN PHARMACEUTICAL Co.,Ltd. |
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Address after: 312369 No.31, Weisan Road, Shangyu economic and Technological Development Zone, Hangzhou Bay, Shaoxing City, Zhejiang Province Patentee after: Shaoxing Jingxin Pharmaceutical Co.,Ltd. Country or region after: China Address before: 31 Weisan Road, Shangyu Economic and Technological Development Zone, Hangzhou Bay, Shangyu City, Shaoxing City, Zhejiang Province, China, 312369 Patentee before: Shaoxing Jingxin Pharmaceutical Co.,Ltd. Country or region before: China |