CN114213350B - 一种他汀类药物中间体的制备方法 - Google Patents
一种他汀类药物中间体的制备方法 Download PDFInfo
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- CN114213350B CN114213350B CN202111630044.9A CN202111630044A CN114213350B CN 114213350 B CN114213350 B CN 114213350B CN 202111630044 A CN202111630044 A CN 202111630044A CN 114213350 B CN114213350 B CN 114213350B
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- reaction
- compound
- permanganate
- oxidant
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- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 title claims abstract description 14
- 239000003814 drug Substances 0.000 title claims abstract description 10
- 229940079593 drug Drugs 0.000 title claims abstract description 10
- 239000007800 oxidant agent Substances 0.000 claims abstract description 40
- 230000001590 oxidative effect Effects 0.000 claims abstract description 39
- 239000012286 potassium permanganate Substances 0.000 claims abstract description 20
- JZCCFEFSEZPSOG-UHFFFAOYSA-L copper(II) sulfate pentahydrate Chemical compound O.O.O.O.O.[Cu+2].[O-]S([O-])(=O)=O JZCCFEFSEZPSOG-UHFFFAOYSA-L 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims description 41
- 239000000843 powder Substances 0.000 claims description 9
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims description 9
- 235000019345 sodium thiosulphate Nutrition 0.000 claims description 9
- 238000005406 washing Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- 230000035484 reaction time Effects 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 2
- 239000000543 intermediate Substances 0.000 abstract description 9
- 239000000203 mixture Substances 0.000 abstract description 4
- 239000002904 solvent Substances 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 239000004570 mortar (masonry) Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- CABVTRNMFUVUDM-VRHQGPGLSA-N (3S)-3-hydroxy-3-methylglutaryl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C[C@@](O)(CC(O)=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 CABVTRNMFUVUDM-VRHQGPGLSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 102000007330 LDL Lipoproteins Human genes 0.000 description 2
- 108010007622 LDL Lipoproteins Proteins 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- KJTLQQUUPVSXIM-ZCFIWIBFSA-N (R)-mevalonic acid Chemical compound OCC[C@](O)(C)CC(O)=O KJTLQQUUPVSXIM-ZCFIWIBFSA-N 0.000 description 1
- 102100029077 3-hydroxy-3-methylglutaryl-coenzyme A reductase Human genes 0.000 description 1
- 101710158485 3-hydroxy-3-methylglutaryl-coenzyme A reductase Proteins 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- KJTLQQUUPVSXIM-UHFFFAOYSA-N DL-mevalonic acid Natural products OCCC(O)(C)CC(O)=O KJTLQQUUPVSXIM-UHFFFAOYSA-N 0.000 description 1
- 102000000853 LDL receptors Human genes 0.000 description 1
- 108010001831 LDL receptors Proteins 0.000 description 1
- QGAVSDVURUSLQK-UHFFFAOYSA-N ammonium heptamolybdate Chemical compound N.N.N.N.N.N.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[Mo].[Mo].[Mo].[Mo].[Mo].[Mo].[Mo] QGAVSDVURUSLQK-UHFFFAOYSA-N 0.000 description 1
- 208000026106 cerebrovascular disease Diseases 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 210000003494 hepatocyte Anatomy 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
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CN202111630044.9A CN114213350B (zh) | 2021-12-29 | 2021-12-29 | 一种他汀类药物中间体的制备方法 |
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CN202111630044.9A CN114213350B (zh) | 2021-12-29 | 2021-12-29 | 一种他汀类药物中间体的制备方法 |
Publications (2)
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CN114213350A CN114213350A (zh) | 2022-03-22 |
CN114213350B true CN114213350B (zh) | 2024-03-19 |
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CN202111630044.9A Active CN114213350B (zh) | 2021-12-29 | 2021-12-29 | 一种他汀类药物中间体的制备方法 |
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1436174A (zh) * | 2000-06-15 | 2003-08-13 | 布里斯托尔-迈尔斯斯奎布公司 | HMG-CoA还原酶抑制剂及其作为治疗与胆固醇相关疾病的药物的应用 |
CN1436192A (zh) * | 2000-06-15 | 2003-08-13 | 布里斯托尔-迈尔斯斯奎布公司 | HMG-CoA还原酶抑制剂及方法 |
CN1656077A (zh) * | 2001-06-06 | 2005-08-17 | 布里斯托尔-迈尔斯斯奎布公司 | 制备手性二醇砜和二羟基酸HMGCoA还原酶抑制剂的方法 |
CN103328470A (zh) * | 2011-01-18 | 2013-09-25 | 中化帝斯曼制药有限公司荷兰公司 | 制备二醇砜的方法 |
CN103360384A (zh) * | 2013-07-30 | 2013-10-23 | 浙江京新药业股份有限公司 | HMG-CoA还原酶抑制剂关键中间体的合成方法 |
CN103649068A (zh) * | 2011-07-19 | 2014-03-19 | 广东东阳光药业有限公司 | 一种他汀类药物中间体和其制备方法 |
CN107245072A (zh) * | 2016-11-18 | 2017-10-13 | 河南师范大学 | 一种厄洛替尼‑1,2,3‑三氮唑类化合物的制备方法 |
CN110627736A (zh) * | 2019-09-26 | 2019-12-31 | 江苏阿尔法药业有限公司 | 一种1-苯基-5-羟基四氮唑的回收利用方法 |
-
2021
- 2021-12-29 CN CN202111630044.9A patent/CN114213350B/zh active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1436174A (zh) * | 2000-06-15 | 2003-08-13 | 布里斯托尔-迈尔斯斯奎布公司 | HMG-CoA还原酶抑制剂及其作为治疗与胆固醇相关疾病的药物的应用 |
CN1436192A (zh) * | 2000-06-15 | 2003-08-13 | 布里斯托尔-迈尔斯斯奎布公司 | HMG-CoA还原酶抑制剂及方法 |
CN1656077A (zh) * | 2001-06-06 | 2005-08-17 | 布里斯托尔-迈尔斯斯奎布公司 | 制备手性二醇砜和二羟基酸HMGCoA还原酶抑制剂的方法 |
CN103328470A (zh) * | 2011-01-18 | 2013-09-25 | 中化帝斯曼制药有限公司荷兰公司 | 制备二醇砜的方法 |
CN103649068A (zh) * | 2011-07-19 | 2014-03-19 | 广东东阳光药业有限公司 | 一种他汀类药物中间体和其制备方法 |
CN103360384A (zh) * | 2013-07-30 | 2013-10-23 | 浙江京新药业股份有限公司 | HMG-CoA还原酶抑制剂关键中间体的合成方法 |
CN107245072A (zh) * | 2016-11-18 | 2017-10-13 | 河南师范大学 | 一种厄洛替尼‑1,2,3‑三氮唑类化合物的制备方法 |
CN110627736A (zh) * | 2019-09-26 | 2019-12-31 | 江苏阿尔法药业有限公司 | 一种1-苯基-5-羟基四氮唑的回收利用方法 |
Non-Patent Citations (1)
Title |
---|
Selective oxidation of sulfides under solvent-free conditions;Shaabani, Ahmad,等;Sulfur Letters;第26卷(第2期);43-45 * |
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CN114213350A (zh) | 2022-03-22 |
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Address after: 223800 Suqian Eco-chemical Science and Technology Industrial Park, Suqian City, Jiangsu Province Patentee after: Jiangsu Alpha Group Furui Pharmaceutical (Suqian) Co.,Ltd. Country or region after: China Address before: 223800 Suqian Eco-chemical Science and Technology Industrial Park, Suqian City, Jiangsu Province Patentee before: Jiangsu Furui Kangtai Pharmaceutical Co.,Ltd. Country or region before: China |
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PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A preparation method for intermediate of statin drugs Granted publication date: 20240319 Pledgee: Industrial Bank Co.,Ltd. Suqian Branch Pledgor: Jiangsu Alpha Group Furui Pharmaceutical (Suqian) Co.,Ltd. Registration number: Y2024980014609 |