PH25960A - Dextro-rotatory enantiomer of methyl alpha-5-(4,5-6,7-tetrahydro (3,2-C) thieno pyridyl (2-chloro-phenyl) acetate and the pharmaceutical compositions containing it - Google Patents
Dextro-rotatory enantiomer of methyl alpha-5-(4,5-6,7-tetrahydro (3,2-C) thieno pyridyl (2-chloro-phenyl) acetate and the pharmaceutical compositions containing it Download PDFInfo
- Publication number
- PH25960A PH25960A PH36488A PH36488A PH25960A PH 25960 A PH25960 A PH 25960A PH 36488 A PH36488 A PH 36488A PH 36488 A PH36488 A PH 36488A PH 25960 A PH25960 A PH 25960A
- Authority
- PH
- Philippines
- Prior art keywords
- rotatory
- dextro
- tetrahydro
- pyridyl
- methyl alpha
- Prior art date
Links
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 title claims description 20
- 239000008194 pharmaceutical composition Substances 0.000 title description 4
- -1 thieno pyridyl (2-chloro-phenyl) acetate Chemical compound 0.000 title description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 54
- 150000003839 salts Chemical class 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 23
- 125000004588 thienopyridyl group Chemical group S1C(=CC2=C1C=CC=N2)* 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 17
- CJPVPOYTTALCNX-UHFFFAOYSA-N (2-chlorophenyl) acetate Chemical compound CC(=O)OC1=CC=CC=C1Cl CJPVPOYTTALCNX-UHFFFAOYSA-N 0.000 claims description 13
- 230000003287 optical effect Effects 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 29
- 239000013078 crystal Substances 0.000 description 21
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 18
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 239000002904 solvent Substances 0.000 description 17
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 16
- 230000002776 aggregation Effects 0.000 description 14
- 238000004220 aggregation Methods 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- 239000000047 product Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 9
- 238000001953 recrystallisation Methods 0.000 description 9
- 235000017557 sodium bicarbonate Nutrition 0.000 description 9
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- DTGLZDAWLRGWQN-UHFFFAOYSA-N prasugrel Chemical compound C1CC=2SC(OC(=O)C)=CC=2CN1C(C=1C(=CC=CC=1)F)C(=O)C1CC1 DTGLZDAWLRGWQN-UHFFFAOYSA-N 0.000 description 8
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 229910052761 rare earth metal Inorganic materials 0.000 description 7
- 150000002910 rare earth metals Chemical class 0.000 description 7
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 7
- 230000002401 inhibitory effect Effects 0.000 description 6
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 231100000419 toxicity Toxicity 0.000 description 4
- 230000001988 toxicity Effects 0.000 description 4
- 244000215068 Acacia senegal Species 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 102000008186 Collagen Human genes 0.000 description 3
- 108010035532 Collagen Proteins 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 230000005526 G1 to G0 transition Effects 0.000 description 3
- 229920000084 Gum arabic Polymers 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241000700159 Rattus Species 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 239000000205 acacia gum Substances 0.000 description 3
- 235000010489 acacia gum Nutrition 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- MIOPJNTWMNEORI-UHFFFAOYSA-N camphorsulfonic acid Chemical compound C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C MIOPJNTWMNEORI-UHFFFAOYSA-N 0.000 description 3
- 229920001429 chelating resin Polymers 0.000 description 3
- 229920001436 collagen Polymers 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 235000019359 magnesium stearate Nutrition 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000000829 suppository Substances 0.000 description 3
- WBWWGRHZICKQGZ-HZAMXZRMSA-N taurocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@@H](O)C1 WBWWGRHZICKQGZ-HZAMXZRMSA-N 0.000 description 3
- GAQWDBUWBUOFLS-UHFFFAOYSA-N (7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl)methanesulfonic acid;hydrate Chemical compound O.C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C GAQWDBUWBUOFLS-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- 235000019759 Maize starch Nutrition 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- WBWWGRHZICKQGZ-UHFFFAOYSA-N Taurocholic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(=O)NCCS(O)(=O)=O)C)C1(C)C(O)C2 WBWWGRHZICKQGZ-UHFFFAOYSA-N 0.000 description 2
- 206010047249 Venous thrombosis Diseases 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000004931 aggregating effect Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000002785 anti-thrombosis Effects 0.000 description 2
- JTMZBRWRXFAITF-UHFFFAOYSA-N azane;(7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl)methanesulfonic acid Chemical compound [NH4+].C1CC2(CS([O-])(=O)=O)C(=O)CC1C2(C)C JTMZBRWRXFAITF-UHFFFAOYSA-N 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000008298 dragée Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 150000003840 hydrochlorides Chemical class 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229940102223 injectable solution Drugs 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 210000004623 platelet-rich plasma Anatomy 0.000 description 2
- 239000011736 potassium bicarbonate Substances 0.000 description 2
- 235000015497 potassium bicarbonate Nutrition 0.000 description 2
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 2
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 239000007940 sugar coated tablet Substances 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- 210000003462 vein Anatomy 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical class CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
- IKQCSJBQLWJEPU-UHFFFAOYSA-N 2,5-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=C(O)C(S(O)(=O)=O)=C1 IKQCSJBQLWJEPU-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- 208000037260 Atherosclerotic Plaque Diseases 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 208000013544 Platelet disease Diseases 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 210000000702 aorta abdominal Anatomy 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004106 carminic acid Substances 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 229940082483 carnauba wax Drugs 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- FDEODCTUSIWGLK-RSAXXLAASA-N clopidogrel sulfate Chemical compound [H+].OS([O-])(=O)=O.C1([C@H](N2CC=3C=CSC=3CC2)C(=O)OC)=CC=CC=C1Cl FDEODCTUSIWGLK-RSAXXLAASA-N 0.000 description 1
- 229940080423 cochineal Drugs 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940049636 dobesilic acid Drugs 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229960001031 glucose Drugs 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 210000003111 iliac vein Anatomy 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 231100000518 lethal Toxicity 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057948 magnesium stearate Drugs 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229940056211 paraffin Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 229960001412 pentobarbital Drugs 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000012453 sprague-dawley rat model Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000041 toxicology testing Toxicity 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
- C07J41/0061—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives one of the carbon atoms being part of an amide group
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8702025A FR2612929B1 (fr) | 1987-02-17 | 1987-02-17 | Enantiomere dextrogyre de 1a-(tetrahydro- 4,5,6,7 thieno (3,2-c) pyridyl-5) (chloro-2 phenyl)-acetate de methyle, son procede de preparation et les compositions pharmaceutiques le renfermant |
| FR878716516A FR2623810B2 (fr) | 1987-02-17 | 1987-11-27 | Sels de l'alpha-(tetrahydro-4,5,6,7 thieno(3,2-c) pyridyl-5) (chloro-2 phenyl) -acetate de methyle dextrogyre et compositions pharmaceutiques en contenant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH25960A true PH25960A (en) | 1992-01-13 |
Family
ID=26225786
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH36488A PH25960A (en) | 1987-02-17 | 1988-02-11 | Dextro-rotatory enantiomer of methyl alpha-5-(4,5-6,7-tetrahydro (3,2-C) thieno pyridyl (2-chloro-phenyl) acetate and the pharmaceutical compositions containing it |
Country Status (36)
| Country | Link |
|---|---|
| US (1) | US4847265A (ja) |
| EP (1) | EP0281459B1 (ja) |
| JP (1) | JPH0645622B2 (ja) |
| KR (1) | KR960003615B1 (ja) |
| AR (1) | AR243891A1 (ja) |
| AT (1) | ATE121745T1 (ja) |
| AU (1) | AU597784B2 (ja) |
| CA (1) | CA1336777C (ja) |
| CS (1) | CS274420B2 (ja) |
| CY (1) | CY2087B1 (ja) |
| DE (2) | DE19875053I2 (ja) |
| DK (1) | DK173636B1 (ja) |
| ES (1) | ES2071621T4 (ja) |
| FI (1) | FI87216C (ja) |
| FR (1) | FR2623810B2 (ja) |
| HK (1) | HK1000093A1 (ja) |
| HR (1) | HRP920923B1 (ja) |
| HU (2) | HU197909B (ja) |
| IE (1) | IE66922B1 (ja) |
| IL (1) | IL85294A (ja) |
| LU (1) | LU90324I2 (ja) |
| LV (1) | LV5804B4 (ja) |
| MA (1) | MA21184A1 (ja) |
| MX (1) | MX9203026A (ja) |
| MY (1) | MY103198A (ja) |
| NL (1) | NL990002I1 (ja) |
| NO (2) | NO165924C (ja) |
| NZ (1) | NZ223475A (ja) |
| OA (1) | OA08808A (ja) |
| PH (1) | PH25960A (ja) |
| PL (1) | PL156689B1 (ja) |
| PT (1) | PT86726B (ja) |
| RO (1) | RO99191B1 (ja) |
| SI (1) | SI8810231A8 (ja) |
| TN (1) | TNSN88012A1 (ja) |
| YU (1) | YU46748B (ja) |
Families Citing this family (138)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3065421A (en) * | 1957-05-21 | 1962-11-20 | John M Hart | Radio-telephone communication system having means for automatic direct dispatch between mobile stations |
| US3009149A (en) * | 1957-09-30 | 1961-11-14 | Mcdonald Ramsey | Automatic dial radio telephone system |
| US3105118A (en) * | 1960-04-13 | 1963-09-24 | Ericsson Telefon Ab L M | Mobile radio stations interconnected with a wire telephone system |
| US4906756A (en) * | 1988-05-10 | 1990-03-06 | Syntex (U.S.A.) Inc. | 2-(2-nitrovinyl)thiophene reduction and synthesis of thieno[3,2-c]pyridine derivatives |
| GB8824400D0 (en) * | 1988-10-18 | 1988-11-23 | Glaxo Group Ltd | Chemical compounds |
| FR2664596B1 (fr) * | 1990-07-10 | 1994-06-10 | Sanofi Sa | Procede de preparation d'un derive n-phenylacetique de tetrahydrothieno [3,2-c] pyridine et son intermediaire de synthese. |
| FR2672801B1 (fr) * | 1991-02-14 | 1995-03-03 | Sanofi Sa | Utilisation de derives de tetrahydrothienopyridine comme inhibiteurs de l'angiogenese. |
| NZ334389A (en) * | 1996-08-28 | 2001-05-25 | Ube Industries | Cyclic amine derivatives |
| HU225504B1 (en) | 1997-05-13 | 2007-01-29 | Sanofi Aventis | Novel halophenyl-(2-(2-thienyl)-ethylamino)-acetonitriles and process for producing them |
| HU225503B1 (en) * | 1997-05-13 | 2007-01-29 | Sanofi Aventis | Novel 2-(2-halophenyl)-2-(2-(2-thienyl)-ethylamino)-acetamides and process for producing them |
| HU222283B1 (hu) | 1997-05-13 | 2003-05-28 | Sanofi-Synthelabo | Eljárás tieno[3,2-c]piridin-származékok előállítására |
| FR2769313B1 (fr) * | 1997-10-06 | 2000-04-21 | Sanofi Sa | Derives d'esters hydroxyacetiques, leur procede de preparation et leur utilisation comme intermediaires de synthese |
| FR2779726B1 (fr) * | 1998-06-15 | 2001-05-18 | Sanofi Sa | Forme polymorphe de l'hydrogenosulfate de clopidogrel |
| JP4588877B2 (ja) | 1998-06-17 | 2010-12-01 | ブリストル−マイヤーズ スクイブ カンパニー | Ａｄｐ−受容体抗血小板物質と抗高血圧薬の組合せ投与による脳梗塞の予防 |
| FR2792836B3 (fr) | 1999-04-30 | 2001-07-27 | Sanofi Sa | Composition pharmaceutique sous forme unitaire contenant de l'aspirine et de l'hydrogenosulfate de clopidogrel |
| ATE349451T1 (de) * | 2001-01-24 | 2007-01-15 | Cadila Healthcare Ltd | Verfahren zur herstellung von clopidogrel |
| IN191030B (ja) * | 2001-01-24 | 2003-09-13 | Cadila Healthcare Ltd | |
| US6495691B1 (en) | 2001-07-06 | 2002-12-17 | Brantford Chemicals Inc. | Process for the preparation of tetrahydrothieno[3,2-c]pyridine derivatives |
| GB0125708D0 (en) * | 2001-10-26 | 2001-12-19 | Generics Uk Ltd | Novel compounds and processes |
| CA2363053C (en) | 2001-11-09 | 2011-01-25 | Bernard Charles Sherman | Clopidogrel bisulfate tablet formulation |
| AU2002366383B2 (en) * | 2001-12-18 | 2007-06-14 | Teva Pharmaceutical Industries Ltd. | Polymorphs of clopidogrel hydrogensulfate |
| US6767913B2 (en) | 2001-12-18 | 2004-07-27 | Teva Pharmaceutical Industries Ltd. | Crystal forms iii, iv, v, and novel amorphous form of clopidogrel hydrogensulfate, processes for their preparation, processes for the preparation of form i, compositions containing the new forms and methods of administering the new forms |
| US7074928B2 (en) | 2002-01-11 | 2006-07-11 | Teva Pharmaceutical Industries, Ltd. | Polymorphs of clopidogrel hydrogensulfate |
| HUP0200438A3 (en) * | 2002-02-06 | 2003-10-28 | Egis Gyogyszergyar Nyilvanosan | Novel clopidogrel hydrochloride polymorphs, process for the preparation thereof, their use and pharmaceutical compositions containing them |
| ES2357876T3 (es) | 2002-04-16 | 2011-05-03 | Schering Corporation | Antagonistas triciclicos del receptor de trombina. |
| US6800759B2 (en) * | 2002-08-02 | 2004-10-05 | Teva Pharmaceutical Industries Ltd. | Racemization and enantiomer separation of clopidogrel |
| IL166593A0 (en) | 2002-08-02 | 2006-01-15 | Racemization and enantiomer separation of clopidogrel | |
| CZ297472B6 (cs) | 2002-08-27 | 2006-12-13 | Zentiva, A.S. | Zpusob výroby clopidogrelu hydrogensulfátu krystalické formy I |
| AU2003270861A1 (en) * | 2002-10-02 | 2004-04-23 | Bristol-Myers Squibb Company | Novel combination of a factor xa inhibitor and clopidogrel |
| US6812363B2 (en) * | 2002-10-15 | 2004-11-02 | Usv Limited | Racemization of optically active 2-substituted phenyl glycine esters |
| ITMI20022228A1 (it) * | 2002-10-21 | 2004-04-22 | Dinamite Dipharma S P A | Sali di clopidogrel con acidi alchil-solforici. |
| WO2004048385A2 (en) * | 2002-11-28 | 2004-06-10 | Instytut Farmaceutyczny | A process for the preparation of crystalline form 1 or clopidogrel hydrogen sulfate |
| EP1606231A1 (en) * | 2003-02-03 | 2005-12-21 | Nadkarni, Sunil Sadanand | Process for preparation of clopidogrel, its salts and pharmaceutical compositions |
| DE10305984A1 (de) | 2003-02-13 | 2004-09-02 | Helm Ag | Salze organischer Säuren mit Clopidogrel und deren Verwendung zur Herstellung phamazeutischer Formulierungen |
| US7872019B2 (en) * | 2003-03-12 | 2011-01-18 | Cadila Healthcare Limited | Polymorphs and amorphous form of (S)-(+)-clopidogrel bisulfate |
| US6858734B2 (en) * | 2003-04-23 | 2005-02-22 | Rhodia Pharma Solutions Inc. | Preparation of (S)-Clopidogrel and related compounds |
| DE04770646T1 (de) | 2003-04-25 | 2011-12-08 | Cadila Healthcare Ltd. | Salze von clopidogrel und herstellungsverfahren |
| EP1644381B1 (en) * | 2003-07-02 | 2010-03-17 | EGIS Gyógyszergyár Nyilvánosan Müködõ Részvénytársaság | Process for the preparation of crystalline polymorph of a platelet aggregation inhibitor drug |
| CA2530446A1 (en) * | 2003-07-02 | 2005-01-13 | Egis Gyogyszergyar Rt. | Process for the preparation of amorphous form of a platelet aggregation inhibitor drug |
| DE10337773A1 (de) * | 2003-08-13 | 2005-03-24 | Krka Tovarna Zdravil, D.D. | Kristallisation von festen Formen von Clopidogrel-Additionssalzen |
| GB0321256D0 (en) | 2003-09-11 | 2003-10-08 | Generics Uk Ltd | Novel crystalline compounds |
| AU2008200919B2 (en) * | 2003-09-11 | 2009-05-21 | Generics (Uk) Limited | Novel crystalline polymorphs of clopidogrel |
| WO2005063708A2 (en) * | 2003-11-03 | 2005-07-14 | Cadila Healthcare Limited | Processes for preparing different forms of (s)-(+)- clopidogrel bisulfate |
| CA2454015C (en) * | 2003-12-23 | 2009-11-24 | Brantford Chemicals Inc. | A process for the preparation of tetrahydrothieno [3,2-c] pyridine derivatives |
| CA2457459A1 (en) * | 2004-02-11 | 2005-08-11 | Brantford Chemicals Inc. | Resolution of racemates of methyl alpha-5-(4,5,6,7-tetrahydro(3,2-c)thienopyridyl)-(2-chlorophenyl) acetate |
| EP1720884A1 (de) * | 2004-02-24 | 2006-11-15 | Siegfried Generics International AG | Pharmakologisch akzeptierbare salze von clopidogrel |
| EP1723141A4 (en) * | 2004-03-05 | 2007-10-10 | Ipca Lab Ltd | MOST TECHNICAL PROCESS FOR THE PREPARATION OF CLOPIDOGRAPHYDROGENSULFATE |
| TW200534879A (en) * | 2004-03-25 | 2005-11-01 | Bristol Myers Squibb Co | Coated tablet formulation and method |
| KR100563455B1 (ko) * | 2004-04-09 | 2006-03-23 | 한미약품 주식회사 | 결정성 클로피도그렐 나프탈렌술폰산염 또는 이의 수화물,이의 제조방법 및 이를 함유하는 약학적 조성물 |
| CN1938319B (zh) * | 2004-04-09 | 2010-05-12 | 韩美药品株式会社 | 结晶氯吡格雷萘磺酸盐或其水合物、其制备方法及含其的药物组合物 |
| HUE029459T2 (en) * | 2004-04-19 | 2017-02-28 | Krka Tovarna Zdravil D D Novo Mesto | Methods for the Preparation of Polymorph Form I of Clopidogrel Hydrogen Sulphate |
| EP1740594A1 (en) * | 2004-04-20 | 2007-01-10 | Sanofi-Aventis | Clopidogrel salt and polymorphic forms thereof |
| CN1997648A (zh) * | 2004-04-20 | 2007-07-11 | 赛诺菲-安万特 | (+)－(S)－α－(2－氯苯基)－6,7－二氢噻吩并[3,2－C]吡啶－5(4H)乙酸甲酯氢溴酸盐，即氯吡格雷氢溴酸盐的多晶型物 |
| US20050256314A1 (en) * | 2004-05-04 | 2005-11-17 | Soojin Kim | Process employing controlled crystallization in forming crystals of a pharmaceutical |
| US7829720B2 (en) | 2004-05-04 | 2010-11-09 | Bristol-Myers Squibb Company | Process for preparing atazanavir bisulfate and novel forms |
| US20050288343A1 (en) * | 2004-05-19 | 2005-12-29 | Andrew Rusowicz | Process of preparing substituted carbamates and intermediates thereof |
| TWI354569B (en) * | 2004-05-28 | 2011-12-21 | Bristol Myers Squibb Co | Coated tablet formulation and method |
| WO2005117866A1 (en) * | 2004-06-01 | 2005-12-15 | Ivax Pharmaceuticals S.R.O. | Amorphous clopidogrel hydrochloride and its antithrombotic use |
| JP2007513889A (ja) * | 2004-09-21 | 2007-05-31 | テバ ファーマシューティカル インダストリーズ リミティド | 結晶性クロピドグレル臭酸塩及びその調製方法 |
| US7446200B2 (en) * | 2004-10-04 | 2008-11-04 | Usv, Ltd. | Rapid resolution process of clopidogrel base and a process for preparation of clopidogrel bisulfate polymorph-form I |
| CZ20041048A3 (cs) * | 2004-10-18 | 2005-11-16 | Zentiva, A. S | Způsob výroby klopidogrelu |
| EP1674468A1 (en) * | 2004-12-21 | 2006-06-28 | Ratiopharm GmbH | Polymorphs of clopidogrel hydrobromide |
| AU2005327776A1 (en) * | 2005-02-15 | 2006-08-24 | Usv Limited | Rapid resolution process for clopidogrel base and a process for preparation of Clopidogrel bisulfate polymorph - Form I |
| MX2007010267A (es) * | 2005-02-24 | 2007-09-11 | Teva Pharma | Base de clopidogrel adecuada para formulacion farmaceutica y preparacion de ella. |
| CZ299213B6 (cs) | 2005-03-08 | 2008-05-21 | Zentiva, A. S | Zpusob racemizace R(-) izomeru methylesteru kyseliny (2-chlorfenyl)-6,7-dihydro-thieno[3,2-c]pyridin-5(4H)-octové |
| US7772398B2 (en) * | 2005-03-11 | 2010-08-10 | Dr. Reddy's Laboratories, Inc. | Process for making crystalline form I of clopidogrel hydrogen sulphate |
| BRPI0608771A2 (pt) * | 2005-05-10 | 2010-01-26 | Elan Pharma Int Ltd | formulações de clopidogrel em nanopartìcula |
| KR100678287B1 (ko) * | 2005-06-23 | 2007-02-02 | 한미약품 주식회사 | 클로피도그렐의 제조방법 및 이에 사용되는 중간체 |
| EP1902058A2 (en) * | 2005-07-12 | 2008-03-26 | RPG Life Sciences Limited | A process for preparation of methyl-(+)-(s)-alpha-(2-chlorophenyl)-6,7-dihydrothieno(3,2-c)pyridine-5(4h)-acetic acid methyl ester or salts thereof having higher chiral purity and products thereof |
| KR20070009851A (ko) * | 2005-07-14 | 2007-01-19 | 씨제이 주식회사 | 클로피도그렐 황산수소염 함유 약학 조성물 |
| WO2007052300A2 (en) | 2005-09-05 | 2007-05-10 | Cadila Healthcare Limited | Processes for the preparation of different forms of (s)-(+)-clopidogrel besylate |
| CN101253179B (zh) * | 2005-09-21 | 2010-12-29 | 株式会社钟根堂 | S-氯吡格雷的树脂酸盐复合物及其制备方法 |
| KR100783286B1 (ko) * | 2005-09-26 | 2007-12-06 | 주식회사종근당 | 클로피도그렐 우선성 광학이성체의 유리염기를 함유하는고형의 약제학적 조성물 |
| DE102005060690B4 (de) * | 2005-12-15 | 2008-09-25 | Capsulution Nanoscience Ag | Salze von Clopidogrel mit Polyanionen und ihre Verwendung zur Herstellung pharmazeutischer Formulierungen |
| KR101235117B1 (ko) * | 2005-12-26 | 2013-02-20 | 에스케이케미칼주식회사 | 광학분리에 의한 (ｓ)-(＋)-클로피도그렐의 제조방법 |
| KR20070094230A (ko) * | 2006-03-17 | 2007-09-20 | 한미약품 주식회사 | 클로피도그렐 캄파술폰산염 또는 이의 결정다형을 함유하는약학 조성물 |
| US20070225320A1 (en) * | 2006-03-27 | 2007-09-27 | Eswaraiah Sajja | Process for preparing clopidogrel |
| EP2007362B1 (en) | 2006-04-04 | 2018-09-05 | KG Acquisition LLC | Oral dosage forms including an antiplatelet agent and an acid inhibitor |
| WO2007125544A2 (en) * | 2006-04-27 | 2007-11-08 | Ind-Swift Laboratories Limited | Process for the preparation of polymorphic forms of clopidogrel hydrogen sulfate |
| KR20080055860A (ko) * | 2006-08-03 | 2008-06-19 | 테바 파마슈티컬 인더스트리즈 리미티드 | 클로피도그렐 바이설페이트의 제조 방법 |
| US8247558B2 (en) * | 2006-09-04 | 2012-08-21 | Ranbaxy Laboratories Limited | Process for the preparation of clopidogrel and its pharmaceutically acceptable salts |
| EP1900358A1 (en) * | 2006-09-16 | 2008-03-19 | Cimex Pharma AG | Pharmaceutical formulations comprising clopidogrel |
| SI22383A (sl) * | 2006-09-22 | 2008-04-30 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Nov postopek sinteze klopidogrela in nove oblike njegovih farmacevtsko sprejemljivih soli |
| KR100978498B1 (ko) * | 2006-10-17 | 2010-08-30 | 최중헌 | 클로피도그렐 황산수소염의 제조방법 |
| WO2008060934A2 (en) * | 2006-11-14 | 2008-05-22 | Acusphere, Inc. | Formulations of tetrahydropyridine antiplatelet agents for parenteral or oral administration |
| US20080194560A1 (en) * | 2006-12-22 | 2008-08-14 | Zhi Yun Wang | Disintegration promoters in solid dose wet granulation formulations |
| EP1970054A3 (en) | 2007-03-14 | 2009-06-03 | Ranbaxy Laboratories Limited | Clopidogrel tablets |
| PL382055A1 (pl) * | 2007-03-23 | 2008-09-29 | Koźluk Tomasz Nobilus Ent | Sposób wytwarzania formy krystalicznej 1 wodorosiarczanu klopidogrelu |
| EP1980563A1 (en) | 2007-04-09 | 2008-10-15 | BATTULA, Srinivasa Reddy | Procedure for the preparation of methyl (+)-(S)-Alpha-(O-chlorophenyl)-6,7-dihydrothieno-[3,2-C]pyridine-5(4H) acetate |
| BRPI0803101A2 (pt) * | 2007-04-18 | 2014-04-22 | Teva Pharma | Processos melhores para preparação de clopidogrel |
| RU2470636C2 (ru) * | 2007-04-27 | 2012-12-27 | Сайдекс Фамэсьютиклз, Инк. | Композиция клопидогреля и сульфоалкилового эфира циклодекстрина (варианты) и способы лечения заболеваний посредством названной композиции (варианты) |
| US20100297621A1 (en) * | 2007-06-20 | 2010-11-25 | University Of Utah Research Foundation | Use of pre-mrna splicing in platelet cells for the diagnosis of disease |
| DE602008005462D1 (de) * | 2007-06-22 | 2011-04-21 | Bristol Myers Squibb Co | Tablettierte atazanavirhaltige zusammensetzungen |
| PL2178513T3 (pl) * | 2007-06-22 | 2011-09-30 | Bristol Myers Squibb Holdings Ireland | Kompozycje w tabletkach zawierające atazanawir |
| KR101686243B1 (ko) * | 2007-06-22 | 2016-12-13 | 브리스톨-마이어스 스퀴브 홀딩스 아일랜드 | 아타자나비르를 함유하는 정제 조성물 |
| AU2008268627A1 (en) * | 2007-06-22 | 2008-12-31 | Bristol-Myers Squibb Company | Tableted compositions containing atazanavir |
| KR20090022616A (ko) * | 2007-08-31 | 2009-03-04 | 한올제약주식회사 | 베실산클로피도그렐 함유 경구투여용 약제 |
| JP2011506950A (ja) * | 2007-12-14 | 2011-03-03 | ジェネリクス・（ユーケー）・リミテッド | クロピドグレルを分析するためのｈｐｌｃ法 |
| WO2009080469A1 (en) * | 2007-12-24 | 2009-07-02 | Sandoz Ag | Process for the preparation of clopidogrel bisulphate form i |
| ATE530172T1 (de) * | 2008-02-26 | 2011-11-15 | Lesvi Laboratorios Sl | Pharmazeutische formulierungen mit clopidogrel |
| WO2009123210A1 (ja) | 2008-04-01 | 2009-10-08 | アステラス製薬株式会社 | 血管性疾患の予防剤及び／又は治療剤 |
| EP2107061A1 (en) | 2008-04-02 | 2009-10-07 | Krka Tovarna Zdravil, D.D., Novo Mesto | Process for the preparation of optically enriched clopidogrel |
| US20090264460A1 (en) * | 2008-04-21 | 2009-10-22 | Mamta Mishra | Clopidogrel pharmaceutical formulations |
| KR100990949B1 (ko) | 2008-06-09 | 2010-10-29 | 엔자이텍 주식회사 | 클로피도그렐 및 그의 유도체의 제조방법 |
| US8299097B2 (en) * | 2008-09-12 | 2012-10-30 | The Brigham And Women's Hospital, Inc. | Methods for treating inflammatory disorders |
| US20110190502A1 (en) * | 2008-10-24 | 2011-08-04 | Sandoz Ag | Process for the preparation of s-clopidogrel |
| DE202010018378U1 (de) | 2009-04-10 | 2016-04-07 | Tufts Medical Center, Inc. | PAR-1-Aktivierung durch Metalloproteinase-1 (MMP-1) |
| CN101885730B (zh) * | 2009-05-13 | 2012-07-04 | 连云港恒邦医药科技有限公司 | 抗血栓的化合物 |
| PT3100728T (pt) | 2009-05-13 | 2020-02-21 | Cydex Pharmaceuticals Inc | Composições farmacêuticas que compreendem prasugrel e derivados da ciclodextrina e métodos de produção e utilização dos mesmos |
| JP2012529431A (ja) | 2009-06-08 | 2012-11-22 | メルク・シャープ・アンド・ドーム・コーポレーション | トロンビン受容体アンタゴニストおよびクロピドグレルの固定用量錠剤 |
| EA021588B1 (ru) | 2009-06-25 | 2015-07-30 | Тетра Сиа | Бетаиновые соли ацетилсалициловой кислоты |
| WO2011009020A2 (en) | 2009-07-16 | 2011-01-20 | Mallinckrodt Inc. | Compounds and compositions for use in phototherapy and in treatment of ocular neovascular disease and cancers |
| WO2011010318A1 (en) * | 2009-07-23 | 2011-01-27 | Praveen Laboratories Private Limited | Process for the preparation of clopidogrel polymorphous form 1 using seed chrystals |
| WO2011042804A2 (en) | 2009-10-08 | 2011-04-14 | Jubliant Life Sciences Limited | An improved process for the preparation of clopidogrel hydrogen sulfate form i |
| WO2011051976A2 (en) | 2009-10-30 | 2011-05-05 | Matrix Laboratories Ltd | An improved process for the preparation of clopidogrel bisulfate form i |
| CN102863457B (zh) | 2010-02-02 | 2013-10-09 | 江苏威凯尔医药科技有限公司 | 光学活性2-羟基四氢噻吩并吡啶衍生物及其制备方法与在制药中的用途 |
| CN101766573B (zh) | 2010-02-05 | 2013-02-13 | 上海安必生制药技术有限公司 | 硫酸氢氯吡格雷固体制剂的制备工艺 |
| WO2011101865A2 (en) | 2010-02-19 | 2011-08-25 | Cadila Healthcare Limited | Stable pharmaceutical compositions of clopidogrel for parenteral delivery |
| CN101787033B (zh) * | 2010-03-16 | 2011-08-31 | 天津市中央药业有限公司 | 一种硫酸氢氯吡格雷有关物质c的合成方法 |
| WO2011125069A1 (en) | 2010-03-22 | 2011-10-13 | Rpg Life Sciences Limited | A process for preparation of crystalline form i of clopidogrel bisulfate |
| WO2011132201A1 (en) | 2010-04-19 | 2011-10-27 | Cadila Healthcare Limited | A pharmaceutical composition comprising antiplatelet agents and an erythropoiesis stimulating agent |
| CN101863902B (zh) * | 2010-06-29 | 2012-06-27 | 天津药物研究院 | 2-取代苯基-2-(4,5,6,7-四氢噻吩并[3,2-c]吡啶-5（4H）-基)乙酸(取代烷基醇)酯的制备方法和用途 |
| WO2012007019A1 (en) | 2010-07-13 | 2012-01-19 | Pharmathen S.A. | Process for the preparation of clopidogrel and salts thereof |
| WO2012123958A1 (en) | 2011-02-14 | 2012-09-20 | Cadila Healthcare Limited | Highly pure salts of clopidogrel free of genotoxic impurities |
| CN102199160B (zh) * | 2011-03-22 | 2016-06-22 | 浙江华海药业股份有限公司 | 一种制备ⅰ型硫酸氢氯吡格雷的方法 |
| CA2839608C (en) | 2011-06-27 | 2020-07-14 | Ipca Laboratories Limited | (7as,2's)-2-oxoclopidogrel as anti-thrombotic compounds |
| CN104114163A (zh) | 2011-12-09 | 2014-10-22 | 沃克哈特有限公司 | 治疗心血管疾病的方法 |
| CN103665042B (zh) * | 2012-09-21 | 2016-03-16 | 北京普禄德医药科技有限公司 | 光学活性的2-羟基四氢噻吩并吡啶衍生物及其制备方法和用途 |
| WO2014118802A1 (en) | 2013-01-31 | 2014-08-07 | Pharmazell Gmbh | An improved process for the preparation of clopidogrel bisulfate form-i |
| CN104761567A (zh) * | 2014-01-02 | 2015-07-08 | 上海医药工业研究院 | 一种硫酸氢氯吡格雷、其中间体及制备方法 |
| DE102014108210A1 (de) | 2014-06-11 | 2015-12-17 | Dietrich Gulba | Rodentizid |
| HUP1400294A2 (hu) | 2014-06-13 | 2015-12-28 | Skillpharm Kft | Clopidogrel új alkalmazása |
| KR101710922B1 (ko) | 2015-06-03 | 2017-02-28 | 경동제약 주식회사 | 클로피도그렐 황산염 결정형 i형의 제조방법 |
| CN107698620A (zh) | 2015-06-23 | 2018-02-16 | 江苏天士力帝益药业有限公司 | 一种氘代噻吩并哌啶衍生物、制备方法及其应用 |
| EP3646865A4 (en) | 2017-06-30 | 2021-03-17 | Kowa Company, Ltd. | MEDICINE |
| CN110627808B (zh) * | 2018-06-21 | 2022-04-01 | 江苏同禾药业有限公司 | 一种硫酸氢氯吡格雷拆分母液的回收处理工艺 |
| EP4070658A1 (de) | 2021-04-06 | 2022-10-12 | BIORoxx GmbH | Verwendung von blutgerinnungshemmenden verbindungen als rodentizide |
| WO2023012479A1 (en) | 2021-08-03 | 2023-02-09 | Liqmeds Worldwide Limited | An oral pharmaceutical solution of clopidogrel |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2530247B1 (fr) * | 1982-07-13 | 1986-05-16 | Sanofi Sa | Nouveaux derives de la thieno (3, 2-c) pyridine, leur procede de preparation et leur application therapeutique |
| DE3621413A1 (de) * | 1986-06-26 | 1988-01-07 | Boehringer Ingelheim Kg | Verwendung carbocyclisch und heterocyclisch annelierter dihydropyridine als cardioprotektive mittel sowie neue heterocyclisch und carbocyclisch anellierte dihydropyridine, verfahren zu deren herstellung und zwischenstufen fuer deren herstellung |
| DE3736664A1 (de) * | 1987-10-29 | 1989-05-11 | Boehringer Ingelheim Kg | Tetrahydro-furo- und -thieno(2,3-c)pyridine, ihre verwendung als arzneimittel und verfahren zu ihrer herstellung |
-
1987
- 1987-11-27 FR FR878716516A patent/FR2623810B2/fr not_active Expired - Lifetime
-
1988
- 1988-02-01 IE IE27388A patent/IE66922B1/en active Protection Beyond IP Right Term
- 1988-02-02 IL IL85294A patent/IL85294A/xx not_active IP Right Cessation
- 1988-02-04 AU AU11292/88A patent/AU597784B2/en not_active Revoked
- 1988-02-05 YU YU23188A patent/YU46748B/sh unknown
- 1988-02-05 SI SI8810231A patent/SI8810231A8/sl unknown
- 1988-02-08 MY MYPI88000121A patent/MY103198A/en unknown
- 1988-02-08 CA CA000558412A patent/CA1336777C/en not_active Expired - Lifetime
- 1988-02-09 PT PT86726A patent/PT86726B/pt not_active IP Right Cessation
- 1988-02-10 NZ NZ223475A patent/NZ223475A/xx unknown
- 1988-02-11 PH PH36488A patent/PH25960A/en unknown
- 1988-02-12 US US07/155,550 patent/US4847265A/en not_active Expired - Lifetime
- 1988-02-15 TN TNTNSN88012A patent/TNSN88012A1/fr unknown
- 1988-02-15 MA MA21421A patent/MA21184A1/fr unknown
- 1988-02-16 DE DE1998175053 patent/DE19875053I2/de active Active
- 1988-02-16 EP EP88400346A patent/EP0281459B1/fr not_active Expired - Lifetime
- 1988-02-16 KR KR1019880001714A patent/KR960003615B1/ko not_active IP Right Cessation
- 1988-02-16 AT AT88400346T patent/ATE121745T1/de active
- 1988-02-16 FI FI880720A patent/FI87216C/fi active Protection Beyond IP Right Term
- 1988-02-16 HU HU88747A patent/HU197909B/hu unknown
- 1988-02-16 NO NO880666A patent/NO165924C/no not_active IP Right Cessation
- 1988-02-16 AR AR88310091A patent/AR243891A1/es active
- 1988-02-16 CS CS96588A patent/CS274420B2/cs not_active IP Right Cessation
- 1988-02-16 ES ES88400346T patent/ES2071621T4/es not_active Expired - Lifetime
- 1988-02-16 RO RO132221A patent/RO99191B1/ro unknown
- 1988-02-16 JP JP63034943A patent/JPH0645622B2/ja not_active Expired - Lifetime
- 1988-02-16 PL PL1988270677A patent/PL156689B1/pl unknown
- 1988-02-16 DE DE3853643T patent/DE3853643T2/de not_active Expired - Lifetime
- 1988-02-16 DK DK198800800A patent/DK173636B1/da not_active IP Right Cessation
- 1988-02-16 OA OA59285A patent/OA08808A/xx unknown
-
1992
- 1992-06-19 MX MX9203026A patent/MX9203026A/es unknown
- 1992-10-02 HR HR920923A patent/HRP920923B1/xx not_active IP Right Cessation
-
1995
- 1995-02-01 HU HU95P/P00071P patent/HU210538A9/hu unknown
-
1996
- 1996-07-18 LV LV960270A patent/LV5804B4/xx unknown
-
1997
- 1997-07-08 HK HK97101520A patent/HK1000093A1/xx not_active IP Right Cessation
-
1998
- 1998-04-13 CY CY9800003A patent/CY2087B1/xx unknown
- 1998-11-27 LU LU90324C patent/LU90324I2/xx unknown
-
1999
- 1999-01-07 NL NL990002C patent/NL990002I1/nl unknown
- 1999-10-11 NO NO1999022C patent/NO1999022I1/no unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PH25960A (en) | Dextro-rotatory enantiomer of methyl alpha-5-(4,5-6,7-tetrahydro (3,2-C) thieno pyridyl (2-chloro-phenyl) acetate and the pharmaceutical compositions containing it | |
| TWI290927B (en) | 2-Acetoxy-5-(alpha-cyclopropylcarbonyl-2-fluorobenzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine acid-additive salts | |
| CA2839608C (en) | (7as,2's)-2-oxoclopidogrel as anti-thrombotic compounds | |
| EP2613783B1 (en) | Methods for the treatment or prophylaxis of thrombosis or embolism | |
| NO159725B (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive tieno (3,2-c)pyridinderivater. | |
| IE862805L (en) | Benzimidazole derivatives | |
| EP0018104B1 (en) | Tetrahydroisoquinolines, their production and the compounds and pharmaceutical compositions containing them for use in the prevention or treatment of hypertension | |
| EP0161422B1 (en) | Alkanolamine derivatives and platelet aggregation inhibitors containing the same as an active ingredient | |
| AU628995B2 (en) | Novel thienopyran derivatives, a process for their preparation and their use | |
| IE55458B1 (en) | New thieno-pyridinone derivative,process for its preparation,and therapeutic applications thereof | |
| JPH0575728B2 (ja) | ||
| JPS6144870A (ja) | 不飽和脂肪酸アミド誘導体およびこれを含有する血小板凝集抑制剤 | |
| SK34893A3 (en) | Indenindole derivatives, process for their preparation and their pharmaceutical compositions | |
| CN112778371B (zh) | 一种噻吩并吡啶衍生物及其制备方法和用途 | |
| HU185069B (en) | Process for producing 5,6,7,7a-tetrahydro-4h-thieno-bracket-3,2-c-bracket closed-pyridin-2-one-derivatives | |
| FI88039C (fi) | Foerfarande foer framstaellning av 2,3-dihydro-1-(8-metyl-1,2,4-triatsolo/4,3-b/pyridazin-6-yl)-4(1h)-pyridinon | |
| DD272085A5 (de) | Verfahren zur herstellung des rechtsdrehenden isomeren von alpha-(4,5,6,7-tetrahydro-(3,2-c)-thieno-5-pyridyl)-(2-chlor-phenyl)-essigsaeure--methylester | |
| JPS6287570A (ja) | ピリジン誘導体およびこれを含有するトロンボキサンａ↓２合成酵素阻害剤 | |
| JPH01128971A (ja) | ピラジン誘導体およびこれを含有する血小板凝集抑制剤 | |
| HU189012B (en) | Process for production of optically active 3-ethil-2,6-dimethil-6,7,8,9-tetrahydro-4h-pirido /1,2-a/-piramidin-4-on enentiomers |