IL96811A - Transformed history of oxazole thiazole oxadiazole and thiaziazole preparation and pharmaceutical preparations containing them - Google Patents

Transformed history of oxazole thiazole oxadiazole and thiaziazole preparation and pharmaceutical preparations containing them

Info

Publication number: IL96811A
Authority: IL; Israel
Prior art keywords: formula; pyridyl; alkyl; halogen; compounds
Prior art date: 1989-12-29

Application number

IL9681190A

Other languages

English (en)

Hebrew (he)

Other versions

IL96811A0 (en

Original Assignee

Sanofi Sa

Priority date (The priority date 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 date listed.)

1989-12-29

Filing date

1990-12-27

Publication date

1995-03-15

1990-12-27 Application filed by Sanofi Sa filed Critical Sanofi Sa

1991-09-16 Publication of IL96811A0 publication Critical patent/IL96811A0/xx

1995-03-15 Publication of IL96811A publication Critical patent/IL96811A/en

Links

238000002360 preparation method Methods 0.000 title claims description 14
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical class C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 title claims description 10
239000008194 pharmaceutical composition Substances 0.000 title claims description 5
WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical class C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 title description 2
150000002916 oxazoles Chemical class 0.000 title description 2
OIWIYLWZIIJNHU-UHFFFAOYSA-N 1-sulfanylpyrazole Chemical class SN1C=CC=N1 OIWIYLWZIIJNHU-UHFFFAOYSA-N 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 99
150000003839 salts Chemical class 0.000 claims abstract description 89
-1 CONQ1Q2 or CSNQ1Q2 Chemical group 0.000 claims abstract description 45
229910052736 halogen Inorganic materials 0.000 claims abstract description 29
150000002367 halogens Chemical class 0.000 claims abstract description 29
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 18
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 12
229910052717 sulfur Inorganic materials 0.000 claims abstract description 12
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 11
125000002947 alkylene group Chemical group 0.000 claims abstract description 9
229910052799 carbon Inorganic materials 0.000 claims abstract description 7
125000001041 indolyl group Chemical group 0.000 claims abstract description 7
125000004076 pyridyl group Chemical group 0.000 claims abstract description 7
125000005956 isoquinolyl group Chemical group 0.000 claims abstract description 5
125000000714 pyrimidinyl group Chemical group 0.000 claims abstract description 5
125000005493 quinolyl group Chemical group 0.000 claims abstract description 5
125000005309 thioalkoxy group Chemical group 0.000 claims abstract description 5
125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims abstract description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 3
125000002541 furyl group Chemical group 0.000 claims abstract 2
125000001624 naphthyl group Chemical group 0.000 claims abstract 2
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract 2
238000000034 method Methods 0.000 claims description 47
150000001412 amines Chemical class 0.000 claims description 45
238000006243 chemical reaction Methods 0.000 claims description 42
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 42
125000000217 alkyl group Chemical group 0.000 claims description 31
125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 30
230000008569 process Effects 0.000 claims description 22
229910052739 hydrogen Inorganic materials 0.000 claims description 18
239000002253 acid Substances 0.000 claims description 14
125000003545 alkoxy group Chemical group 0.000 claims description 11
125000003277 amino group Chemical group 0.000 claims description 11
239000001257 hydrogen Substances 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 7
150000003141 primary amines Chemical class 0.000 claims description 6
238000006467 substitution reaction Methods 0.000 claims description 6
HVAUUPRFYPCOCA-AREMUKBSSA-N 2-O-acetyl-1-O-hexadecyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCOC[C@@H](OC(C)=O)COP([O-])(=O)OCC[N+](C)(C)C HVAUUPRFYPCOCA-AREMUKBSSA-N 0.000 claims description 5
108010003541 Platelet Activating Factor Proteins 0.000 claims description 5
150000007513 acids Chemical class 0.000 claims description 5
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical group [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 5
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 5
IDNVUFHBLUELPI-UHFFFAOYSA-N 4-(2,4,6-trimethylphenyl)-1,3-thiazole Chemical compound CC1=CC(C)=CC(C)=C1C1=CSC=N1 IDNVUFHBLUELPI-UHFFFAOYSA-N 0.000 claims description 4
238000009833 condensation Methods 0.000 claims description 4
230000005494 condensation Effects 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
150000001721 carbon Chemical group 0.000 claims description 3
201000010099 disease Diseases 0.000 claims description 3
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
FWXZIERAYNWRDA-UHFFFAOYSA-N thiocyanatocarbonyl thiocyanate Chemical compound N#CSC(=O)SC#N FWXZIERAYNWRDA-UHFFFAOYSA-N 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
FWQALAORFNSAID-UHFFFAOYSA-N CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=C(Br)SC=N1 Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=C(Br)SC=N1 FWQALAORFNSAID-UHFFFAOYSA-N 0.000 claims description 2
PGJRGPIJHATNAK-UHFFFAOYSA-N CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=C(Cl)SC=N1 Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=C(Cl)SC=N1 PGJRGPIJHATNAK-UHFFFAOYSA-N 0.000 claims description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
230000026030 halogenation Effects 0.000 claims description 2
238000005658 halogenation reaction Methods 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims description 2
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
QGBWQVFTHMXFHF-UHFFFAOYSA-N 4-(2,4-dichlorophenyl)-5-methyl-1,3-thiazole Chemical compound S1C=NC(C=2C(=CC(Cl)=CC=2)Cl)=C1C QGBWQVFTHMXFHF-UHFFFAOYSA-N 0.000 claims 1
ZYMHCFYHVYGFMS-UHFFFAOYSA-N 5-methyl-1,3-oxazole Chemical compound CC1=CN=CO1 ZYMHCFYHVYGFMS-UHFFFAOYSA-N 0.000 claims 1
125000005518 carboxamido group Chemical group 0.000 claims 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
125000004434 sulfur atom Chemical group 0.000 claims 1
101000860842 Homo sapiens Ubiquinone biosynthesis O-methyltransferase, mitochondrial Proteins 0.000 abstract description 2
102100028229 Ubiquinone biosynthesis O-methyltransferase, mitochondrial Human genes 0.000 abstract description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
125000002883 imidazolyl group Chemical group 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
125000001544 thienyl group Chemical group 0.000 abstract 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 136
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 87
239000000203 mixture Substances 0.000 description 66
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 57
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 48
239000000243 solution Substances 0.000 description 45
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 43
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 42
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 42
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 36
239000000155 melt Substances 0.000 description 35
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 34
239000007864 aqueous solution Substances 0.000 description 31
239000000047 product Substances 0.000 description 31
239000002904 solvent Substances 0.000 description 30
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 28
239000012074 organic phase Substances 0.000 description 28
239000000377 silicon dioxide Substances 0.000 description 21
238000001990 intravenous administration Methods 0.000 description 20
229940093499 ethyl acetate Drugs 0.000 description 19
235000019439 ethyl acetate Nutrition 0.000 description 19
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 18
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 16
101150117004 atg18 gene Proteins 0.000 description 15
150000002576 ketones Chemical class 0.000 description 15
239000008346 aqueous phase Substances 0.000 description 14
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
238000004587 chromatography analysis Methods 0.000 description 12
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 12
238000010992 reflux Methods 0.000 description 12
239000002244 precipitate Substances 0.000 description 11
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 10
238000004821 distillation Methods 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 9
239000011541 reaction mixture Substances 0.000 description 9
WEGYGNROSJDEIW-UHFFFAOYSA-N 3-Acetylpyridine Chemical compound CC(=O)C1=CC=CN=C1 WEGYGNROSJDEIW-UHFFFAOYSA-N 0.000 description 8
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 8
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 8
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 7
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
229910052794 bromium Inorganic materials 0.000 description 7
239000000284 extract Substances 0.000 description 7
239000000706 filtrate Substances 0.000 description 7
238000002844 melting Methods 0.000 description 7
230000008018 melting Effects 0.000 description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(ii) bromide Chemical compound [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 description 6
239000007787 solid Substances 0.000 description 6
ARTCTEGBKRPORJ-UHFFFAOYSA-N 4-[2,4,6-tri(propan-2-yl)phenyl]-1,3-thiazole Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CSC=N1 ARTCTEGBKRPORJ-UHFFFAOYSA-N 0.000 description 5
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 5
230000002378 acidificating effect Effects 0.000 description 5
239000005557 antagonist Substances 0.000 description 5
239000000543 intermediate Substances 0.000 description 5
235000006408 oxalic acid Nutrition 0.000 description 5
150000003335 secondary amines Chemical class 0.000 description 5
229910000033 sodium borohydride Inorganic materials 0.000 description 5
239000012279 sodium borohydride Substances 0.000 description 5
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
101150041968 CDC13 gene Proteins 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 4
LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 4
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
239000012467 final product Substances 0.000 description 4
150000002391 heterocyclic compounds Chemical class 0.000 description 4
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
229910000041 hydrogen chloride Inorganic materials 0.000 description 4
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
235000017557 sodium bicarbonate Nutrition 0.000 description 4
239000000126 substance Substances 0.000 description 4
150000003585 thioureas Chemical class 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
BNWVZLQRZAFJFW-UHFFFAOYSA-N 3-(2,4,6-trimethylphenyl)-1,2,4-thiadiazole Chemical compound CC1=CC(C)=CC(C)=C1C1=NSC=N1 BNWVZLQRZAFJFW-UHFFFAOYSA-N 0.000 description 3
JJBDWBUEPCGFMN-UHFFFAOYSA-N 3-phenyl-1,2,4-oxadiazole Chemical compound O1C=NC(C=2C=CC=CC=2)=N1 JJBDWBUEPCGFMN-UHFFFAOYSA-N 0.000 description 3
CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
208000009079 Bronchial Spasm Diseases 0.000 description 3
208000014181 Bronchial disease Diseases 0.000 description 3
206010006482 Bronchospasm Diseases 0.000 description 3
229910021590 Copper(II) bromide Inorganic materials 0.000 description 3
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
150000001204 N-oxides Chemical class 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 3
239000012346 acetyl chloride Substances 0.000 description 3
230000002776 aggregation Effects 0.000 description 3
238000004220 aggregation Methods 0.000 description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
229910021529 ammonia Inorganic materials 0.000 description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
125000004744 butyloxycarbonyl group Chemical group 0.000 description 3
150000004657 carbamic acid derivatives Chemical class 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000001914 filtration Methods 0.000 description 3
229910000042 hydrogen bromide Inorganic materials 0.000 description 3
238000002347 injection Methods 0.000 description 3
239000007924 injection Substances 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
239000002808 molecular sieve Substances 0.000 description 3
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
QJZUKDFHGGYHMC-UHFFFAOYSA-N pyridine-3-carbaldehyde Chemical compound O=CC1=CC=CN=C1 QJZUKDFHGGYHMC-UHFFFAOYSA-N 0.000 description 3
238000012552 review Methods 0.000 description 3
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
238000003756 stirring Methods 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical class NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 description 2
YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
HPBPNWPROCLLAA-UHFFFAOYSA-N 2-bromoethanone Chemical compound BrC[C]=O HPBPNWPROCLLAA-UHFFFAOYSA-N 0.000 description 2
KQQVDTXEMQHUDG-UHFFFAOYSA-N 2-chloro-4-(2,4-dichlorophenyl)-5-methyl-1,3-oxazole Chemical compound O1C(Cl)=NC(C=2C(=CC(Cl)=CC=2)Cl)=C1C KQQVDTXEMQHUDG-UHFFFAOYSA-N 0.000 description 2
QQVNJGSZBSTGBJ-UHFFFAOYSA-N 2-oxoethyl thiocyanate Chemical compound O=CCSC#N QQVNJGSZBSTGBJ-UHFFFAOYSA-N 0.000 description 2
LUVQCMCOZJXCQO-UHFFFAOYSA-N 4-(2,4-dichlorophenyl)-5-methyl-1,3-oxazole Chemical compound O1C=NC(C=2C(=CC(Cl)=CC=2)Cl)=C1C LUVQCMCOZJXCQO-UHFFFAOYSA-N 0.000 description 2
PGALNNKTAOWXHY-UHFFFAOYSA-N 5-chloro-3-(2,4-dimethylphenyl)-1,2,4-oxadiazole Chemical compound CC1=CC(C)=CC=C1C1=NOC(Cl)=N1 PGALNNKTAOWXHY-UHFFFAOYSA-N 0.000 description 2
UPULOMQHYQDNNT-UHFFFAOYSA-N 5h-1,3-oxazol-2-one Chemical class O=C1OCC=N1 UPULOMQHYQDNNT-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
241000700199 Cavia porcellus Species 0.000 description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
238000005727 Friedel-Crafts reaction Methods 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
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JBJYTZXCZDNOJW-JLHYYAGUSA-N ic261 Chemical compound COC1=CC(OC)=CC(OC)=C1\C=C\1C2=CC=CC=C2NC/1=O JBJYTZXCZDNOJW-JLHYYAGUSA-N 0.000 description 1
150000002466 imines Chemical class 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
230000004968 inflammatory condition Effects 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
150000002540 isothiocyanates Chemical class 0.000 description 1
208000017169 kidney disease Diseases 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
239000003589 local anesthetic agent Substances 0.000 description 1
229960005015 local anesthetics Drugs 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
229910052987 metal hydride Inorganic materials 0.000 description 1
150000004681 metal hydrides Chemical class 0.000 description 1
QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
229940032007 methylethyl ketone Drugs 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
208000031225 myocardial ischemia Diseases 0.000 description 1
DILRJUIACXKSQE-UHFFFAOYSA-N n',n'-dimethylethane-1,2-diamine Chemical compound CN(C)CCN DILRJUIACXKSQE-UHFFFAOYSA-N 0.000 description 1
IFFWMMRYAJUJOW-UHFFFAOYSA-N n'-hydroxy-2,4-dimethylbenzenecarboximidamide Chemical compound CC1=CC=C(C(N)=NO)C(C)=C1 IFFWMMRYAJUJOW-UHFFFAOYSA-N 0.000 description 1
WQZXJTWTIYVJLT-UHFFFAOYSA-N n-ethylpiperidin-1-amine Chemical compound CCNN1CCCCC1 WQZXJTWTIYVJLT-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
238000010534 nucleophilic substitution reaction Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
ZDYUUBIMAGBMPY-UHFFFAOYSA-N oxalic acid;hydrate Chemical compound O.OC(=O)C(O)=O ZDYUUBIMAGBMPY-UHFFFAOYSA-N 0.000 description 1
RLXDCJUIXHSXQD-UHFFFAOYSA-N oxalic acid;hydrate Chemical compound O.OC(=O)C(O)=O.OC(=O)C(O)=O RLXDCJUIXHSXQD-UHFFFAOYSA-N 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 1
229950004354 phosphorylcholine Drugs 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
230000000770 proinflammatory effect Effects 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000000746 purification Methods 0.000 description 1
IDUGONKKOKQBPJ-UHFFFAOYSA-N pyridin-3-ylmethylthiourea Chemical compound NC(=S)NCC1=CC=CN=C1 IDUGONKKOKQBPJ-UHFFFAOYSA-N 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
210000002460 smooth muscle Anatomy 0.000 description 1
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
230000004936 stimulating effect Effects 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
230000016978 synaptic transmission, cholinergic Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 1
AZAGODUTIRCWRQ-UHFFFAOYSA-N tert-butyl n-(1-aminoethyl)carbamate Chemical compound CC(N)NC(=O)OC(C)(C)C AZAGODUTIRCWRQ-UHFFFAOYSA-N 0.000 description 1
KCOYXUILTLBUOI-UHFFFAOYSA-N tert-butyl n-[1-(pyridin-3-ylmethylamino)ethyl]carbamate Chemical compound CC(C)(C)OC(=O)NC(C)NCC1=CC=CN=C1 KCOYXUILTLBUOI-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
150000004867 thiadiazoles Chemical class 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
239000003071 vasodilator agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- 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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Bioinformatics & Cheminformatics (AREA)
Heart & Thoracic Surgery (AREA)
Cardiology (AREA)
Pulmonology (AREA)
Urology & Nephrology (AREA)
Epidemiology (AREA)
Hematology (AREA)
Vascular Medicine (AREA)
Immunology (AREA)
Pain & Pain Management (AREA)
Rheumatology (AREA)
Diabetes (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Thiazole And Isothizaole Compounds (AREA)
Indole Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

IL9681190A 1989-12-29 1990-12-27 Transformed history of oxazole thiazole oxadiazole and thiaziazole preparation and pharmaceutical preparations containing them IL96811A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR8917491A FR2656610B1 (fr)	1989-12-29	1989-12-29	Derives d'amino-2 phenyl-4 thiazole, leur procede de preparation et leur application therapeutique.

Publications (2)

Publication Number	Publication Date
IL96811A0 IL96811A0 (en)	1991-09-16
IL96811A true IL96811A (en)	1995-03-15

Family

ID=9389177

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9681190A IL96811A (en)	1989-12-29	1990-12-27	Transformed history of oxazole thiazole oxadiazole and thiaziazole preparation and pharmaceutical preparations containing them

Country Status (30)

Country	Link
US (5)	US5470855A (de)
EP (1)	EP0462264B1 (de)
JP (1)	JP2758077B2 (de)
KR (1)	KR0159517B1 (de)
CN (1)	CN1028757C (de)
AT (1)	ATE119160T1 (de)
AU (1)	AU627103B2 (de)
BR (1)	BR1100202A (de)
CA (1)	CA2046883C (de)
CZ (1)	CZ280803B6 (de)
DE (1)	DE69017443T2 (de)
DK (1)	DK0462264T3 (de)
ES (1)	ES2069276T3 (de)
FI (1)	FI95380C (de)
FR (1)	FR2656610B1 (de)
HU (2)	HUT61761A (de)
IE (1)	IE67322B1 (de)
IL (1)	IL96811A (de)
LV (1)	LV5803B4 (de)
MX (1)	MX9203019A (de)
NO (1)	NO179975C (de)
NZ (1)	NZ236678A (de)
PL (1)	PL167101B1 (de)
PT (1)	PT96368B (de)
RU (1)	RU2049784C1 (de)
SK (1)	SK627790A3 (de)
TW (1)	TW215921B (de)
UA (1)	UA35546C2 (de)
WO (1)	WO1991009857A1 (de)
ZA (1)	ZA9010447B (de)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9127304D0 (en) *	1991-12-23	1992-02-19	Boots Co Plc	Therapeutic agents
FR2692893B1 (fr) *	1992-06-24	1994-09-02	Sanofi Elf	Dérivés alkylamino ramifiés du thiazole, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent.
GB9312893D0 (en) *	1993-06-22	1993-08-04	Boots Co Plc	Therapeutic agents
FR2714059B1 (fr) *	1993-12-21	1996-03-08	Sanofi Elf	Dérivés amino ramifiés du thiazole, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent.
FR2728901B1 (fr) *	1994-12-28	1997-03-28	Sanofi Sa	Derives de phenyl-4-thiazoles substitues, procede pour leur preparation et compositions pharmaceutiques les contenant
US5795905A (en) *	1995-06-06	1998-08-18	Neurocrine Biosciences, Inc.	CRF receptor antagonists and methods relating thereto
FR2735777B1 (fr) *	1995-06-21	1997-09-12	Sanofi Sa	Derives de 4-phenylaminothiazole, leur procede de preparation et les compositions pharmaceutiques les contenant
NZ331104A (en) *	1995-12-29	2000-03-27	Boehringer Ingelheim Ca Ltd	Phenyl thiazole derivatives that inhibit herpes replication by inhibiting the herpes helicase primase enzyme complex
US6288091B1 (en)	1995-12-29	2001-09-11	Boehringer Ingelheim Ltd.	Antiherpes virus compounds and methods for their preparation and use
ZA9756B (en) *	1996-01-16	1997-07-17	Warner Lambert Co	Process for preparing 4,6-disubstituted pyrido[3,4-d]-pyrimidines
WO1997041097A2 (en) *	1996-12-31	1997-11-06	Dr. Reddy's Research Foundation	Novel heterocyclic compounds process for their preparation and pharmaceutical compositions containing them and their use in the treatment of diabetes and related diseases
FR2754258B1 (fr)	1996-10-08	1998-12-31	Sanofi Sa	Derives d'aminothiazole, leur procede de preparation et les compositions pharmaceutiques les contenant
ID23443A (id) *	1997-06-24	2000-04-20	Janssen Pharmaceutica Nv	Turunan tiadiazolil piridazin penghambat angiogenesis
US6057340A (en) *	1998-02-03	2000-05-02	American Home Products Corporation	Oxazole derivatives as serotonin-1A receptor agonists
FR2776925B3 (fr) *	1998-04-07	2000-05-26	Sanofi Sa	Utilisation de derives d'aminothiazole pour la preparation de medicaments pour le traitement des maladies entrainant une demyelinisation
UA75569C2 (en) *	1998-12-01	2006-05-15	Reddys Lab Ltd Dr	Pharmaceutical composition of thiadiazolidinedione and method for its manufacture
US6242448B1 (en)	1998-12-17	2001-06-05	American Home Products Corporation	Trisubstituted-oxazole derivatives as serotonin ligands
US6417360B1 (en) *	1999-03-03	2002-07-09	Hoffmann-La Roche Inc.	Heterocyclic sulfonamides
AR035016A1 (es) *	1999-08-25	2004-04-14	Takeda Chemical Industries Ltd	Composicion de azol promotor de produccion/secrecion de neurotrofina, compuesto prodroga del mismo, composicion farmaceutica que lo comprende y uso del mismo para preparar esta ultima.
ATE312606T1 (de) *	1999-10-29	2005-12-15	Orion Corp	Verwendung eines imidazolderivats zur behandlung oder verhütung von hypotension und schock
US6699866B2 (en)	2001-04-17	2004-03-02	Sepracor Inc.	Thiazole and other heterocyclic ligands for mammalian dopamine, muscarinic and serotonin receptors and transporters, and methods of use thereof
US6670071B2 (en) *	2002-01-15	2003-12-30	Quallion Llc	Electric storage battery construction and method of manufacture
NZ550114A (en) *	2004-04-20	2011-02-25	Transtech Pharma Inc	Substituted thiazole and pyrimidine derivatives as melanocortin receptor modulators
CN101573357B (zh)	2006-10-19	2013-01-23	武田药品工业株式会社	吲哚化合物
KR20100017372A (ko) *	2007-05-25	2010-02-16	애보트 게엠베하 운트 콤파니 카게	향대사성 글루타메이트 수용체 2（ｍｇｌｕ2 수용체）의 포지티브 조절자로서의 헤테로사이클릭 화합물
WO2010025142A1 (en) *	2008-08-29	2010-03-04	Transtech Pharma, Inc.	Substituted aminothiazole derivatives, pharmaceutical compositions, and methods of use
KR20240046893A (ko) *	2021-08-10	2024-04-11	텍사스 하트 인스티튜트	아미노아릴-인테그린 작용제 화합물

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE471555A (de) *	1943-06-22
EP0149884B1 (de) *	1983-09-09	1992-12-16	Takeda Chemical Industries, Ltd.	5-Pyridyl-1,3-Thiazol-Derivate, ihre Herstellung und Anwendung
FR2612187B1 (fr) *	1987-03-12	1989-07-21	Sanofi Sa	Derives du thiazole actifs sur le systeme cholinergique, leur procede de preparation et compositions pharmaceutiques en contenant

1989
- 1989-12-29 FR FR8917491A patent/FR2656610B1/fr not_active Expired - Fee Related
1990
- 1990-12-14 CZ CS906277A patent/CZ280803B6/cs not_active IP Right Cessation
- 1990-12-14 SK SK6277-90A patent/SK627790A3/sk unknown
- 1990-12-26 TW TW079110854A patent/TW215921B/zh active
- 1990-12-27 IL IL9681190A patent/IL96811A/en not_active IP Right Cessation
- 1990-12-27 PT PT96368A patent/PT96368B/pt not_active IP Right Cessation
- 1990-12-28 HU HU912819A patent/HUT61761A/hu unknown
- 1990-12-28 AU AU70555/91A patent/AU627103B2/en not_active Ceased
- 1990-12-28 ES ES91902715T patent/ES2069276T3/es not_active Expired - Lifetime
- 1990-12-28 HU HU912819A patent/HU213230B/hu not_active IP Right Cessation
- 1990-12-28 AT AT91902715T patent/ATE119160T1/de not_active IP Right Cessation
- 1990-12-28 KR KR1019910701025A patent/KR0159517B1/ko not_active Expired - Fee Related
- 1990-12-28 PL PL90292008A patent/PL167101B1/pl not_active IP Right Cessation
- 1990-12-28 CA CA002046883A patent/CA2046883C/en not_active Expired - Fee Related
- 1990-12-28 JP JP3502549A patent/JP2758077B2/ja not_active Expired - Fee Related
- 1990-12-28 WO PCT/FR1990/000970 patent/WO1991009857A1/fr not_active Ceased
- 1990-12-28 UA UA5001534A patent/UA35546C2/uk unknown
- 1990-12-28 DK DK91902715.1T patent/DK0462264T3/da active
- 1990-12-28 EP EP91902715A patent/EP0462264B1/de not_active Expired - Lifetime
- 1990-12-28 RU SU5001534/04A patent/RU2049784C1/ru not_active IP Right Cessation
- 1990-12-28 IE IE472190A patent/IE67322B1/en not_active IP Right Cessation
- 1990-12-28 ZA ZA9010447A patent/ZA9010447B/xx unknown
- 1990-12-28 DE DE69017443T patent/DE69017443T2/de not_active Expired - Fee Related
- 1990-12-29 CN CN90110167A patent/CN1028757C/zh not_active Expired - Fee Related
1991
- 1991-01-04 NZ NZ236678A patent/NZ236678A/en unknown
- 1991-08-28 FI FI914058A patent/FI95380C/fi active
- 1991-08-28 NO NO913378A patent/NO179975C/no unknown
1992
- 1992-06-19 MX MX9203019A patent/MX9203019A/es unknown
1993
- 1993-08-25 US US08/111,732 patent/US5470855A/en not_active Expired - Lifetime
1995
- 1995-08-04 US US08/511,468 patent/US5780468A/en not_active Expired - Fee Related
1996
- 1996-07-18 LV LV960269A patent/LV5803B4/xx unknown
1997
- 1997-04-01 BR BR1100202-6A patent/BR1100202A/pt active IP Right Grant
1998
- 1998-05-20 US US09/081,782 patent/US6057318A/en not_active Expired - Fee Related
- 1998-05-20 US US09/081,669 patent/US5891893A/en not_active Expired - Fee Related
- 1998-05-20 US US09/081,783 patent/US5891894A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
FR2656610B1 (fr)	1992-05-07
LV5803A4 (lv)	1997-02-20
FR2656610A1 (fr)	1991-07-05
IL96811A0 (en)	1991-09-16
TW215921B (de)	1993-11-11
WO1991009857A1 (fr)	1991-07-11
HUT61761A (en)	1993-03-01
DE69017443D1 (de)	1995-04-06
NZ236678A (en)	1992-06-25
HK1000011A1 (en)	1997-10-03
UA35546C2 (uk)	2001-04-16
RU2049784C1 (ru)	1995-12-10
CZ627790A3 (en)	1996-01-17
SK278810B6 (sk)	1998-03-04
ES2069276T3 (es)	1995-05-01
FI95380C (fi)	1996-01-25
NO179975B (no)	1996-10-14
EP0462264B1 (de)	1995-03-01
PT96368A (pt)	1991-09-30
SK627790A3 (en)	1998-03-04
NO913378L (no)	1991-10-28
EP0462264A1 (de)	1991-12-27
HU912819D0 (en)	1992-02-28
DE69017443T2 (de)	1995-10-12
CA2046883A1 (en)	1991-06-30
DK0462264T3 (da)	1995-05-22
KR920701202A (ko)	1992-08-11
CN1053064A (zh)	1991-07-17
US5470855A (en)	1995-11-28
ZA9010447B (en)	1992-08-26
CZ280803B6 (cs)	1996-04-17
IE67322B1 (en)	1996-03-20
FI914058A0 (fi)	1991-08-28
US5780468A (en)	1998-07-14
NO913378D0 (no)	1991-08-28
CA2046883C (en)	2000-08-15
US6057318A (en)	2000-05-02
US5891894A (en)	1999-04-06
PL167101B1 (pl)	1995-07-31
MX9203019A (es)	1992-08-01
IE904721A1 (en)	1991-07-17
KR0159517B1 (ko)	1998-12-01
AU7055591A (en)	1991-07-24
AU627103B2 (en)	1992-08-13
ATE119160T1 (de)	1995-03-15
JP2758077B2 (ja)	1998-05-25
JPH04504863A (ja)	1992-08-27
CN1028757C (zh)	1995-06-07
FI95380B (fi)	1995-10-13
LV5803B4 (lv)	1997-08-20
BR1100202A (pt)	1999-11-09
US5891893A (en)	1999-04-06
NO179975C (no)	1997-01-22
PT96368B (pt)	1998-06-30
HU213230B (en)	1997-03-28

Legal Events

Date	Code	Title
1997-02-18	KB	Patent renewed
2000-07-26	HC	Change of name of proprietor(s)
2001-04-30	KB	Patent renewed
2005-02-20	KB	Patent renewed
2010-04-08	MM9K	Patent not in force due to non-payment of renewal fees

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