SE458277B - 7-karboximetoxi-furo-(3,4-c)-pyridinderivat, saett foer deras framstaellning och teurapeutiska kompositioner innehaallande desamma - Google Patents
7-karboximetoxi-furo-(3,4-c)-pyridinderivat, saett foer deras framstaellning och teurapeutiska kompositioner innehaallande desammaInfo
- Publication number
- SE458277B SE458277B SE8405754A SE8405754A SE458277B SE 458277 B SE458277 B SE 458277B SE 8405754 A SE8405754 A SE 8405754A SE 8405754 A SE8405754 A SE 8405754A SE 458277 B SE458277 B SE 458277B
- Authority
- SE
- Sweden
- Prior art keywords
- groups
- carbon atoms
- group
- furo
- dihydro
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 4
- 239000000203 mixture Substances 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 22
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- IHWMIFMVQLOHLG-UHFFFAOYSA-N 6-methyl-1,3-dihydrofuro[3,4-c]pyridine Chemical class C1=NC(C)=CC2=C1COC2 IHWMIFMVQLOHLG-UHFFFAOYSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 3
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 21
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000003884 phenylalkyl group Chemical group 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 125000004984 dialkylaminoalkoxy group Chemical group 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 1
- 238000002844 melting Methods 0.000 description 33
- 230000008018 melting Effects 0.000 description 33
- 239000000047 product Substances 0.000 description 18
- 238000000921 elemental analysis Methods 0.000 description 15
- BFJMHTOBRRZELQ-UHFFFAOYSA-N 3-iodo-2h-pyrazolo[3,4-c]pyridine Chemical compound N1=CC=C2C(I)=NNC2=C1 BFJMHTOBRRZELQ-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000700159 Rattus Species 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- COXVTLYNGOIATD-HVMBLDELSA-N CC1=C(C=CC(=C1)C1=CC(C)=C(C=C1)\N=N\C1=C(O)C2=C(N)C(=CC(=C2C=C1)S(O)(=O)=O)S(O)(=O)=O)\N=N\C1=CC=C2C(=CC(=C(N)C2=C1O)S(O)(=O)=O)S(O)(=O)=O Chemical compound CC1=C(C=CC(=C1)C1=CC(C)=C(C=C1)\N=N\C1=C(O)C2=C(N)C(=CC(=C2C=C1)S(O)(=O)=O)S(O)(=O)=O)\N=N\C1=CC=C2C(=CC(=C(N)C2=C1O)S(O)(=O)=O)S(O)(=O)=O COXVTLYNGOIATD-HVMBLDELSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 239000000739 antihistaminic agent Substances 0.000 description 3
- 229960003699 evans blue Drugs 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- -1 1,3-Dihydro-3-octenyl-6-methyl-7-carboxymethoxy-furo- (3,4-c) -pyridine Chemical compound 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- PWWVAXIEGOYWEE-UHFFFAOYSA-N Isophenergan Chemical compound C1=CC=C2N(CC(C)N(C)C)C3=CC=CC=C3SC2=C1 PWWVAXIEGOYWEE-UHFFFAOYSA-N 0.000 description 2
- 108010058846 Ovalbumin Proteins 0.000 description 2
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 description 2
- 230000001387 anti-histamine Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000028709 inflammatory response Effects 0.000 description 2
- 229940092253 ovalbumin Drugs 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- 229960000278 theophylline Drugs 0.000 description 2
- JJKQRSNEGCOSOC-VOTSOKGWSA-N 1-[(e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]-2,3-dihydropyridin-6-one Chemical compound COC1=C(O)C(OC)=CC(\C=C\C(=O)N2C(C=CCC2)=O)=C1 JJKQRSNEGCOSOC-VOTSOKGWSA-N 0.000 description 1
- GHTWTWDSJLSJPA-UHFFFAOYSA-N 2-[(3,6-dimethyl-3-pentyl-1h-furo[3,4-c]pyridin-7-yl)oxy]acetic acid Chemical compound C1=NC(C)=C(OCC(O)=O)C2=C1C(CCCCC)(C)OC2 GHTWTWDSJLSJPA-UHFFFAOYSA-N 0.000 description 1
- BSCJLMOJVKMPLM-UHFFFAOYSA-N 2-[(4-chloro-3,3,6-trimethyl-1h-furo[3,4-c]pyridin-7-yl)oxy]acetic acid Chemical compound CC1=NC(Cl)=C2C(C)(C)OCC2=C1OCC(O)=O BSCJLMOJVKMPLM-UHFFFAOYSA-N 0.000 description 1
- HTVZABPSDHVMDS-UHFFFAOYSA-N 2-[(4-chloro-3,6-dimethyl-3-phenyl-1h-furo[3,4-c]pyridin-7-yl)oxy]acetic acid Chemical compound OC(=O)COC=1C(C)=NC(Cl)=C2C=1COC2(C)C1=CC=CC=C1 HTVZABPSDHVMDS-UHFFFAOYSA-N 0.000 description 1
- LRDLAQUPXWBSJX-UHFFFAOYSA-N 2-[(6-methyl-3-phenyl-1,3-dihydrofuro[3,4-c]pyridin-7-yl)oxy]acetic acid Chemical compound O1CC2=C(OCC(O)=O)C(C)=NC=C2C1C1=CC=CC=C1 LRDLAQUPXWBSJX-UHFFFAOYSA-N 0.000 description 1
- VRQOOJYZQZWYTG-UHFFFAOYSA-N 2-[4-chloro-1-(4-chlorophenyl)-6-methylfuro[3,4-c]pyridin-7-yl]oxyacetic acid Chemical compound ClC1=CC=C(C=C1)C=1OC=C2C(=NC(=C(C2=1)OCC(=O)O)C)Cl VRQOOJYZQZWYTG-UHFFFAOYSA-N 0.000 description 1
- NROQVFMIKHXZEE-UHFFFAOYSA-N 2-[[3-(3-chlorophenyl)-3,6-dimethyl-1H-furo[3,4-c]pyridin-7-yl]oxy]acetic acid Chemical compound ClC=1C=C(C=CC1)C1(OCC2=C1C=NC(=C2OCC(=O)O)C)C NROQVFMIKHXZEE-UHFFFAOYSA-N 0.000 description 1
- SFALQWYGIWKMFS-UHFFFAOYSA-N 2-[[3-(4-chlorophenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-yl]oxy]acetic acid Chemical compound O1CC2=C(OCC(O)=O)C(C)=NC=C2C1C1=CC=C(Cl)C=C1 SFALQWYGIWKMFS-UHFFFAOYSA-N 0.000 description 1
- RHMKBLSGUNJRJY-UHFFFAOYSA-N 2-[[3-(4-fluorophenyl)-3,6-dimethyl-1h-furo[3,4-c]pyridin-7-yl]oxy]acetic acid Chemical compound OC(=O)COC=1C(C)=NC=C2C=1COC2(C)C1=CC=C(F)C=C1 RHMKBLSGUNJRJY-UHFFFAOYSA-N 0.000 description 1
- CLQNYNHDJQJWNT-UHFFFAOYSA-N 2-[[3-(4-fluorophenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-yl]oxy]acetic acid Chemical compound O1CC2=C(OCC(O)=O)C(C)=NC=C2C1C1=CC=C(F)C=C1 CLQNYNHDJQJWNT-UHFFFAOYSA-N 0.000 description 1
- STSQAMJMGVYCOA-UHFFFAOYSA-N 2-[[4-bromo-3-(4-chlorophenyl)-3-ethyl-6-methyl-1h-furo[3,4-c]pyridin-7-yl]oxy]acetic acid Chemical compound O1CC(C(=C(C)N=C2Br)OCC(O)=O)=C2C1(CC)C1=CC=C(Cl)C=C1 STSQAMJMGVYCOA-UHFFFAOYSA-N 0.000 description 1
- SFRMZEBQCDKAKE-UHFFFAOYSA-N 2-[[4-bromo-3-(4-chlorophenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-yl]oxy]acetic acid Chemical compound O1CC2=C(OCC(O)=O)C(C)=NC(Br)=C2C1C1=CC=C(Cl)C=C1 SFRMZEBQCDKAKE-UHFFFAOYSA-N 0.000 description 1
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 1
- KWAHUCNBAOBTNK-UHFFFAOYSA-N 3,6-dimethyl-3-pentyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound C1=NC(C)=C(O)C2=C1C(CCCCC)(C)OC2 KWAHUCNBAOBTNK-UHFFFAOYSA-N 0.000 description 1
- LQEMUWNIWKVWOP-UHFFFAOYSA-N 3-(4-chlorophenyl)-3,6-dimethyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound OC=1C(C)=NC=C2C=1COC2(C)C1=CC=C(Cl)C=C1 LQEMUWNIWKVWOP-UHFFFAOYSA-N 0.000 description 1
- ANEYGXYUZGDDGH-UHFFFAOYSA-N 3-(4-fluorophenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol Chemical compound O1CC2=C(O)C(C)=NC=C2C1C1=CC=C(F)C=C1 ANEYGXYUZGDDGH-UHFFFAOYSA-N 0.000 description 1
- XIUDHWARDNZSSX-UHFFFAOYSA-N 3-butyl-3-ethyl-6-methyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound C1=NC(C)=C(O)C2=C1C(CCCC)(CC)OC2 XIUDHWARDNZSSX-UHFFFAOYSA-N 0.000 description 1
- MEVOEUZLYUNXHS-UHFFFAOYSA-N 3-ethyl-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol Chemical compound C1=NC(C)=C(O)C2=C1C(CC)OC2 MEVOEUZLYUNXHS-UHFFFAOYSA-N 0.000 description 1
- GBXNEXHTLHJCCQ-UHFFFAOYSA-N 4-bromo-3-(4-chlorophenyl)-3,6-dimethyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound OC=1C(C)=NC(Br)=C2C=1COC2(C)C1=CC=C(Cl)C=C1 GBXNEXHTLHJCCQ-UHFFFAOYSA-N 0.000 description 1
- OBNHXVFMYJQKCY-UHFFFAOYSA-N 4-bromo-3-(4-chlorophenyl)-3-ethyl-6-methyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound O1CC(C(=C(C)N=C2Br)O)=C2C1(CC)C1=CC=C(Cl)C=C1 OBNHXVFMYJQKCY-UHFFFAOYSA-N 0.000 description 1
- DBOIDOGSKUFJCP-UHFFFAOYSA-N 4-bromo-3-(4-chlorophenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol Chemical compound O1CC2=C(O)C(C)=NC(Br)=C2C1C1=CC=C(Cl)C=C1 DBOIDOGSKUFJCP-UHFFFAOYSA-N 0.000 description 1
- GFSWLZBRAKTADY-UHFFFAOYSA-N 4-bromo-3-(4-chlorophenyl)-6-methyl-3-propyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound O1CC(C(=C(C)N=C2Br)O)=C2C1(CCC)C1=CC=C(Cl)C=C1 GFSWLZBRAKTADY-UHFFFAOYSA-N 0.000 description 1
- WYAPBLOJYSXOBY-UHFFFAOYSA-N 4-bromo-3-(4-methoxyphenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol Chemical compound C1=CC(OC)=CC=C1C1C(C(Br)=NC(C)=C2O)=C2CO1 WYAPBLOJYSXOBY-UHFFFAOYSA-N 0.000 description 1
- TUQIOGCEVRUMIX-UHFFFAOYSA-N 4-chloro-1-methoxy-3-(4-methoxyphenyl)-6-methyl-1,3-dihydrofuro[3,4-c]pyridine-7-carboxylic acid Chemical compound COC1=CC=C(C=C1)C1OC(C2=C1C(=NC(=C2C(=O)O)C)Cl)OC TUQIOGCEVRUMIX-UHFFFAOYSA-N 0.000 description 1
- JNXCOPPTXGMZCF-UHFFFAOYSA-N 4-chloro-3,3-bis(4-chlorophenyl)-6-methyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound OC=1C(C)=NC(Cl)=C2C=1COC2(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 JNXCOPPTXGMZCF-UHFFFAOYSA-N 0.000 description 1
- MZLLECZYEGRZSK-UHFFFAOYSA-N 4-chloro-3,6-dimethyl-3-phenyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound OC=1C(C)=NC(Cl)=C2C=1COC2(C)C1=CC=CC=C1 MZLLECZYEGRZSK-UHFFFAOYSA-N 0.000 description 1
- WAPRDIBFQJJVIA-UHFFFAOYSA-N 6,7-dimethoxy-3-[3-(trifluoromethyl)anilino]-3h-2-benzofuran-1-one Chemical compound O1C(=O)C2=C(OC)C(OC)=CC=C2C1NC1=CC=CC(C(F)(F)F)=C1 WAPRDIBFQJJVIA-UHFFFAOYSA-N 0.000 description 1
- MIZMBPVMDKMQQN-UHFFFAOYSA-N 6-methyl-3-(4-methylphenyl)-3-phenyl-1h-furo[3,4-c]pyridin-7-ol Chemical compound C1=CC(C)=CC=C1C1(C=2C=CC=CC=2)C(C=NC(C)=C2O)=C2CO1 MIZMBPVMDKMQQN-UHFFFAOYSA-N 0.000 description 1
- AWSNANLRLHTJCZ-UHFFFAOYSA-N 6-methyl-3-phenyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol Chemical compound O1CC2=C(O)C(C)=NC=C2C1C1=CC=CC=C1 AWSNANLRLHTJCZ-UHFFFAOYSA-N 0.000 description 1
- 206010002198 Anaphylactic reaction Diseases 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- HOKDBMAJZXIPGC-UHFFFAOYSA-N Mequitazine Chemical compound C12=CC=CC=C2SC2=CC=CC=C2N1CC1C(CC2)CCN2C1 HOKDBMAJZXIPGC-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 208000004880 Polyuria Diseases 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 206010046996 Varicose vein Diseases 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000036783 anaphylactic response Effects 0.000 description 1
- 208000003455 anaphylaxis Diseases 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000035619 diuresis Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 210000000548 hind-foot Anatomy 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- PPZMYIBUHIPZOS-UHFFFAOYSA-N histamine dihydrochloride Chemical compound Cl.Cl.NCCC1=CN=CN1 PPZMYIBUHIPZOS-UHFFFAOYSA-N 0.000 description 1
- 229960000645 histamine hydrochloride Drugs 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 229960005042 mequitazine Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 210000005164 penile vein Anatomy 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 208000027185 varicose disease Diseases 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D497/04—Ortho-condensed systems
-
- 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
- A61P7/10—Antioedematous agents; Diuretics
-
- 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
- A61P9/12—Antihypertensives
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB838330658A GB8330658D0 (en) | 1983-11-17 | 1983-11-17 | 7-carboxymethoxy-furo-(3,4-c)-pyridine derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8405754D0 SE8405754D0 (sv) | 1984-11-16 |
| SE8405754L SE8405754L (sv) | 1985-05-18 |
| SE458277B true SE458277B (sv) | 1989-03-13 |
Family
ID=10551897
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8405754A SE458277B (sv) | 1983-11-17 | 1984-11-16 | 7-karboximetoxi-furo-(3,4-c)-pyridinderivat, saett foer deras framstaellning och teurapeutiska kompositioner innehaallande desamma |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US4569938A (cs) |
| JP (1) | JPS60116685A (cs) |
| AT (1) | AT391868B (cs) |
| BE (1) | BE900941A (cs) |
| CA (1) | CA1257272A (cs) |
| CH (1) | CH660737A5 (cs) |
| DE (1) | DE3441975A1 (cs) |
| DK (1) | DK157932C (cs) |
| DZ (1) | DZ702A1 (cs) |
| ES (1) | ES8600300A1 (cs) |
| FI (1) | FI80701C (cs) |
| FR (2) | FR2555049B1 (cs) |
| GB (2) | GB8330658D0 (cs) |
| HK (1) | HK77987A (cs) |
| IE (1) | IE58097B1 (cs) |
| IT (1) | IT1177185B (cs) |
| LU (1) | LU85634A1 (cs) |
| MA (1) | MA20263A1 (cs) |
| MY (1) | MY100665A (cs) |
| NL (1) | NL8403318A (cs) |
| OA (1) | OA07865A (cs) |
| SE (1) | SE458277B (cs) |
| SG (1) | SG52687G (cs) |
| ZA (1) | ZA848128B (cs) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8402740D0 (en) * | 1984-02-02 | 1984-03-07 | Scras | Furo-(3 4-c)-pyridine derivatives |
| GB8808001D0 (en) * | 1988-04-06 | 1988-05-05 | Scras | Stereospecific preparative process for furol(3,4-c)pyridine derivatives |
| GB8907480D0 (en) * | 1989-04-03 | 1989-05-17 | Scaras Societe De Conseils De | Separation of insomers of furo(3,4-c)pyridine derivatives |
| US5130252A (en) * | 1990-05-14 | 1992-07-14 | Synthetech, Inc. | Resolution of furopyridine enantiomers and synthetic precursors thereof |
| WO2000053606A1 (en) * | 1999-03-08 | 2000-09-14 | Medicure Inc. | Pyridoxal analogues for vitamin b-6 disorders |
| CA2376029A1 (en) | 1999-07-13 | 2001-01-18 | Medicure Inc. | Use of pyridoxin derivatives for the treatment of diabetes and related complications |
| EP1872797A3 (en) * | 1999-08-24 | 2008-04-02 | Medicure International Inc. | Treatment of cardiovascular and related pathologies |
| CA2401655C (en) | 2000-02-29 | 2010-06-22 | Medicure International Inc. | Cardioprotective phosphonates and malonates |
| US7442689B2 (en) * | 2000-02-29 | 2008-10-28 | Medicure International Inc. | Cardioprotective phosphonates and malonates |
| AU784840B2 (en) | 2000-03-28 | 2006-07-06 | Medicure International Inc. | Treatment of cerebrovascular disease |
| EP1299358B1 (en) | 2000-07-07 | 2007-06-13 | Medicure International Inc. | Pyridoxine and pyridoxal analogues as cardiovascular therapeutics |
| US6897228B2 (en) | 2000-07-07 | 2005-05-24 | Medicure International Inc. | Pyridoxine and pyridoxal analogues: new uses |
| US6548519B1 (en) | 2001-07-06 | 2003-04-15 | Medicure International Inc. | Pyridoxine and pyridoxal analogues: novel uses |
| US20040121988A1 (en) * | 2001-03-28 | 2004-06-24 | Medicure International Inc. | Treatment of cerebrovascular disease |
| US20040186077A1 (en) * | 2003-03-17 | 2004-09-23 | Medicure International Inc. | Novel heteroaryl phosphonates as cardioprotective agents |
| JP2008505126A (ja) * | 2004-07-07 | 2008-02-21 | メディキュア インターナショナル インコーポレイテッド | 血小板凝集薬を用いる併用療法 |
| US20070060549A1 (en) * | 2004-08-10 | 2007-03-15 | Friesen Albert D | Combination therapies employing ace inhibitors and uses thereof for the treatment of diabetic disorders |
| WO2006050598A1 (en) * | 2004-10-28 | 2006-05-18 | Medicure International Inc. | Dual antiplatelet/anticoagulant pyridoxine analogs |
| US7459468B2 (en) * | 2004-10-28 | 2008-12-02 | Medicure International, Inc. | Aryl sulfonic pyridoxines as antiplatelet agents |
| US20060094749A1 (en) * | 2004-10-28 | 2006-05-04 | Medicure International Inc. | Substituted pyridoxines as anti-platelet agents |
| US20070105817A1 (en) * | 2005-11-09 | 2007-05-10 | Jim Page | Use of cicletanine and other furopyridines for treatment of systolic-predominant hypertension, isolated systolic hypertension, elevated pulse pressure, and general hypertension |
| AU2006317440A1 (en) * | 2005-11-28 | 2007-05-31 | Medicure International Inc. | Selected dosage for the treatment of cardiovascular and related pathologies |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT297442B (de) * | 1970-04-01 | 1972-03-27 | Unilever Nv | Verfahren zum Reinigen, Entfetten, Entzundern und Beizen von Metallen |
| GB2008582B (en) * | 1977-11-25 | 1982-04-28 | Scras | Pyridine derivative |
| ZA786269B (en) * | 1977-11-25 | 1979-10-31 | Scras | New pyridine derivative,its preparation and use |
| IN156817B (cs) * | 1981-02-10 | 1985-11-09 | Scras |
-
1983
- 1983-11-17 GB GB838330658A patent/GB8330658D0/en active Pending
-
1984
- 1984-10-17 ZA ZA848128A patent/ZA848128B/xx unknown
- 1984-10-19 GB GB08426489A patent/GB2149781B/en not_active Expired
- 1984-10-26 CH CH5127/84A patent/CH660737A5/fr not_active IP Right Cessation
- 1984-10-30 BE BE0/213925A patent/BE900941A/fr not_active IP Right Cessation
- 1984-11-01 NL NL8403318A patent/NL8403318A/nl not_active Application Discontinuation
- 1984-11-05 US US06/668,394 patent/US4569938A/en not_active Expired - Lifetime
- 1984-11-07 LU LU85634A patent/LU85634A1/fr unknown
- 1984-11-08 FI FI844383A patent/FI80701C/fi not_active IP Right Cessation
- 1984-11-08 MA MA20487A patent/MA20263A1/fr unknown
- 1984-11-14 CA CA000467829A patent/CA1257272A/en not_active Expired
- 1984-11-14 DZ DZ847329A patent/DZ702A1/fr active
- 1984-11-14 IT IT23564/84A patent/IT1177185B/it active
- 1984-11-15 ES ES537666A patent/ES8600300A1/es not_active Expired
- 1984-11-16 JP JP59240900A patent/JPS60116685A/ja active Granted
- 1984-11-16 DK DK545684A patent/DK157932C/da not_active IP Right Cessation
- 1984-11-16 SE SE8405754A patent/SE458277B/sv not_active IP Right Cessation
- 1984-11-16 IE IE294784A patent/IE58097B1/en not_active IP Right Cessation
- 1984-11-16 OA OA58442A patent/OA07865A/xx unknown
- 1984-11-16 DE DE19843441975 patent/DE3441975A1/de active Granted
- 1984-11-16 FR FR8417479A patent/FR2555049B1/fr not_active Expired
- 1984-11-16 FR FR8417478A patent/FR2555181B1/fr not_active Expired
- 1984-11-19 AT AT0365584A patent/AT391868B/de not_active IP Right Cessation
-
1987
- 1987-06-17 SG SG52687A patent/SG52687G/en unknown
- 1987-07-01 MY MYPI87000926A patent/MY100665A/en unknown
- 1987-10-22 HK HK779/87A patent/HK77987A/xx not_active IP Right Cessation
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