SE448234B - Derivat av 1,2,4-oxadiazin, sett for deras framstellning och farmaceutiska beredningar innehallande dem - Google Patents
Derivat av 1,2,4-oxadiazin, sett for deras framstellning och farmaceutiska beredningar innehallande demInfo
- Publication number
- SE448234B SE448234B SE8007026A SE8007026A SE448234B SE 448234 B SE448234 B SE 448234B SE 8007026 A SE8007026 A SE 8007026A SE 8007026 A SE8007026 A SE 8007026A SE 448234 B SE448234 B SE 448234B
- Authority
- SE
- Sweden
- Prior art keywords
- general formula
- alkyl
- oxadiazine
- compound
- dihydro
- Prior art date
Links
- 239000000825 pharmaceutical preparation Substances 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title claims description 4
- 150000005065 1,2,4-oxadiazines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 42
- 229910052739 hydrogen Chemical group 0.000 claims description 37
- -1 sulfonyloxy Chemical group 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 239000001257 hydrogen Chemical group 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000002367 halogens Chemical class 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- AMYBENVFIQCYHW-UHFFFAOYSA-N 6-(3,4-dihydro-1h-isoquinolin-2-yl)-4-methyl-3-phenyl-5,6-dihydro-1,2,4-oxadiazine Chemical compound CN1CC(N2CC3=CC=CC=C3CC2)ON=C1C1=CC=CC=C1 AMYBENVFIQCYHW-UHFFFAOYSA-N 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- MEOYAFZJCQHMDA-UHFFFAOYSA-N 6-(3,4-dihydro-1h-isoquinolin-2-yl)-3-(2,2-diphenylethyl)-4-methyl-5,6-dihydro-1,2,4-oxadiazine Chemical compound CN1CC(N2CC3=CC=CC=C3CC2)ON=C1CC(C=1C=CC=CC=1)C1=CC=CC=C1 MEOYAFZJCQHMDA-UHFFFAOYSA-N 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 230000003288 anthiarrhythmic effect Effects 0.000 claims description 2
- 239000002585 base Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- AYBGUJTXFNOCHC-UHFFFAOYSA-N n-[[3-(2,2-diphenylethyl)-5,6-dihydro-2h-1,2,4-oxadiazin-6-yl]methyl]cyclohexanamine Chemical compound C1N=C(CC(C=2C=CC=CC=2)C=2C=CC=CC=2)NOC1CNC1CCCCC1 AYBGUJTXFNOCHC-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- RXCMFQDTWCCLBL-UHFFFAOYSA-N 4-amino-3-hydroxynaphthalene-1-sulfonic acid Chemical class C1=CC=C2C(N)=C(O)C=C(S(O)(=O)=O)C2=C1 RXCMFQDTWCCLBL-UHFFFAOYSA-N 0.000 claims 1
- CVHVYMQHSMXBMH-UHFFFAOYSA-N 6-(3,4-dihydro-1h-isoquinolin-2-yl)-4-methyl-3-(4-methylphenyl)-5,6-dihydro-1,2,4-oxadiazine Chemical compound CN1CC(N2CC3=CC=CC=C3CC2)ON=C1C1=CC=C(C)C=C1 CVHVYMQHSMXBMH-UHFFFAOYSA-N 0.000 claims 1
- 101100298295 Drosophila melanogaster flfl gene Proteins 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 239000012050 conventional carrier Substances 0.000 claims 1
- 239000002934 diuretic Substances 0.000 claims 1
- 230000001882 diuretic effect Effects 0.000 claims 1
- DJLVSILRWJFIPB-UHFFFAOYSA-N n-[(3-phenyl-5,6-dihydro-2h-1,2,4-oxadiazin-6-yl)methyl]cyclohexanamine Chemical compound C1NC(C=2C=CC=CC=2)=NOC1CNC1CCCCC1 DJLVSILRWJFIPB-UHFFFAOYSA-N 0.000 claims 1
- NAXHSOYAROJFOD-UHFFFAOYSA-N n-cyclohexyl-3-(2,2-diphenylethyl)-n,4-dimethyl-5,6-dihydro-1,2,4-oxadiazin-6-amine Chemical compound C1N(C)C(CC(C=2C=CC=CC=2)C=2C=CC=CC=2)=NOC1N(C)C1CCCCC1 NAXHSOYAROJFOD-UHFFFAOYSA-N 0.000 claims 1
- 230000000304 vasodilatating effect Effects 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 42
- 238000002844 melting Methods 0.000 description 30
- 230000008018 melting Effects 0.000 description 30
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 24
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 21
- 229910052757 nitrogen Inorganic materials 0.000 description 21
- 229910052799 carbon Inorganic materials 0.000 description 19
- 239000000243 solution Substances 0.000 description 18
- UWYZHKAOTLEWKK-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2CNCCC2=C1 UWYZHKAOTLEWKK-UHFFFAOYSA-N 0.000 description 17
- 239000011541 reaction mixture Substances 0.000 description 17
- 239000000047 product Substances 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
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- 238000012986 modification Methods 0.000 description 12
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- 241000699670 Mus sp. Species 0.000 description 8
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- 230000037396 body weight Effects 0.000 description 6
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- 230000017531 blood circulation Effects 0.000 description 5
- 230000036772 blood pressure Effects 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 125000000579 2,2-diphenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])* 0.000 description 4
- WZJCDAHJVIMHRG-UHFFFAOYSA-N 6-(chloromethyl)-3-phenyl-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound N1OC(CCl)CN=C1C1=CC=CC=C1 WZJCDAHJVIMHRG-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 241000282326 Felis catus Species 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000282472 Canis lupus familiaris Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 206010030113 Oedema Diseases 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- UWOIYSYQXABWQU-UHFFFAOYSA-N 3-(4-chlorophenyl)-6-(3,4-dihydro-1h-isoquinolin-2-yl)-4-methyl-5,6-dihydro-1,2,4-oxadiazine Chemical compound CN1CC(N2CC3=CC=CC=C3CC2)ON=C1C1=CC=C(Cl)C=C1 UWOIYSYQXABWQU-UHFFFAOYSA-N 0.000 description 2
- 229920002307 Dextran Polymers 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Chemical compound 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
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
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- 238000000605 extraction Methods 0.000 description 2
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- 230000000977 initiatory effect Effects 0.000 description 2
- 238000007912 intraperitoneal administration Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- PRXWSCNYUBDAJJ-UHFFFAOYSA-N n-cyclohexyl-n,4-dimethyl-3-phenyl-5,6-dihydro-1,2,4-oxadiazin-6-amine;dihydrochloride Chemical compound Cl.Cl.C1N(C)C(C=2C=CC=CC=2)=NOC1N(C)C1CCCCC1 PRXWSCNYUBDAJJ-UHFFFAOYSA-N 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 210000002700 urine Anatomy 0.000 description 2
- VAZSYRRTLMMEQO-UHFFFAOYSA-N (3-phenyl-5,6-dihydro-2h-1,2,4-oxadiazin-6-yl)methyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCC1ON=C(C=2C=CC=CC=2)NC1 VAZSYRRTLMMEQO-UHFFFAOYSA-N 0.000 description 1
- BZHOKQANGBITDK-UHFFFAOYSA-N (3-phenyl-5,6-dihydro-2h-1,2,4-oxadiazin-6-yl)methyl methanesulfonate Chemical compound O1C(COS(=O)(=O)C)CNC(C=2C=CC=CC=2)=N1 BZHOKQANGBITDK-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- QXXDFOOHJPTYJD-UHFFFAOYSA-N 1-methoxy-1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2C(OC)NCCC2=C1 QXXDFOOHJPTYJD-UHFFFAOYSA-N 0.000 description 1
- WWHPCFPYBGJSGW-UHFFFAOYSA-N 2h-1,2,4-oxadiazin-6-ylmethanol Chemical class OCC1=CN=CNO1 WWHPCFPYBGJSGW-UHFFFAOYSA-N 0.000 description 1
- QMEQBOSUJUOXMX-UHFFFAOYSA-N 2h-oxadiazine Chemical compound N1OC=CC=N1 QMEQBOSUJUOXMX-UHFFFAOYSA-N 0.000 description 1
- KVMQLWOQLDVSOB-UHFFFAOYSA-N 6-(3,4-dihydro-1h-isoquinolin-2-yl)-4-methyl-3-(4-methylphenyl)-5,6-dihydro-1,2,4-oxadiazine;dihydrochloride Chemical compound Cl.Cl.CN1CC(N2CC3=CC=CC=C3CC2)ON=C1C1=CC=C(C)C=C1 KVMQLWOQLDVSOB-UHFFFAOYSA-N 0.000 description 1
- GWAKPCRBHTWEKQ-UHFFFAOYSA-N 6-(3,4-dihydro-1h-isoquinolin-2-ylmethyl)-3-phenyl-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound C1CC2=CC=CC=C2CN1CC(ON1)CN=C1C1=CC=CC=C1 GWAKPCRBHTWEKQ-UHFFFAOYSA-N 0.000 description 1
- YLAZUWQGSLGBFA-UHFFFAOYSA-N 6-(6,7-dimethoxy-3,4-dihydro-1h-isoquinolin-2-yl)-4-methyl-3-phenyl-5,6-dihydro-1,2,4-oxadiazine Chemical compound C1C=2C=C(OC)C(OC)=CC=2CCN1C(ON=1)CN(C)C=1C1=CC=CC=C1 YLAZUWQGSLGBFA-UHFFFAOYSA-N 0.000 description 1
- OESDPEGYHLAMKJ-UHFFFAOYSA-N 6-(chloromethyl)-3-(2,2-diphenylethyl)-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound O1C(CCl)CNC(CC(C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 OESDPEGYHLAMKJ-UHFFFAOYSA-N 0.000 description 1
- YDAYWCCXGRSSAF-UHFFFAOYSA-N 6-(chloromethyl)-3-(2-chlorophenyl)-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound O1C(CCl)CNC(C=2C(=CC=CC=2)Cl)=N1 YDAYWCCXGRSSAF-UHFFFAOYSA-N 0.000 description 1
- CGTKHFWNDRXXRB-UHFFFAOYSA-N 6-(chloromethyl)-3-(2-methylpropyl)-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound CC(C)CC1=NOC(CCl)CN1 CGTKHFWNDRXXRB-UHFFFAOYSA-N 0.000 description 1
- MBQFYXOFZRKUAZ-UHFFFAOYSA-N 6-(chloromethyl)-3-(4-chlorophenyl)-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound O1C(CCl)CNC(C=2C=CC(Cl)=CC=2)=N1 MBQFYXOFZRKUAZ-UHFFFAOYSA-N 0.000 description 1
- YDQCVAWETLXNQE-UHFFFAOYSA-N 6-(chloromethyl)-3-(4-methylphenyl)-5,6-dihydro-2h-1,2,4-oxadiazine Chemical compound C1=CC(C)=CC=C1C1=NOC(CCl)CN1 YDQCVAWETLXNQE-UHFFFAOYSA-N 0.000 description 1
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- XSFSCSFTIPFCSG-UHFFFAOYSA-N [3-(2,2-diphenylethyl)-5,6-dihydro-2h-1,2,4-oxadiazin-6-yl]methyl methanesulfonate Chemical compound O1C(COS(=O)(=O)C)CNC(CC(C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 XSFSCSFTIPFCSG-UHFFFAOYSA-N 0.000 description 1
- UNQBYEXQULCBAN-UHFFFAOYSA-N [6-(3,4-dihydro-1h-isoquinolin-2-yl)-5-methyl-3-phenyl-5,6-dihydro-1,2,4-oxadiazin-4-yl]-phenylmethanone Chemical compound CC1C(N2CC3=CC=CC=C3CC2)ON=C(C=2C=CC=CC=2)N1C(=O)C1=CC=CC=C1 UNQBYEXQULCBAN-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
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- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
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- MVPPADPHJFYWMZ-IDEBNGHGSA-N chlorobenzene Chemical group Cl[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 MVPPADPHJFYWMZ-IDEBNGHGSA-N 0.000 description 1
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- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
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- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- STQHSZJHWVTWSC-UHFFFAOYSA-N n-[(3-phenyl-5,6-dihydro-2h-1,2,4-oxadiazin-6-yl)methyl]cyclohexanamine;dihydrochloride Chemical compound Cl.Cl.C1NC(C=2C=CC=CC=2)=NOC1CNC1CCCCC1 STQHSZJHWVTWSC-UHFFFAOYSA-N 0.000 description 1
- YRKKMZNNTCJWQM-UHFFFAOYSA-N n-cyclohexyl-3-(2,2-diphenylethyl)-n,4-dimethyl-5,6-dihydro-1,2,4-oxadiazin-6-amine;dihydrochloride Chemical compound Cl.Cl.C1N(C)C(CC(C=2C=CC=CC=2)C=2C=CC=CC=2)=NOC1N(C)C1CCCCC1 YRKKMZNNTCJWQM-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
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- 150000005063 oxadiazines Chemical class 0.000 description 1
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- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/04—Six-membered rings
-
- 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
- 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
-
- 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
-
- 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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU79CI1914A HU180708B (en) | 1979-10-11 | 1979-10-11 | Process for preparing new 1,2,4-oxadiazine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8007026L SE8007026L (sv) | 1981-04-12 |
| SE448234B true SE448234B (sv) | 1987-02-02 |
Family
ID=10994765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8007026A SE448234B (sv) | 1979-10-11 | 1980-10-07 | Derivat av 1,2,4-oxadiazin, sett for deras framstellning och farmaceutiska beredningar innehallande dem |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4308270A (en, 2012) |
| JP (1) | JPS5663970A (en, 2012) |
| AT (1) | AT373247B (en, 2012) |
| BE (1) | BE885634A (en, 2012) |
| CA (1) | CA1159828A (en, 2012) |
| CH (1) | CH649540A5 (en, 2012) |
| CS (1) | CS249111B2 (en, 2012) |
| DD (1) | DD153551A5 (en, 2012) |
| DE (1) | DE3037747A1 (en, 2012) |
| DK (1) | DK149106C (en, 2012) |
| ES (1) | ES495820A0 (en, 2012) |
| FR (1) | FR2467204B1 (en, 2012) |
| GB (1) | GB2062628B (en, 2012) |
| GR (1) | GR71205B (en, 2012) |
| HU (1) | HU180708B (en, 2012) |
| IL (1) | IL61176A (en, 2012) |
| IT (1) | IT1129306B (en, 2012) |
| LU (1) | LU82823A1 (en, 2012) |
| NL (1) | NL8005587A (en, 2012) |
| NO (1) | NO153652C (en, 2012) |
| PL (2) | PL129378B1 (en, 2012) |
| RO (3) | RO85268B (en, 2012) |
| SE (1) | SE448234B (en, 2012) |
| SU (1) | SU1087520A1 (en, 2012) |
| YU (2) | YU41739B (en, 2012) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU179951B (en) * | 1979-10-11 | 1983-01-28 | Chinoin Gyogyszer Es Vegyeszet | Process for preparing 1,2,4-oxadiazolin-5-one derivatives and pharmaceutical compositions containing thereof |
| WO2004091547A2 (en) * | 2003-04-10 | 2004-10-28 | Cytokinetics, Inc | Compounds, compositions, and methods |
| WO2017031325A1 (en) * | 2015-08-18 | 2017-02-23 | Forum Pharmaceuticals Inc. | Oxadiazine compounds and methods of use thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL132134C (en, 2012) * | 1963-03-22 | |||
| DE1545658C3 (de) * | 1964-03-02 | 1981-04-23 | Chinoin Gyógyszer és Vegyészeti Termékek Gyára RT, 1045 Budapest | Verfahren zur Herstellung von 3,5-disubstituierten 1,2,4-Oxadiazolderivaten |
| DE1795839C3 (de) * | 1964-03-02 | 1981-09-03 | Chinoin Gyógyszer és Vegyészeti Termékek Gyára RT, 1045 Budapest | Verfahren zur Herstellung von 3,5-disubstituierten 1,2,4-Oxadiazolderivaten |
| IT1043838B (it) * | 1971-04-22 | 1980-02-29 | Poli Ind Chimica Spa | 1 2 3 4 tetraidroisochinoline e processo per la loro preparazione |
| US4154598A (en) * | 1975-09-11 | 1979-05-15 | Philagro | Herbicidal 1,2,4-oxadiazin-5-one compositions |
| US4026894A (en) * | 1975-10-14 | 1977-05-31 | Abbott Laboratories | Antihypertensive agents |
| HU179951B (en) * | 1979-10-11 | 1983-01-28 | Chinoin Gyogyszer Es Vegyeszet | Process for preparing 1,2,4-oxadiazolin-5-one derivatives and pharmaceutical compositions containing thereof |
-
1979
- 1979-10-11 HU HU79CI1914A patent/HU180708B/hu not_active IP Right Cessation
-
1980
- 1980-09-30 IL IL61176A patent/IL61176A/xx unknown
- 1980-10-03 LU LU82823A patent/LU82823A1/de unknown
- 1980-10-06 CS CS806736A patent/CS249111B2/cs unknown
- 1980-10-06 DE DE19803037747 patent/DE3037747A1/de not_active Withdrawn
- 1980-10-06 GR GR63060A patent/GR71205B/el unknown
- 1980-10-07 SE SE8007026A patent/SE448234B/sv not_active IP Right Cessation
- 1980-10-09 AT AT0501280A patent/AT373247B/de not_active IP Right Cessation
- 1980-10-09 NL NL8005587A patent/NL8005587A/nl not_active Application Discontinuation
- 1980-10-09 RO RO108149A patent/RO85268B/ro unknown
- 1980-10-09 IT IT68556/80A patent/IT1129306B/it active
- 1980-10-09 RO RO80102322A patent/RO81210A/ro unknown
- 1980-10-09 FR FR8021625A patent/FR2467204B1/fr not_active Expired
- 1980-10-09 JP JP14066980A patent/JPS5663970A/ja active Granted
- 1980-10-09 RO RO108150A patent/RO85269B/ro unknown
- 1980-10-10 SU SU802993202A patent/SU1087520A1/ru active
- 1980-10-10 US US06/196,034 patent/US4308270A/en not_active Expired - Lifetime
- 1980-10-10 BE BE0/202407A patent/BE885634A/fr not_active IP Right Cessation
- 1980-10-10 CH CH7600/80A patent/CH649540A5/de not_active IP Right Cessation
- 1980-10-10 ES ES495820A patent/ES495820A0/es active Granted
- 1980-10-10 NO NO803045A patent/NO153652C/no unknown
- 1980-10-10 YU YU2595/80A patent/YU41739B/xx unknown
- 1980-10-10 DD DD80224477A patent/DD153551A5/de not_active IP Right Cessation
- 1980-10-10 DK DK429680A patent/DK149106C/da not_active IP Right Cessation
- 1980-10-10 GB GB8032827A patent/GB2062628B/en not_active Expired
- 1980-10-10 PL PL1980232264A patent/PL129378B1/pl unknown
- 1980-10-10 PL PL1980227211A patent/PL129081B1/pl unknown
- 1980-10-10 CA CA000362230A patent/CA1159828A/en not_active Expired
-
1982
- 1982-12-29 YU YU2911/82A patent/YU42063B/xx unknown
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| NUG | Patent has lapsed |
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