CA1051924A - Composes arylsulfonylcarbamoyl dicarbonyl-1,3 alicycliques et arylsulfonylcarbamoyl dicarbonyl-1,3 acycliques - Google Patents
Composes arylsulfonylcarbamoyl dicarbonyl-1,3 alicycliques et arylsulfonylcarbamoyl dicarbonyl-1,3 acycliquesInfo
- Publication number
- CA1051924A CA1051924A CA227,783A CA227783A CA1051924A CA 1051924 A CA1051924 A CA 1051924A CA 227783 A CA227783 A CA 227783A CA 1051924 A CA1051924 A CA 1051924A
- Authority
- CA
- Canada
- Prior art keywords
- cyclohexanedione
- pharmaceutically acceptable
- basic salt
- acceptable basic
- compound
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 45
- 239000000126 substance Substances 0.000 claims abstract description 23
- XAPKRXDEHGLXGL-UHFFFAOYSA-N n-(4-chlorophenyl)sulfonyl-4,4-dimethyl-2,6-dioxocyclohexane-1-carboxamide Chemical compound O=C1CC(C)(C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 XAPKRXDEHGLXGL-UHFFFAOYSA-N 0.000 claims abstract description 4
- QLXKYKBCVAABLB-UHFFFAOYSA-N n-(4-chlorophenyl)sulfonyl-2,6-dioxo-4-pentan-3-ylcyclohexane-1-carboxamide Chemical compound O=C1CC(C(CC)CC)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 QLXKYKBCVAABLB-UHFFFAOYSA-N 0.000 claims abstract 3
- 238000000034 method Methods 0.000 claims description 66
- 150000001447 alkali salts Chemical class 0.000 claims description 44
- VLJQDHDVZJXNQL-UHFFFAOYSA-N 4-methyl-n-(oxomethylidene)benzenesulfonamide Chemical compound CC1=CC=C(S(=O)(=O)N=C=O)C=C1 VLJQDHDVZJXNQL-UHFFFAOYSA-N 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- JGHDVROWMPBQSR-UHFFFAOYSA-N 4-chloro-n-(oxomethylidene)benzenesulfonamide Chemical compound ClC1=CC=C(S(=O)(=O)N=C=O)C=C1 JGHDVROWMPBQSR-UHFFFAOYSA-N 0.000 claims description 5
- DUKZQEYDAFUJMK-UHFFFAOYSA-N 5-propan-2-ylcyclohexane-1,3-dione Chemical compound CC(C)C1CC(=O)CC(=O)C1 DUKZQEYDAFUJMK-UHFFFAOYSA-N 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- LHODCNACHFRUQN-UHFFFAOYSA-N 4-ethyl-n-(4-methylphenyl)sulfonyl-2,6-dioxocyclohexane-1-carboxamide Chemical compound O=C1CC(CC)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 LHODCNACHFRUQN-UHFFFAOYSA-N 0.000 claims description 4
- BADXJIPKFRBFOT-UHFFFAOYSA-N dimedone Chemical compound CC1(C)CC(=O)CC(=O)C1 BADXJIPKFRBFOT-UHFFFAOYSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- UJYAZVSPFMJCLW-UHFFFAOYSA-N n-(oxomethylidene)benzenesulfonamide Chemical compound O=C=NS(=O)(=O)C1=CC=CC=C1 UJYAZVSPFMJCLW-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- JGFWOERKVHJLHQ-UHFFFAOYSA-N n-(4-methylphenyl)sulfonyl-2,6-dioxo-4-phenylcyclohexane-1-carboxamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)C1C(=O)CC(C=2C=CC=CC=2)CC1=O JGFWOERKVHJLHQ-UHFFFAOYSA-N 0.000 claims description 3
- JFPGNCHSCYHDCC-UHFFFAOYSA-N n-(4-methylphenyl)sulfonyl-2,6-dioxo-4-propan-2-ylcyclohexane-1-carboxamide Chemical compound O=C1CC(C(C)C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 JFPGNCHSCYHDCC-UHFFFAOYSA-N 0.000 claims description 3
- KZEOINSFZQMGOV-UHFFFAOYSA-N n-(4-methylphenyl)sulfonyl-2,6-dioxo-4-propylcyclohexane-1-carboxamide Chemical compound O=C1CC(CCC)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 KZEOINSFZQMGOV-UHFFFAOYSA-N 0.000 claims description 3
- QHMPQSYRALVILC-UHFFFAOYSA-N n-(4-methylphenyl)sulfonyl-4-(2-methylpropyl)-2,6-dioxocyclohexane-1-carboxamide Chemical compound O=C1CC(CC(C)C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 QHMPQSYRALVILC-UHFFFAOYSA-N 0.000 claims description 3
- UQNDMNHJULEGKX-UHFFFAOYSA-N n-(benzenesulfonyl)-2,6-dioxo-4-propan-2-ylcyclohexane-1-carboxamide Chemical compound O=C1CC(C(C)C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=CC=C1 UQNDMNHJULEGKX-UHFFFAOYSA-N 0.000 claims description 3
- BUXTXUBQAKIQKS-UHFFFAOYSA-N sulfuryl diisocyanate Chemical compound O=C=NS(=O)(=O)N=C=O BUXTXUBQAKIQKS-UHFFFAOYSA-N 0.000 claims description 3
- LQNQODXUTPLCGH-UHFFFAOYSA-N 5-(2-methylpropyl)cyclohexane-1,3-dione Chemical compound CC(C)CC1CC(=O)CC(=O)C1 LQNQODXUTPLCGH-UHFFFAOYSA-N 0.000 claims description 2
- VPRYSOJVBSTQKE-UHFFFAOYSA-N 5-ethylcyclohexane-1,3-dione Chemical compound CCC1CC(=O)CC(=O)C1 VPRYSOJVBSTQKE-UHFFFAOYSA-N 0.000 claims description 2
- ARHIIRZQTUSYIX-UHFFFAOYSA-N 5-pentan-3-ylcyclohexane-1,3-dione Chemical compound CCC(CC)C1CC(=O)CC(=O)C1 ARHIIRZQTUSYIX-UHFFFAOYSA-N 0.000 claims description 2
- UPPYKNLSSLIIAZ-UHFFFAOYSA-N 5-phenylcyclohexane-1,3-dione Chemical compound C1C(=O)CC(=O)CC1C1=CC=CC=C1 UPPYKNLSSLIIAZ-UHFFFAOYSA-N 0.000 claims description 2
- UODQIYOHASHZDQ-UHFFFAOYSA-N 5-tert-butylcyclohexane-1,3-dione Chemical compound CC(C)(C)C1CC(=O)CC(=O)C1 UODQIYOHASHZDQ-UHFFFAOYSA-N 0.000 claims description 2
- NFLVOTHMQAIYAZ-UHFFFAOYSA-N 2-acetyl-n-(4-methylphenyl)sulfonyl-3-oxo-4-phenylbutanamide Chemical compound C=1C=C(C)C=CC=1S(=O)(=O)NC(=O)C(C(=O)C)C(=O)CC1=CC=CC=C1 NFLVOTHMQAIYAZ-UHFFFAOYSA-N 0.000 claims 2
- NDGFPRDBCQWUFS-UHFFFAOYSA-N 2-acetyl-n-(4-methylphenyl)sulfonyl-3-oxobutanamide Chemical compound CC(=O)C(C(C)=O)C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 NDGFPRDBCQWUFS-UHFFFAOYSA-N 0.000 claims 2
- OBEQPUARFBKQQT-UHFFFAOYSA-N 2-benzoyl-n-(4-methylphenyl)sulfonyl-3-oxobutanamide Chemical compound C=1C=CC=CC=1C(=O)C(C(=O)C)C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 OBEQPUARFBKQQT-UHFFFAOYSA-N 0.000 claims 2
- UOFFPNUSJNZNBT-UHFFFAOYSA-N 4,4-dimethyl-n-(4-methylphenyl)sulfonyl-2,6-dioxocyclohexane-1-carboxamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)C1C(=O)CC(C)(C)CC1=O UOFFPNUSJNZNBT-UHFFFAOYSA-N 0.000 claims 2
- HMAHREXOGJKPEC-UHFFFAOYSA-N 4-methyl-n-(4-methylphenyl)sulfonyl-2,6-dioxocyclohexane-1-carboxamide Chemical compound O=C1CC(C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 HMAHREXOGJKPEC-UHFFFAOYSA-N 0.000 claims 2
- SDEMJWNRMQWCQI-UHFFFAOYSA-N 5-butan-2-ylcyclohexane-1,3-dione Chemical compound CCC(C)C1CC(=O)CC(=O)C1 SDEMJWNRMQWCQI-UHFFFAOYSA-N 0.000 claims 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims 2
- FYOURVVFOKJSGV-UHFFFAOYSA-N n-(4-chlorophenyl)sulfonyl-2,6-dioxo-4-propan-2-ylcyclohexane-1-carboxamide Chemical compound O=C1CC(C(C)C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 FYOURVVFOKJSGV-UHFFFAOYSA-N 0.000 claims 2
- IAIUMVPEFJQUIS-UHFFFAOYSA-N n-(4-methylphenyl)sulfonyl-2,4-dioxospiro[5.5]undecane-3-carboxamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)C1C(=O)CC2(CCCCC2)CC1=O IAIUMVPEFJQUIS-UHFFFAOYSA-N 0.000 claims 2
- VFHOQWNTWPSNAW-UHFFFAOYSA-N n-(4-methylphenyl)sulfonyl-2,6-dioxo-4-pentan-3-ylcyclohexane-1-carboxamide Chemical compound O=C1CC(C(CC)CC)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(C)C=C1 VFHOQWNTWPSNAW-UHFFFAOYSA-N 0.000 claims 2
- PGZKYBVFMUYJSZ-UHFFFAOYSA-N n-(benzenesulfonyl)-4,4-dimethyl-2,6-dioxocyclohexane-1-carboxamide Chemical compound O=C1CC(C)(C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=CC=C1 PGZKYBVFMUYJSZ-UHFFFAOYSA-N 0.000 claims 2
- CVBUKMMMRLOKQR-UHFFFAOYSA-N 1-phenylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=C1 CVBUKMMMRLOKQR-UHFFFAOYSA-N 0.000 claims 1
- NROOHYGFTHTDFF-UHFFFAOYSA-N 1-phenylpentane-2,4-dione Chemical compound CC(=O)CC(=O)CC1=CC=CC=C1 NROOHYGFTHTDFF-UHFFFAOYSA-N 0.000 claims 1
- DMIIMPQQPXUKOO-UHFFFAOYSA-N 5-methylcyclohexane-1,3-dione Chemical compound CC1CC(=O)CC(=O)C1 DMIIMPQQPXUKOO-UHFFFAOYSA-N 0.000 claims 1
- RHELOIKNLIFWEO-UHFFFAOYSA-N 5-propylcyclohexane-1,3-dione Chemical compound CCCC1CC(=O)CC(=O)C1 RHELOIKNLIFWEO-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- LKFBIHAJCFDIIN-UHFFFAOYSA-N spiro[5.5]undecane-2,4-dione Chemical compound C1C(=O)CC(=O)CC11CCCCC1 LKFBIHAJCFDIIN-UHFFFAOYSA-N 0.000 claims 1
- 239000008280 blood Substances 0.000 abstract description 16
- 210000004369 blood Anatomy 0.000 abstract description 16
- 230000002218 hypoglycaemic effect Effects 0.000 abstract description 6
- 230000003345 hyperglycaemic effect Effects 0.000 abstract description 5
- 239000000376 reactant Substances 0.000 abstract description 3
- 230000002159 abnormal effect Effects 0.000 abstract description 2
- 150000001260 acyclic compounds Chemical class 0.000 abstract 1
- 125000002015 acyclic group Chemical group 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 63
- 238000004458 analytical method Methods 0.000 description 16
- 239000000460 chlorine Substances 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- -1 sulfonylcarbamoyl Chemical class 0.000 description 5
- 241000124008 Mammalia Species 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 241000700159 Rattus Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 239000012442 inert solvent Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- NWXDGZLXHUHIRT-UHFFFAOYSA-N dimethyl 2-(cyclohexanecarbonylamino)-5,6-dihydro-4h-cyclopenta[b]thiophene-3,4-dicarboxylate Chemical compound COC(=O)C=1C=2C(C(=O)OC)CCC=2SC=1NC(=O)C1CCCCC1 NWXDGZLXHUHIRT-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 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
- 238000002360 preparation method Methods 0.000 description 2
- KKFDJZZADQONDE-UHFFFAOYSA-N (hydridonitrato)hydroxidocarbon(.) Chemical compound O[C]=N KKFDJZZADQONDE-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- PKQIDSVLSKFZQC-UHFFFAOYSA-N 3-oxobutanal Chemical compound CC(=O)CC=O PKQIDSVLSKFZQC-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 241001163743 Perlodes Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229940100389 Sulfonylurea Drugs 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 229940125708 antidiabetic agent Drugs 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000001722 carbon compounds Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Substances ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- NIQQIJXGUZVEBB-UHFFFAOYSA-N methanol;propan-2-one Chemical compound OC.CC(C)=O NIQQIJXGUZVEBB-UHFFFAOYSA-N 0.000 description 1
- LCRKUSTWMGWUFR-UHFFFAOYSA-N n-(4-chlorophenyl)sulfonyl-4,4-dimethyl-2,6-dioxocyclohexane-1-carboxamide;sodium Chemical compound [Na].O=C1CC(C)(C)CC(=O)C1C(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 LCRKUSTWMGWUFR-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/52—Y being a hetero atom
- C07C311/53—X and Y not being nitrogen atoms, e.g. N-sulfonylcarbamic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/51—Y being a hydrogen or a carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US478497A US3917692A (en) | 1974-06-12 | 1974-06-12 | Arylsulfonylcarbamoyl-1,3-dicarbonylalicyclic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1051924A true CA1051924A (fr) | 1979-04-03 |
Family
ID=23900189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA227,783A Expired CA1051924A (fr) | 1974-06-12 | 1975-05-26 | Composes arylsulfonylcarbamoyl dicarbonyl-1,3 alicycliques et arylsulfonylcarbamoyl dicarbonyl-1,3 acycliques |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3917692A (fr) |
| JP (1) | JPS5829785B2 (fr) |
| AU (1) | AU8129175A (fr) |
| BE (1) | BE829953A (fr) |
| CA (1) | CA1051924A (fr) |
| CH (1) | CH596158A5 (fr) |
| DE (1) | DE2526195A1 (fr) |
| DK (1) | DK261775A (fr) |
| FR (1) | FR2274288A1 (fr) |
| GB (1) | GB1454737A (fr) |
| IE (1) | IE41477B1 (fr) |
| LU (1) | LU72697A1 (fr) |
| NL (1) | NL7506830A (fr) |
| SE (1) | SE7506707L (fr) |
| YU (1) | YU40265B (fr) |
| ZA (1) | ZA753689B (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54156826A (en) * | 1978-05-23 | 1979-12-11 | Sumitomo Electric Ind Ltd | Metod of making glass fiber for light transmission |
| US4347380A (en) * | 1979-04-20 | 1982-08-31 | Stauffer Chemical Company | N-Acylsulfonamide herbicidal antidotes |
| US5135941A (en) * | 1989-12-18 | 1992-08-04 | G. D. Searle & Co. | LTB4 synthesis inhibitors |
| AR037097A1 (es) | 2001-10-05 | 2004-10-20 | Novartis Ag | Compuestos acilsulfonamidas, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento |
| WO2004113091A1 (fr) * | 2003-06-24 | 2004-12-29 | Idemitsu Kosan Co., Ltd. | Materiel d'enregistrement thermosensible et derive de benzenesulfonamide |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3298917A (en) * | 1964-09-15 | 1967-01-17 | Merck & Co Inc | Antidiabetic nu-acylaliphaticsulfonamides |
| CH475250A (de) * | 1966-08-25 | 1969-07-15 | Geigy Ag J R | Verfahren zur Herstellung von neuen N'-substituierten N-Arylsulfonylharnstoffen |
-
1974
- 1974-06-12 US US478497A patent/US3917692A/en not_active Expired - Lifetime
-
1975
- 1975-05-16 AU AU81291/75A patent/AU8129175A/en not_active Expired
- 1975-05-26 CA CA227,783A patent/CA1051924A/fr not_active Expired
- 1975-06-06 GB GB2445575A patent/GB1454737A/en not_active Expired
- 1975-06-06 BE BE157097A patent/BE829953A/fr unknown
- 1975-06-09 ZA ZA00753689A patent/ZA753689B/xx unknown
- 1975-06-09 NL NL7506830A patent/NL7506830A/xx unknown
- 1975-06-10 LU LU72697A patent/LU72697A1/xx unknown
- 1975-06-10 DK DK261775A patent/DK261775A/da unknown
- 1975-06-11 SE SE7506707A patent/SE7506707L/xx unknown
- 1975-06-11 CH CH756575A patent/CH596158A5/xx not_active IP Right Cessation
- 1975-06-11 JP JP50069778A patent/JPS5829785B2/ja not_active Expired
- 1975-06-11 IE IE1312/75A patent/IE41477B1/en unknown
- 1975-06-11 FR FR7518300A patent/FR2274288A1/fr active Granted
- 1975-06-12 DE DE19752526195 patent/DE2526195A1/de active Pending
- 1975-06-12 YU YU1515/75A patent/YU40265B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7506830A (nl) | 1975-12-16 |
| FR2274288B1 (fr) | 1978-11-10 |
| FR2274288A1 (fr) | 1976-01-09 |
| YU40265B (en) | 1985-12-31 |
| SE7506707L (sv) | 1975-12-15 |
| LU72697A1 (fr) | 1976-04-13 |
| YU151575A (en) | 1982-06-30 |
| BE829953A (fr) | 1975-12-08 |
| AU8129175A (en) | 1976-11-25 |
| GB1454737A (en) | 1976-11-03 |
| US3917692A (en) | 1975-11-04 |
| DE2526195A1 (de) | 1976-01-02 |
| ZA753689B (en) | 1976-05-26 |
| DK261775A (da) | 1975-12-13 |
| JPS5111734A (fr) | 1976-01-30 |
| CH596158A5 (fr) | 1978-02-28 |
| IE41477L (en) | 1975-12-12 |
| IE41477B1 (en) | 1980-01-16 |
| JPS5829785B2 (ja) | 1983-06-24 |
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