NO317742B1 - Nye heterocykliske forbindelser, fremgangsmate ved deres fremstilling ogfarmasoytiske sammensetninger som inneholder dem, samt anvendelse av forbindelsene for fremstilling av et medikament - Google Patents
Nye heterocykliske forbindelser, fremgangsmate ved deres fremstilling ogfarmasoytiske sammensetninger som inneholder dem, samt anvendelse av forbindelsene for fremstilling av et medikament Download PDFInfo
- Publication number
- NO317742B1 NO317742B1 NO19981814A NO981814A NO317742B1 NO 317742 B1 NO317742 B1 NO 317742B1 NO 19981814 A NO19981814 A NO 19981814A NO 981814 A NO981814 A NO 981814A NO 317742 B1 NO317742 B1 NO 317742B1
- Authority
- NO
- Norway
- Prior art keywords
- formula
- compound
- compounds
- group
- dihydro
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 195
- 238000002360 preparation method Methods 0.000 title claims description 53
- 238000000034 method Methods 0.000 title claims description 50
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 7
- 229940079593 drug Drugs 0.000 title claims description 4
- 239000003814 drug Substances 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title description 7
- 150000002391 heterocyclic compounds Chemical class 0.000 title description 2
- 239000002253 acid Substances 0.000 claims abstract description 32
- 150000003839 salts Chemical class 0.000 claims abstract description 31
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims abstract description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- -1 diastereoisomers Chemical class 0.000 claims abstract description 15
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 13
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 13
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- 125000004385 trihaloalkyl group Chemical group 0.000 claims abstract description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 23
- 150000001412 amines Chemical class 0.000 claims description 18
- 238000011282 treatment Methods 0.000 claims description 15
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 11
- 230000007062 hydrolysis Effects 0.000 claims description 11
- 238000006460 hydrolysis reaction Methods 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 238000000746 purification Methods 0.000 claims description 10
- 230000001193 melatoninergic effect Effects 0.000 claims description 9
- 125000004434 sulfur atom Chemical group 0.000 claims description 8
- 230000029936 alkylation Effects 0.000 claims description 7
- 238000005804 alkylation reaction Methods 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 6
- 150000001540 azides Chemical class 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 4
- 208000035475 disorder Diseases 0.000 claims description 4
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 claims description 4
- IVYHARYOOKCYQZ-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-methylbutanamide Chemical compound O1CCOC2=C1C=CC=C2CCCC(=O)NC IVYHARYOOKCYQZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 3
- 239000007858 starting material Substances 0.000 claims description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 claims description 2
- 150000001263 acyl chlorides Chemical class 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 150000001734 carboxylic acid salts Chemical class 0.000 claims description 2
- 150000008050 dialkyl sulfates Chemical class 0.000 claims description 2
- 238000006698 hydrazinolysis reaction Methods 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 2
- BCPFHPIIZBJGCC-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzoxathiin-5-yl)-n-ethylbutanamide Chemical compound O1CCSC2=C1C=CC=C2CCCC(=O)NCC BCPFHPIIZBJGCC-UHFFFAOYSA-N 0.000 claims 1
- UHYGNCSJJAWXBS-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzoxathiin-5-yl)-n-methylbutanamide Chemical compound O1CCSC2=C1C=CC=C2CCCC(=O)NC UHYGNCSJJAWXBS-UHFFFAOYSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 abstract description 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 5
- 125000003342 alkenyl group Chemical group 0.000 abstract description 4
- HPARLNRMYDSBNO-UHFFFAOYSA-N 1,4-benzodioxine Chemical compound C1=CC=C2OC=COC2=C1 HPARLNRMYDSBNO-UHFFFAOYSA-N 0.000 abstract description 3
- 150000007513 acids Chemical class 0.000 abstract description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- FTEDICXUYBLEMB-UHFFFAOYSA-N 1,2-benzoxathiine Chemical class C1=CC=C2OSC=CC2=C1 FTEDICXUYBLEMB-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 97
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 90
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 64
- 239000000243 solution Substances 0.000 description 48
- 238000002844 melting Methods 0.000 description 41
- 230000008018 melting Effects 0.000 description 41
- 239000000203 mixture Substances 0.000 description 41
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 34
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- 239000000047 product Substances 0.000 description 33
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 27
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
- 239000000377 silicon dioxide Substances 0.000 description 27
- 239000012074 organic phase Substances 0.000 description 26
- 239000002904 solvent Substances 0.000 description 25
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000003921 oil Substances 0.000 description 23
- 235000019198 oils Nutrition 0.000 description 23
- 239000011541 reaction mixture Substances 0.000 description 23
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 21
- 238000003756 stirring Methods 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- 230000002829 reductive effect Effects 0.000 description 20
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 17
- 235000019341 magnesium sulphate Nutrition 0.000 description 17
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000003480 eluent Substances 0.000 description 15
- 238000010992 reflux Methods 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- 150000002148 esters Chemical class 0.000 description 14
- 239000008346 aqueous phase Substances 0.000 description 13
- 239000012230 colorless oil Substances 0.000 description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
- 239000000706 filtrate Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
- 238000001914 filtration Methods 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 239000003153 chemical reaction reagent Substances 0.000 description 9
- 238000001704 evaporation Methods 0.000 description 9
- 230000008020 evaporation Effects 0.000 description 9
- 230000033764 rhythmic process Effects 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 8
- 238000000605 extraction Methods 0.000 description 8
- 150000001408 amides Chemical group 0.000 description 7
- 239000012300 argon atmosphere Substances 0.000 description 7
- 239000000741 silica gel Substances 0.000 description 7
- 229910002027 silica gel Inorganic materials 0.000 description 7
- YJPIGAIKUZMOQA-UHFFFAOYSA-N Melatonin Natural products COC1=CC=C2N(C(C)=O)C=C(CCN)C2=C1 YJPIGAIKUZMOQA-UHFFFAOYSA-N 0.000 description 6
- 102000001419 Melatonin receptor Human genes 0.000 description 6
- 108050009605 Melatonin receptor Proteins 0.000 description 6
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 6
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 150000001299 aldehydes Chemical class 0.000 description 6
- 238000004587 chromatography analysis Methods 0.000 description 6
- 238000003818 flash chromatography Methods 0.000 description 6
- DRLFMBDRBRZALE-UHFFFAOYSA-N melatonin Chemical compound COC1=CC=C2NC=C(CCNC(C)=O)C2=C1 DRLFMBDRBRZALE-UHFFFAOYSA-N 0.000 description 6
- 229960003987 melatonin Drugs 0.000 description 6
- 239000012528 membrane Substances 0.000 description 6
- 230000000144 pharmacologic effect Effects 0.000 description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 description 6
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 5
- 239000012298 atmosphere Substances 0.000 description 5
- XZOWIJDBQIHMFC-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O.CCCC(N)=O XZOWIJDBQIHMFC-UHFFFAOYSA-N 0.000 description 5
- 230000027288 circadian rhythm Effects 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 235000011181 potassium carbonates Nutrition 0.000 description 5
- 208000019116 sleep disease Diseases 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 241001494479 Pecora Species 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- 230000000949 anxiolytic effect Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- 239000006188 syrup Substances 0.000 description 4
- 235000020357 syrup Nutrition 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 208000024827 Alzheimer disease Diseases 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000004694 Eucalyptus leucoxylon Nutrition 0.000 description 3
- 208000019454 Feeding and Eating disease Diseases 0.000 description 3
- 241000287828 Gallus gallus Species 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- 208000008589 Obesity Diseases 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 239000002249 anxiolytic agent Substances 0.000 description 3
- 210000004556 brain Anatomy 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 3
- 230000002060 circadian Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 235000008504 concentrate Nutrition 0.000 description 3
- FCZCIXQGZOUIDN-UHFFFAOYSA-N ethyl 2-diethoxyphosphinothioyloxyacetate Chemical compound CCOC(=O)COP(=S)(OCC)OCC FCZCIXQGZOUIDN-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 206010022437 insomnia Diseases 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 239000012280 lithium aluminium hydride Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- IHPHPGLJYCDONF-UHFFFAOYSA-N n-propylacetamide Chemical compound CCCNC(C)=O IHPHPGLJYCDONF-UHFFFAOYSA-N 0.000 description 3
- 235000020824 obesity Nutrition 0.000 description 3
- 230000007170 pathology Effects 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 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
- LHGVFZTZFXWLCP-UHFFFAOYSA-N pyrocatechol monomethyl ether Natural products COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 3
- 208000012672 seasonal affective disease Diseases 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- JAUFWTSSYRTLLB-UHFFFAOYSA-N (2-phenylacetyl) 2-phenylacetate Chemical compound C=1C=CC=CC=1CC(=O)OC(=O)CC1=CC=CC=C1 JAUFWTSSYRTLLB-UHFFFAOYSA-N 0.000 description 2
- IGXSSRPZRAIXQF-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxin-5-ol Chemical compound O1CCOC2=C1C=CC=C2O IGXSSRPZRAIXQF-UHFFFAOYSA-N 0.000 description 2
- LIQWNOWUUZXEPC-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxine-3-carboxamide Chemical class C1=CC=C2OC(C(=O)N)COC2=C1 LIQWNOWUUZXEPC-UHFFFAOYSA-N 0.000 description 2
- BJXUCBAQZJITKD-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxine-5-carbaldehyde Chemical compound O1CCOC2=C1C=CC=C2C=O BJXUCBAQZJITKD-UHFFFAOYSA-N 0.000 description 2
- GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 description 2
- WPGSNSJXDNFWLM-UHFFFAOYSA-N 2-(2,3-dihydro-1,4-benzodioxin-5-yloxy)ethanamine Chemical compound O1CCOC2=C1C=CC=C2OCCN WPGSNSJXDNFWLM-UHFFFAOYSA-N 0.000 description 2
- YHGKKHMFKFUCMY-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzodioxin-5-yl)butanoic acid Chemical compound O1CCOC2=C1C=CC=C2CCCC(=O)O YHGKKHMFKFUCMY-UHFFFAOYSA-N 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
- UUZNNLAGACPGPQ-UHFFFAOYSA-N 5-(bromomethyl)-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2CBr UUZNNLAGACPGPQ-UHFFFAOYSA-N 0.000 description 2
- CKNVSFHTAJBYOD-UHFFFAOYSA-N 5-methyl-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2C CKNVSFHTAJBYOD-UHFFFAOYSA-N 0.000 description 2
- AAWTVIPAGMUDQL-UHFFFAOYSA-N 8-(2-bromoethoxy)-3,4-dihydro-2h-thiochromene Chemical compound C1CCSC2=C1C=CC=C2OCCBr AAWTVIPAGMUDQL-UHFFFAOYSA-N 0.000 description 2
- 208000027559 Appetite disease Diseases 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 208000019888 Circadian rhythm sleep disease Diseases 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 244000166102 Eucalyptus leucoxylon Species 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
- 208000001456 Jet Lag Syndrome Diseases 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 208000018737 Parkinson disease Diseases 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 230000021736 acetylation Effects 0.000 description 2
- 238000006640 acetylation reaction Methods 0.000 description 2
- 230000000202 analgesic effect Effects 0.000 description 2
- 230000000561 anti-psychotic effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- DVECBJCOGJRVPX-UHFFFAOYSA-N butyryl chloride Chemical compound CCCC(Cl)=O DVECBJCOGJRVPX-UHFFFAOYSA-N 0.000 description 2
- 210000003169 central nervous system Anatomy 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 235000013330 chicken meat Nutrition 0.000 description 2
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 2
- 230000004087 circulation Effects 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000002526 effect on cardiovascular system Effects 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 239000008241 heterogeneous mixture Substances 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 208000033915 jet lag type circadian rhythm sleep disease Diseases 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- NBHLKHCKPPTWFN-UHFFFAOYSA-N n-[2-(2,3-dihydro-1,4-benzodioxin-5-yl)ethyl]acetamide Chemical compound O1CCOC2=C1C=CC=C2CCNC(=O)C NBHLKHCKPPTWFN-UHFFFAOYSA-N 0.000 description 2
- NKCWWGOPWRCYMG-UHFFFAOYSA-N n-[4-(2,3-dihydro-1,4-benzodioxin-5-yl)butyl]acetamide Chemical compound O1CCOC2=C1C=CC=C2CCCCNC(=O)C NKCWWGOPWRCYMG-UHFFFAOYSA-N 0.000 description 2
- 230000016087 ovulation Effects 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- PYNUOAIJIQGACY-UHFFFAOYSA-N propylazanium;chloride Chemical compound Cl.CCCN PYNUOAIJIQGACY-UHFFFAOYSA-N 0.000 description 2
- 102000005962 receptors Human genes 0.000 description 2
- 108020003175 receptors Proteins 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 201000000980 schizophrenia Diseases 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- IIHPVYJPDKJYOU-UHFFFAOYSA-N triphenylcarbethoxymethylenephosphorane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=CC(=O)OCC)C1=CC=CC=C1 IIHPVYJPDKJYOU-UHFFFAOYSA-N 0.000 description 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- ZNOWQGSKZAIRNA-UHFFFAOYSA-N 1-[2-(2,3-dihydro-1,4-benzodioxin-5-yl)ethyl]-3-propylurea Chemical compound O1CCOC2=C1C=CC=C2CCNC(=O)NCCC ZNOWQGSKZAIRNA-UHFFFAOYSA-N 0.000 description 1
- OQURWGJAWSLGQG-UHFFFAOYSA-N 1-isocyanatopropane Chemical compound CCCN=C=O OQURWGJAWSLGQG-UHFFFAOYSA-N 0.000 description 1
- ULDZDSQQHOLKDH-UHFFFAOYSA-N 1-methoxy-2-prop-2-ynoxybenzene Chemical compound COC1=CC=CC=C1OCC#C ULDZDSQQHOLKDH-UHFFFAOYSA-N 0.000 description 1
- LNTVWURFZCEJDN-UHFFFAOYSA-N 1-methylcyclohexa-3,5-diene-1,2-diol Chemical compound CC1(O)C=CC=CC1O LNTVWURFZCEJDN-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- ZYBZYDVRLQSWGG-UHFFFAOYSA-N 2,2-dimethyloct-7-enoic acid Chemical compound OC(=O)C(C)(C)CCCCC=C ZYBZYDVRLQSWGG-UHFFFAOYSA-N 0.000 description 1
- VCLSWKVAHAJSFL-UHFFFAOYSA-N 2,3-dihydro-1,4-benzodioxine-5-carboxylic acid Chemical compound O1CCOC2=C1C=CC=C2C(=O)O VCLSWKVAHAJSFL-UHFFFAOYSA-N 0.000 description 1
- 229940082044 2,3-dihydroxybenzoic acid Drugs 0.000 description 1
- GKAGRAYRWQQHCG-UHFFFAOYSA-N 2-(2,3-dihydro-1,4-benzodioxin-5-yl)acetonitrile Chemical compound O1CCOC2=C1C=CC=C2CC#N GKAGRAYRWQQHCG-UHFFFAOYSA-N 0.000 description 1
- NQAKBMINJHHNDM-UHFFFAOYSA-N 2-(2,3-dihydro-1,4-benzodioxin-5-yl)ethanamine Chemical compound O1CCOC2=C1C=CC=C2CCN NQAKBMINJHHNDM-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- JYYMDCFZUOQGKJ-UHFFFAOYSA-N 2-(3,4-dihydro-2h-thiochromen-8-yloxy)ethanamine Chemical compound C1CCSC2=C1C=CC=C2OCCN JYYMDCFZUOQGKJ-UHFFFAOYSA-N 0.000 description 1
- VJEZYZLITKUTFH-UHFFFAOYSA-N 2-(hydrazinecarbonyl)benzoic acid Chemical compound NNC(=O)C1=CC=CC=C1C(O)=O VJEZYZLITKUTFH-UHFFFAOYSA-N 0.000 description 1
- KCSTXXJTBHIWOQ-UHFFFAOYSA-N 2-[2-(2,3-dihydro-1,4-benzodioxin-5-yloxy)ethyl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CCOC1=CC=CC2=C1OCCO2 KCSTXXJTBHIWOQ-UHFFFAOYSA-N 0.000 description 1
- GQSQTTRREYJDMJ-UHFFFAOYSA-N 2-[3-(2,3-dihydro-1,4-benzodioxin-5-yloxy)propyl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CCCOC1=CC=CC2=C1OCCO2 GQSQTTRREYJDMJ-UHFFFAOYSA-N 0.000 description 1
- GHXXGRNEBPCKEY-UHFFFAOYSA-N 2-[4-(2,3-dihydro-1,4-benzodioxin-5-yloxy)butyl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CCCCOC1=CC=CC2=C1OCCO2 GHXXGRNEBPCKEY-UHFFFAOYSA-N 0.000 description 1
- JMTMSDXUXJISAY-UHFFFAOYSA-N 2H-benzotriazol-4-ol Chemical compound OC1=CC=CC2=C1N=NN2 JMTMSDXUXJISAY-UHFFFAOYSA-N 0.000 description 1
- ONJRTQUWKRDCTA-UHFFFAOYSA-N 2h-thiochromene Chemical compound C1=CC=C2C=CCSC2=C1 ONJRTQUWKRDCTA-UHFFFAOYSA-N 0.000 description 1
- RGGVNXXEMZOMQS-UHFFFAOYSA-N 3,4-dihydro-2h-thiochromen-8-ol Chemical compound C1CCSC2=C1C=CC=C2O RGGVNXXEMZOMQS-UHFFFAOYSA-N 0.000 description 1
- WPWNEKFMGCWNPR-UHFFFAOYSA-N 3,4-dihydro-2h-thiochromene Chemical class C1=CC=C2CCCSC2=C1 WPWNEKFMGCWNPR-UHFFFAOYSA-N 0.000 description 1
- KIWSRIMTLNHPAP-UHFFFAOYSA-N 3-(1,4-benzodioxin-5-yl)propan-1-amine Chemical compound O1C=COC2=C1C=CC=C2CCCN KIWSRIMTLNHPAP-UHFFFAOYSA-N 0.000 description 1
- USRNPKYGIZWLQI-UHFFFAOYSA-N 3-(1,4-benzodioxin-5-yl)propan-1-ol Chemical compound O1C=COC2=C1C=CC=C2CCCO USRNPKYGIZWLQI-UHFFFAOYSA-N 0.000 description 1
- BDPGCDGTQAUPGN-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-methylpropanamide Chemical compound O1CCOC2=C1C=CC=C2CCC(=O)NC BDPGCDGTQAUPGN-UHFFFAOYSA-N 0.000 description 1
- CWYIOWRLAQYLBJ-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzodioxin-5-yl)propanal Chemical compound O1CCOC2=C1C=CC=C2CCC=O CWYIOWRLAQYLBJ-UHFFFAOYSA-N 0.000 description 1
- GHFKRCCBOMTLMF-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzodioxin-5-yl)propanoic acid Chemical compound O1CCOC2=C1C=CC=C2CCC(=O)O GHFKRCCBOMTLMF-UHFFFAOYSA-N 0.000 description 1
- KHLFVQXQOPPTLU-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzodioxin-5-yloxy)propan-1-amine Chemical compound O1CCOC2=C1C=CC=C2OCCCN KHLFVQXQOPPTLU-UHFFFAOYSA-N 0.000 description 1
- CKUDYWHZFVKAPV-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzoxathiin-5-yl)propan-1-amine Chemical compound O1CCSC2=C1C=CC=C2CCCN CKUDYWHZFVKAPV-UHFFFAOYSA-N 0.000 description 1
- VHGXWTVMBQHJJE-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzoxathiin-5-yl)propan-1-ol Chemical compound O1CCSC2=C1C=CC=C2CCCO VHGXWTVMBQHJJE-UHFFFAOYSA-N 0.000 description 1
- KPNWXTGZDBZUDW-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzoxathiin-5-yl)propanal Chemical compound O1CCSC2=C1C=CC=C2CCC=O KPNWXTGZDBZUDW-UHFFFAOYSA-N 0.000 description 1
- HTVPLGXXYUKYGI-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzoxathiin-5-yl)propyl acetate Chemical compound O1CCSC2=C1C=CC=C2CCCOC(=O)C HTVPLGXXYUKYGI-UHFFFAOYSA-N 0.000 description 1
- FXVQNANQKFRUOB-UHFFFAOYSA-N 3-(4,4-dioxo-2,3-dihydro-1,4$l^{6}-benzoxathiin-5-yl)propanoic acid Chemical compound O1CCS(=O)(=O)C2=C1C=CC=C2CCC(=O)O FXVQNANQKFRUOB-UHFFFAOYSA-N 0.000 description 1
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 1
- RMVSBGNAHBQDML-UHFFFAOYSA-N 3-[3-(2,3-dihydro-1,4-benzodioxin-5-yl)propyl]-4-methylbenzenesulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1CCCC1=CC=CC2=C1OCCO2 RMVSBGNAHBQDML-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- XORUODWIOVAEHT-UHFFFAOYSA-N 4-(1,4-benzodioxin-5-yl)-n-methylbutanamide Chemical compound O1C=COC2=C1C=CC=C2CCCC(=O)NC XORUODWIOVAEHT-UHFFFAOYSA-N 0.000 description 1
- QSPVQOYKZPNEAY-UHFFFAOYSA-N 4-(1,4-benzodioxin-5-yl)-n-propylbutanamide Chemical compound O1C=COC2=C1C=CC=C2CCCC(=O)NCCC QSPVQOYKZPNEAY-UHFFFAOYSA-N 0.000 description 1
- XWTIHMGBZIMLBP-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzodioxin-5-yl)butan-1-amine Chemical compound O1CCOC2=C1C=CC=C2CCCCN XWTIHMGBZIMLBP-UHFFFAOYSA-N 0.000 description 1
- JOBCHSHITZNLIS-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzodioxin-5-yl)butanenitrile Chemical compound O1CCOC2=C1C=CC=C2CCCC#N JOBCHSHITZNLIS-UHFFFAOYSA-N 0.000 description 1
- QFKBGLSEVLEOPV-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzodioxin-5-yloxy)butan-1-amine Chemical compound O1CCOC2=C1C=CC=C2OCCCCN QFKBGLSEVLEOPV-UHFFFAOYSA-N 0.000 description 1
- GAGHAWGRMAYWML-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzoxathiin-5-yl)-n-propylbutanamide Chemical compound O1CCSC2=C1C=CC=C2CCCC(=O)NCCC GAGHAWGRMAYWML-UHFFFAOYSA-N 0.000 description 1
- KWFZTJDEZRAKSF-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzoxathiin-5-yl)butan-1-amine Chemical compound O1CCSC2=C1C=CC=C2CCCCN KWFZTJDEZRAKSF-UHFFFAOYSA-N 0.000 description 1
- IXOXHNLMYFOTBR-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzoxathiin-5-yl)butanenitrile Chemical compound O1CCSC2=C1C=CC=C2CCCC#N IXOXHNLMYFOTBR-UHFFFAOYSA-N 0.000 description 1
- NAVFGWPPEPWXIY-UHFFFAOYSA-N 5-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-methylpentanamide Chemical compound O1CCOC2=C1C=CC=C2CCCCC(=O)NC NAVFGWPPEPWXIY-UHFFFAOYSA-N 0.000 description 1
- VWPFPVJSKKNWSG-UHFFFAOYSA-N 5-(2,3-dihydro-1,4-benzoxathiin-5-yl)pentanenitrile Chemical compound O1CCSC2=C1C=CC=C2CCCCC#N VWPFPVJSKKNWSG-UHFFFAOYSA-N 0.000 description 1
- IHXJWHBJQFUJBZ-UHFFFAOYSA-N 5-(2-bromoethoxy)-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2OCCBr IHXJWHBJQFUJBZ-UHFFFAOYSA-N 0.000 description 1
- VXRCSVJLEKTKLY-UHFFFAOYSA-N 5-(3-azidopropyl)-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2CCCN=[N+]=[N-] VXRCSVJLEKTKLY-UHFFFAOYSA-N 0.000 description 1
- YEPRVQAZFGICKQ-UHFFFAOYSA-N 5-(3-bromopropoxy)-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2OCCCBr YEPRVQAZFGICKQ-UHFFFAOYSA-N 0.000 description 1
- KUCDQHRDPXCYHF-UHFFFAOYSA-N 5-(3-bromopropyl)-2,3-dihydro-1,4-benzoxathiine Chemical compound O1CCSC2=C1C=CC=C2CCCBr KUCDQHRDPXCYHF-UHFFFAOYSA-N 0.000 description 1
- KYKHMFKUCWRDHY-UHFFFAOYSA-N 5-(4-bromobutoxy)-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2OCCCCBr KYKHMFKUCWRDHY-UHFFFAOYSA-N 0.000 description 1
- DLMVOXMRGJFYOC-UHFFFAOYSA-N 5-methoxy-2,3-dihydro-1,4-benzodioxine Chemical compound O1CCOC2=C1C=CC=C2OC DLMVOXMRGJFYOC-UHFFFAOYSA-N 0.000 description 1
- RETVOONTWYFZIS-UHFFFAOYSA-N 8-methoxy-2h-chromene Chemical compound C1=CCOC2=C1C=CC=C2OC RETVOONTWYFZIS-UHFFFAOYSA-N 0.000 description 1
- FSCZYYONSDTBCW-UHFFFAOYSA-N 8-methoxy-3,4-dihydro-2h-chromene Chemical compound C1CCOC2=C1C=CC=C2OC FSCZYYONSDTBCW-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- 208000000044 Amnesia Diseases 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 description 1
- 229910014585 C2-Ce Inorganic materials 0.000 description 1
- LSPHULWDVZXLIL-UHFFFAOYSA-N Camphoric acid Natural products CC1(C)C(C(O)=O)CCC1(C)C(O)=O LSPHULWDVZXLIL-UHFFFAOYSA-N 0.000 description 1
- 241000255930 Chironomidae Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 206010052804 Drug tolerance Diseases 0.000 description 1
- 208000030814 Eating disease Diseases 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- 241001248537 Eurema daira Species 0.000 description 1
- 241000287826 Gallus Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 102100024930 Melatonin receptor type 1A Human genes 0.000 description 1
- 101710098568 Melatonin receptor type 1A Proteins 0.000 description 1
- 102100024970 Melatonin receptor type 1B Human genes 0.000 description 1
- 101710098567 Melatonin receptor type 1B Proteins 0.000 description 1
- 208000026139 Memory disease Diseases 0.000 description 1
- 208000019695 Migraine disease Diseases 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- 206010033664 Panic attack Diseases 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 208000028017 Psychotic disease Diseases 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 206010039966 Senile dementia Diseases 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
- 238000007239 Wittig reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 231100000215 acute (single dose) toxicity testing Toxicity 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 108010069175 acyl-CoA transferase Proteins 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 230000003288 anthiarrhythmic effect Effects 0.000 description 1
- 239000000935 antidepressant agent Substances 0.000 description 1
- 229940005513 antidepressants Drugs 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 229940005530 anxiolytics Drugs 0.000 description 1
- 230000006793 arrhythmia Effects 0.000 description 1
- 206010003119 arrhythmia Diseases 0.000 description 1
- 208000011775 arteriosclerosis disease Diseases 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- LSPHULWDVZXLIL-QUBYGPBYSA-N camphoric acid Chemical compound CC1(C)[C@H](C(O)=O)CC[C@]1(C)C(O)=O LSPHULWDVZXLIL-QUBYGPBYSA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- BJUPKWZTXRXARN-UHFFFAOYSA-N carbamic acid;2,3-dihydro-1,4-benzodioxine Chemical class NC(O)=O.C1=CC=C2OCCOC2=C1 BJUPKWZTXRXARN-UHFFFAOYSA-N 0.000 description 1
- 150000003857 carboxamides Chemical group 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- VEZNCHDBSQWUHQ-UHFFFAOYSA-N chlorocyclopropane Chemical compound ClC1CC1 VEZNCHDBSQWUHQ-UHFFFAOYSA-N 0.000 description 1
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 description 1
- 230000008632 circadian clock Effects 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 description 1
- JOHUAELJNSBTGS-UHFFFAOYSA-N cyclohexanecarbonyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC(=O)C1CCCCC1 JOHUAELJNSBTGS-UHFFFAOYSA-N 0.000 description 1
- LZEPOJMTQYNFTR-UHFFFAOYSA-N cyclopropanecarbonyl cyclopropanecarboxylate Chemical compound C1CC1C(=O)OC(=O)C1CC1 LZEPOJMTQYNFTR-UHFFFAOYSA-N 0.000 description 1
- 238000006264 debenzylation reaction Methods 0.000 description 1
- 230000017858 demethylation Effects 0.000 description 1
- 238000010520 demethylation reaction Methods 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 235000014632 disordered eating Nutrition 0.000 description 1
- 239000003210 dopamine receptor blocking agent Substances 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 239000012039 electrophile Substances 0.000 description 1
- 230000007368 endocrine function Effects 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- BKAZEGHEENQRLU-UHFFFAOYSA-N ethyl 3-(1,4-benzodioxin-5-yl)prop-2-enoate Chemical compound O1C=COC2=C1C=CC=C2C=CC(=O)OCC BKAZEGHEENQRLU-UHFFFAOYSA-N 0.000 description 1
- IVFMTIFWVBUMTK-UHFFFAOYSA-N ethyl 5-(2,3-dihydro-1,4-benzodioxin-5-yl)pentanoate Chemical compound O1CCOC2=C1C=CC=C2CCCCC(=O)OCC IVFMTIFWVBUMTK-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 229960001867 guaiacol Drugs 0.000 description 1
- 230000026781 habituation Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 1
- 230000002519 immonomodulatory effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000006742 locomotor activity Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000013289 male long evans rat Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000006984 memory degeneration Effects 0.000 description 1
- 208000023060 memory loss Diseases 0.000 description 1
- BRMYZIKAHFEUFJ-UHFFFAOYSA-L mercury diacetate Chemical compound CC(=O)O[Hg]OC(C)=O BRMYZIKAHFEUFJ-UHFFFAOYSA-L 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- JXAVBMJJVLXKCZ-UHFFFAOYSA-N methyl 1,4-benzodioxine-5-carboxylate Chemical compound O1C=COC2=C1C=CC=C2C(=O)OC JXAVBMJJVLXKCZ-UHFFFAOYSA-N 0.000 description 1
- ZPKXULSJPDNOJY-UHFFFAOYSA-N methyl 2,3-dihydro-1,4-benzodioxine-5-carboxylate Chemical compound O1CCOC2=C1C=CC=C2C(=O)OC ZPKXULSJPDNOJY-UHFFFAOYSA-N 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 230000004089 microcirculation Effects 0.000 description 1
- 206010027599 migraine Diseases 0.000 description 1
- AKXHOSGGEMFKSG-UHFFFAOYSA-N n-(2,3-dihydro-1,4-benzodioxin-5-ylmethyl)acetamide Chemical compound O1CCOC2=C1C=CC=C2CNC(=O)C AKXHOSGGEMFKSG-UHFFFAOYSA-N 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- GCKCHDABYAZHOF-UHFFFAOYSA-N n-[2-(2,3-dihydro-1,4-benzodioxin-5-yloxy)ethyl]-2-phenylacetamide Chemical compound C=1C=CC=2OCCOC=2C=1OCCNC(=O)CC1=CC=CC=C1 GCKCHDABYAZHOF-UHFFFAOYSA-N 0.000 description 1
- BNDIUJAGIVERMC-UHFFFAOYSA-N n-[2-(2,3-dihydro-1,4-benzodioxin-5-yloxy)ethyl]acetamide Chemical compound O1CCOC2=C1C=CC=C2OCCNC(=O)C BNDIUJAGIVERMC-UHFFFAOYSA-N 0.000 description 1
- PMDRGRCKBXERTK-UHFFFAOYSA-N n-[2-(2,3-dihydro-1,4-benzodioxin-5-yloxy)ethyl]cyclopropanecarboxamide Chemical compound C=1C=CC=2OCCOC=2C=1OCCNC(=O)C1CC1 PMDRGRCKBXERTK-UHFFFAOYSA-N 0.000 description 1
- WOQKSFCHMVOHQO-UHFFFAOYSA-N n-[3-(1,4-benzodioxin-5-yl)propyl]acetamide Chemical compound O1C=COC2=C1C=CC=C2CCCNC(=O)C WOQKSFCHMVOHQO-UHFFFAOYSA-N 0.000 description 1
- QCCAVVMJRQQGHM-UHFFFAOYSA-N n-[3-(2,3-dihydro-1,4-benzodioxin-5-yl)propyl]acetamide Chemical compound O1CCOC2=C1C=CC=C2CCCNC(=O)C QCCAVVMJRQQGHM-UHFFFAOYSA-N 0.000 description 1
- DVPDMESGNBGBDB-UHFFFAOYSA-N n-[3-(2,3-dihydro-1,4-benzodioxin-5-yl)propyl]butanamide Chemical compound O1CCOC2=C1C=CC=C2CCCNC(=O)CCC DVPDMESGNBGBDB-UHFFFAOYSA-N 0.000 description 1
- NEXLIMIAVCMETM-UHFFFAOYSA-N n-[3-(3-benzyl-1,4-benzodioxin-5-yl)propyl]acetamide Chemical compound O1C=2C(CCCNC(=O)C)=CC=CC=2OC=C1CC1=CC=CC=C1 NEXLIMIAVCMETM-UHFFFAOYSA-N 0.000 description 1
- RXTUSFOSRQRLDJ-UHFFFAOYSA-N n-[4-(2,3-dihydro-1,4-benzodioxin-5-yl)butyl]but-3-enamide Chemical compound O1CCOC2=C1C=CC=C2CCCCNC(=O)CC=C RXTUSFOSRQRLDJ-UHFFFAOYSA-N 0.000 description 1
- ZWXPAUSMQZPMPS-UHFFFAOYSA-N n-benzyl-5-(2,3-dihydro-1,4-benzodioxin-5-yl)pentanamide Chemical compound C=1C=CC=2OCCOC=2C=1CCCCC(=O)NCC1=CC=CC=C1 ZWXPAUSMQZPMPS-UHFFFAOYSA-N 0.000 description 1
- ODHIEYUXVHANFI-UHFFFAOYSA-N n-cyclobutyl-4-(2,3-dihydro-1,4-benzodioxin-5-yl)butanamide Chemical compound C=1C=CC=2OCCOC=2C=1CCCC(=O)NC1CCC1 ODHIEYUXVHANFI-UHFFFAOYSA-N 0.000 description 1
- AEYWPRODWLOEFK-UHFFFAOYSA-N n-methylmethanamine;pyridine Chemical compound CNC.C1=CC=NC=C1 AEYWPRODWLOEFK-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 208000019906 panic disease Diseases 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 125000005543 phthalimide group Chemical group 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- FYRHIOVKTDQVFC-UHFFFAOYSA-M potassium phthalimide Chemical compound [K+].C1=CC=C2C(=O)[N-]C(=O)C2=C1 FYRHIOVKTDQVFC-UHFFFAOYSA-M 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- WPZSAUFQHYFIPG-UHFFFAOYSA-N propanethioamide Chemical compound CCC(N)=S WPZSAUFQHYFIPG-UHFFFAOYSA-N 0.000 description 1
- YORCIIVHUBAYBQ-UHFFFAOYSA-N propargyl bromide Chemical compound BrCC#C YORCIIVHUBAYBQ-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 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
- 229940107700 pyruvic acid Drugs 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical class [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical class [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000006190 sub-lingual tablet Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 238000007070 tosylation reaction Methods 0.000 description 1
- 239000003558 transferase inhibitor Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/04—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D335/06—Benzothiopyrans; Hydrogenated benzothiopyrans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C07D311/64—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with oxygen atoms directly attached in position 8
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/06—Six-membered rings
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Child & Adolescent Psychology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pyrane Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9705110A FR2762598A1 (fr) | 1997-04-25 | 1997-04-25 | Nouveaux composes heterocycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennnent |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO981814D0 NO981814D0 (no) | 1998-04-22 |
| NO981814L NO981814L (no) | 1998-10-26 |
| NO317742B1 true NO317742B1 (no) | 2004-12-13 |
Family
ID=9506306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19981814A NO317742B1 (no) | 1997-04-25 | 1998-04-22 | Nye heterocykliske forbindelser, fremgangsmate ved deres fremstilling ogfarmasoytiske sammensetninger som inneholder dem, samt anvendelse av forbindelsene for fremstilling av et medikament |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US5919814A (hu) |
| EP (1) | EP0873993B1 (hu) |
| JP (1) | JP4125418B2 (hu) |
| CN (1) | CN1145622C (hu) |
| AT (1) | ATE213496T1 (hu) |
| AU (1) | AU736716B2 (hu) |
| BR (1) | BR9801448B1 (hu) |
| CA (1) | CA2235421C (hu) |
| DE (1) | DE69803894T2 (hu) |
| DK (1) | DK0873993T3 (hu) |
| ES (1) | ES2173556T3 (hu) |
| FR (1) | FR2762598A1 (hu) |
| HK (1) | HK1014956A1 (hu) |
| HU (1) | HU223468B1 (hu) |
| NO (1) | NO317742B1 (hu) |
| NZ (1) | NZ330279A (hu) |
| PL (1) | PL198572B1 (hu) |
| PT (1) | PT873993E (hu) |
| ZA (1) | ZA983490B (hu) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19548708A1 (de) * | 1995-12-23 | 1997-06-26 | Merck Patent Gmbh | Cyclische Sulfone |
| FR2799757B1 (fr) * | 1999-10-15 | 2001-12-14 | Adir | Nouveaux derives polycycliques azaindoliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR2805993B1 (fr) * | 2000-03-08 | 2004-01-16 | Adir | Utilisation de ligands melatoninergiques pour l'obtention de compositions pharmaceutiques destinees a la prevention ou au traitement du developpement de la tolerance aux composes nitres |
| EP1328522A2 (en) * | 2000-10-19 | 2003-07-23 | Merck & Co., Inc. | Estrogen receptor modulators |
| US6750213B2 (en) | 2000-10-19 | 2004-06-15 | Merck & Co., Inc. | Estrogen receptor modulators |
| CN100546992C (zh) * | 2001-10-04 | 2009-10-07 | 旭瑞达有限公司 | 羟基封端的低聚膦酸酯 |
| JP4554219B2 (ja) | 2002-04-24 | 2010-09-29 | メルク・シャープ・エンド・ドーム・コーポレイション | エストロゲン受容体調節剤 |
| FR2918372B1 (fr) * | 2007-07-02 | 2009-08-28 | Servier Lab | Nouveaux derives naphtaleniques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR2918370B1 (fr) * | 2007-07-02 | 2009-08-28 | Servier Lab | Nouveaux derives naphtaleniques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3737195A1 (de) * | 1987-11-03 | 1989-05-18 | Bayer Ag | Chromanderivate, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
| FR2691149B1 (fr) * | 1992-05-18 | 1994-07-08 | Adir | Nouveaux composes thiochromaniques, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent. |
| FR2716680B1 (fr) * | 1994-02-25 | 1996-04-05 | Adir | Nouveaux dérivés de benzodioxane, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent. |
-
1997
- 1997-04-25 FR FR9705110A patent/FR2762598A1/fr not_active Withdrawn
-
1998
- 1998-04-20 CA CA002235421A patent/CA2235421C/fr not_active Expired - Fee Related
- 1998-04-22 NO NO19981814A patent/NO317742B1/no unknown
- 1998-04-23 EP EP98400987A patent/EP0873993B1/fr not_active Expired - Lifetime
- 1998-04-23 PT PT98400987T patent/PT873993E/pt unknown
- 1998-04-23 AT AT98400987T patent/ATE213496T1/de not_active IP Right Cessation
- 1998-04-23 ES ES98400987T patent/ES2173556T3/es not_active Expired - Lifetime
- 1998-04-23 DK DK98400987T patent/DK0873993T3/da active
- 1998-04-23 DE DE69803894T patent/DE69803894T2/de not_active Expired - Fee Related
- 1998-04-24 BR BRPI9801448-0A patent/BR9801448B1/pt not_active IP Right Cessation
- 1998-04-24 PL PL325989A patent/PL198572B1/pl unknown
- 1998-04-24 HU HU9800964A patent/HU223468B1/hu not_active IP Right Cessation
- 1998-04-24 US US09/066,235 patent/US5919814A/en not_active Expired - Fee Related
- 1998-04-24 JP JP11497998A patent/JP4125418B2/ja not_active Expired - Fee Related
- 1998-04-24 NZ NZ330279A patent/NZ330279A/en unknown
- 1998-04-24 AU AU63591/98A patent/AU736716B2/en not_active Ceased
- 1998-04-24 CN CNB981073328A patent/CN1145622C/zh not_active Expired - Fee Related
- 1998-04-24 ZA ZA983490A patent/ZA983490B/xx unknown
-
1999
- 1999-01-14 HK HK99100203A patent/HK1014956A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2762598A1 (fr) | 1998-10-30 |
| HUP9800964A2 (hu) | 2000-05-28 |
| HU223468B1 (hu) | 2004-07-28 |
| NO981814D0 (no) | 1998-04-22 |
| JPH10298178A (ja) | 1998-11-10 |
| CA2235421C (fr) | 2003-09-16 |
| ATE213496T1 (de) | 2002-03-15 |
| ES2173556T3 (es) | 2002-10-16 |
| BR9801448A (pt) | 2000-02-08 |
| JP4125418B2 (ja) | 2008-07-30 |
| CN1145622C (zh) | 2004-04-14 |
| BR9801448B1 (pt) | 2009-01-13 |
| HUP9800964A3 (en) | 2000-06-28 |
| HK1014956A1 (en) | 1999-10-08 |
| EP0873993A1 (fr) | 1998-10-28 |
| AU6359198A (en) | 1998-10-29 |
| HU9800964D0 (en) | 1998-06-29 |
| PL198572B1 (pl) | 2008-06-30 |
| DE69803894T2 (de) | 2002-11-07 |
| CA2235421A1 (fr) | 1998-10-25 |
| DE69803894D1 (de) | 2002-03-28 |
| EP0873993B1 (fr) | 2002-02-20 |
| ZA983490B (en) | 1998-10-29 |
| NO981814L (no) | 1998-10-26 |
| PT873993E (pt) | 2002-07-31 |
| PL325989A1 (en) | 1998-10-26 |
| DK0873993T3 (da) | 2002-06-10 |
| US5919814A (en) | 1999-07-06 |
| NZ330279A (en) | 1998-11-25 |
| CN1197797A (zh) | 1998-11-04 |
| AU736716B2 (en) | 2001-08-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO310654B1 (no) | Nye aryl(alkyl)propylamider, fremgangsmåte ved deres fremstilling og farmasöytiske sammensetninger inneholdende dem | |
| NO310652B1 (no) | Nye alkoksyarylforbindelser, fremgangsmåte ved deres fremstilling og farmasöytiske sammensetninger inneholdende dem | |
| NO317742B1 (no) | Nye heterocykliske forbindelser, fremgangsmate ved deres fremstilling ogfarmasoytiske sammensetninger som inneholder dem, samt anvendelse av forbindelsene for fremstilling av et medikament | |
| AU741753B2 (en) | Substituted heterocyclic compounds, method for preparing and compositions containing same | |
| EP0745584B1 (fr) | Composés arylalkyl(thio) carboxamides ayant une affinité pour des récepteurs mélatoninergiques, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent | |
| AU755115B2 (en) | New cyclic compounds having a cycloalkylene chain, a process for their preparation and pharmaceutical compositions containing them | |
| US6147110A (en) | Heterocyclic compounds | |
| AU2007310769B2 (en) | Novel indole derivatives, process for the preparation thereof and pharmaceutical compositions containing them | |
| EA012283B1 (ru) | Новые соединения нафталина, способ их получения и фармацевтические композиции, содержащие их | |
| NO327107B1 (no) | Nye isokinolinforbindelser, fremgangsmate for deres fremstilling og farmasoytiske sammensetninger inneholdende dem | |
| KR100491601B1 (ko) | 치환된 (디하이드로)벤즈옥사진 및(디하이드로)벤조티아진 화합물, 이들의 제조 방법 및이들을 함유하는 약제학적 조성물 | |
| JP2004518627A (ja) | 置換ビフェニル誘導体、その製造方法およびそれを含有する医薬組成物 | |
| MXPA99009283A (en) | Cyclic derivatives with a cycloalkylenic chain, process for their preparation and pharmaceutical compositions containing them |