CA2461381A1 - Chroman derivatives as 5-hydroxytryptamine-6 ligands - Google Patents
Chroman derivatives as 5-hydroxytryptamine-6 ligands Download PDFInfo
- Publication number
- CA2461381A1 CA2461381A1 CA002461381A CA2461381A CA2461381A1 CA 2461381 A1 CA2461381 A1 CA 2461381A1 CA 002461381 A CA002461381 A CA 002461381A CA 2461381 A CA2461381 A CA 2461381A CA 2461381 A1 CA2461381 A1 CA 2461381A1
- Authority
- CA
- Canada
- Prior art keywords
- methyl
- chromen
- dihydro
- amino
- benzenesulfonamide
- 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.)
- Abandoned
Links
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical class C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 title description 8
- 239000003446 ligand Substances 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 96
- 108091005435 5-HT6 receptors Proteins 0.000 claims abstract description 24
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 11
- -1 cycloheteroalkyl Chemical group 0.000 claims description 38
- 125000001072 heteroaryl group Chemical group 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 23
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 16
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 16
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 13
- 150000001412 amines Chemical class 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 9
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 7
- 210000003169 central nervous system Anatomy 0.000 claims description 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims description 4
- 208000019901 Anxiety disease Diseases 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 208000024827 Alzheimer disease Diseases 0.000 claims description 3
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims description 3
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 3
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 201000000980 schizophrenia Diseases 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000000335 thiazolyl group Chemical group 0.000 claims description 3
- 125000001544 thienyl group Chemical group 0.000 claims description 3
- ILLXJTSTTAHMPW-ZZWBGTBQSA-N 2-bromo-n-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2N(C)S(=O)(=O)C1=CC=CC=C1Br ILLXJTSTTAHMPW-ZZWBGTBQSA-N 0.000 claims description 2
- BIGOYIJVKGTZJZ-HWYAHNCWSA-N 3,4-dimethoxy-n-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C(OC)C(OC)=CC=C1S(=O)(=O)N(C)C1=CC=C(CCC(CN[C@H](C)C=2C=CC=CC=2)O2)C2=C1 BIGOYIJVKGTZJZ-HWYAHNCWSA-N 0.000 claims description 2
- KTOFKMSCCFJWBS-VGOFRKELSA-N 4-amino-n-[(2r)-2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C([C@@H](OC1=C2)CN[C@H](C)C=3C=CC=CC=3)CC1=CC=C2NS(=O)(=O)C1=CC=C(N)C=C1 KTOFKMSCCFJWBS-VGOFRKELSA-N 0.000 claims description 2
- KTOFKMSCCFJWBS-VGSWGCGISA-N 4-amino-n-[(2s)-2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C([C@H](OC1=C2)CN[C@H](C)C=3C=CC=CC=3)CC1=CC=C2NS(=O)(=O)C1=CC=C(N)C=C1 KTOFKMSCCFJWBS-VGSWGCGISA-N 0.000 claims description 2
- KTOFKMSCCFJWBS-PLEWWHCXSA-N 4-amino-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(N)C=C1 KTOFKMSCCFJWBS-PLEWWHCXSA-N 0.000 claims description 2
- DQNREVMJMGBQKN-FKSKYRLFSA-N 4-amino-n-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2N(C)S(=O)(=O)C1=CC=C(N)C=C1 DQNREVMJMGBQKN-FKSKYRLFSA-N 0.000 claims description 2
- GAGWXJUNZJSVLD-UHFFFAOYSA-N 4-chloro-n-[2-[(3-hydroxypropylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C2OC(CNCCCO)CCC2=CC=C1NS(=O)(=O)C1=CC=C(Cl)C=C1 GAGWXJUNZJSVLD-UHFFFAOYSA-N 0.000 claims description 2
- AWIXQIBWRFBSEK-PLEWWHCXSA-N 4-chloro-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(Cl)C=C1 AWIXQIBWRFBSEK-PLEWWHCXSA-N 0.000 claims description 2
- FJNWVEWEYQRAJK-FKSKYRLFSA-N 4-chloro-n-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2N(C)S(=O)(=O)C1=CC=C(Cl)C=C1 FJNWVEWEYQRAJK-FKSKYRLFSA-N 0.000 claims description 2
- NFBZRCOLAVPUJL-UHFFFAOYSA-N 4-fluoro-n-[2-[(3-hydroxypropylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C2OC(CNCCCO)CCC2=CC=C1NS(=O)(=O)C1=CC=C(F)C=C1 NFBZRCOLAVPUJL-UHFFFAOYSA-N 0.000 claims description 2
- ZIOGBNJAFVMADK-FKSKYRLFSA-N 4-methoxy-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=CC(OC)=CC=C1S(=O)(=O)NC1=CC=C(CCC(CN[C@H](C)C=2C=CC=CC=2)O2)C2=C1 ZIOGBNJAFVMADK-FKSKYRLFSA-N 0.000 claims description 2
- WZGAORUXLKNXSB-HWYAHNCWSA-N 4-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(C)C=C1 WZGAORUXLKNXSB-HWYAHNCWSA-N 0.000 claims description 2
- NCELXXSBJZTWHQ-NYRJJRHWSA-N 5-bromo-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]thiophene-2-sulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(Br)S1 NCELXXSBJZTWHQ-NYRJJRHWSA-N 0.000 claims description 2
- FWOQQSYVHAAAIO-FKSKYRLFSA-N 5-chloro-3-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]-1-benzothiophene-2-sulfonamide Chemical compound C1([C@H](NCC2OC3=CC(NS(=O)(=O)C4=C(C5=CC(Cl)=CC=C5S4)C)=CC=C3CC2)C)=CC=CC=C1 FWOQQSYVHAAAIO-FKSKYRLFSA-N 0.000 claims description 2
- ITCPCWOZLJVHMY-NYRJJRHWSA-N 5-chloro-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]thiophene-2-sulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(Cl)S1 ITCPCWOZLJVHMY-NYRJJRHWSA-N 0.000 claims description 2
- YBSRWLPYDCLVSK-QRIPLOBPSA-N 5-chloro-n-methyl-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]thiophene-2-sulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2N(C)S(=O)(=O)C1=CC=C(Cl)S1 YBSRWLPYDCLVSK-QRIPLOBPSA-N 0.000 claims description 2
- YQSSZSAYMFYLAK-NYRJJRHWSA-N 6-chloro-n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]imidazo[2,1-b][1,3]thiazole-5-sulfonamide Chemical compound C1([C@H](NCC2OC3=CC(NS(=O)(=O)C=4N5C=CSC5=NC=4Cl)=CC=C3CC2)C)=CC=CC=C1 YQSSZSAYMFYLAK-NYRJJRHWSA-N 0.000 claims description 2
- 208000019430 Motor disease Diseases 0.000 claims description 2
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 2
- 150000007514 bases Chemical class 0.000 claims description 2
- 208000010877 cognitive disease Diseases 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- ROQBLRJFXQWFLB-XMSQKQJNSA-N n-[(2r)-2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C([C@@H](OC1=C2)CN[C@H](C)C=3C=CC=CC=3)CC1=CC=C2NS(=O)(=O)C1=CC=CC=C1 ROQBLRJFXQWFLB-XMSQKQJNSA-N 0.000 claims description 2
- MPUPRKCXYAKXGG-CJFMBICVSA-N n-[(2r)-2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]naphthalene-1-sulfonamide Chemical compound C1([C@H](NC[C@@H]2OC3=CC(NS(=O)(=O)C=4C5=CC=CC=C5C=CC=4)=CC=C3CC2)C)=CC=CC=C1 MPUPRKCXYAKXGG-CJFMBICVSA-N 0.000 claims description 2
- ROQBLRJFXQWFLB-GCJKJVERSA-N n-[(2s)-2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C([C@H](OC1=C2)CN[C@H](C)C=3C=CC=CC=3)CC1=CC=C2NS(=O)(=O)C1=CC=CC=C1 ROQBLRJFXQWFLB-GCJKJVERSA-N 0.000 claims description 2
- MPUPRKCXYAKXGG-NLFFAJNJSA-N n-[(2s)-2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]naphthalene-1-sulfonamide Chemical compound C1([C@H](NC[C@H]2OC3=CC(NS(=O)(=O)C=4C5=CC=CC=C5C=CC=4)=CC=C3CC2)C)=CC=CC=C1 MPUPRKCXYAKXGG-NLFFAJNJSA-N 0.000 claims description 2
- JUSHGQIHSMKQER-UHFFFAOYSA-N n-[2-(morpholin-4-ylmethyl)-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CN1CCOCC1 JUSHGQIHSMKQER-UHFFFAOYSA-N 0.000 claims description 2
- KNXWOCYAYPNERT-UHFFFAOYSA-N n-[2-(thiomorpholin-4-ylmethyl)-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CN1CCSCC1 KNXWOCYAYPNERT-UHFFFAOYSA-N 0.000 claims description 2
- KQVPFHLRRUPWLC-UHFFFAOYSA-N n-[2-[(1,2-diphenylethylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CNC(C=1C=CC=CC=1)CC1=CC=CC=C1 KQVPFHLRRUPWLC-UHFFFAOYSA-N 0.000 claims description 2
- QDRJYKADDYSPBW-UHFFFAOYSA-N n-[2-[(1,3-benzodioxol-5-ylmethylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=C2CCC(CNCC=3C=C4OCOC4=CC=3)OC2=CC=1NS(=O)(=O)C1=CC=CC=C1 QDRJYKADDYSPBW-UHFFFAOYSA-N 0.000 claims description 2
- ORLIARKOZBWBEA-UHFFFAOYSA-N n-[2-[(2,3-dihydro-1h-inden-1-ylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=C2CCC(CNC3C4=CC=CC=C4CC3)OC2=CC=1NS(=O)(=O)C1=CC=CC=C1 ORLIARKOZBWBEA-UHFFFAOYSA-N 0.000 claims description 2
- XREPGWKDFACLAF-UHFFFAOYSA-N n-[2-[(2,6-dimethylpiperidin-1-yl)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound CC1CCCC(C)N1CC1OC2=CC(NS(=O)(=O)C=3C=CC=CC=3)=CC=C2CC1 XREPGWKDFACLAF-UHFFFAOYSA-N 0.000 claims description 2
- VFBAHPKGBZTJNB-UHFFFAOYSA-N n-[2-[(3-butoxypropylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C2OC(CNCCCOCCCC)CCC2=CC=C1NS(=O)(=O)C1=CC=CC=C1 VFBAHPKGBZTJNB-UHFFFAOYSA-N 0.000 claims description 2
- GVHRPFFOWXVQLX-UHFFFAOYSA-N n-[2-[(3-hydroxypropylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]-4-methoxybenzenesulfonamide Chemical compound C1=CC(OC)=CC=C1S(=O)(=O)NC1=CC=C(CCC(CNCCCO)O2)C2=C1 GVHRPFFOWXVQLX-UHFFFAOYSA-N 0.000 claims description 2
- LYKLVYXZKFKQCL-UHFFFAOYSA-N n-[2-[(3-hydroxypropylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]naphthalene-2-sulfonamide Chemical compound C1=CC=CC2=CC(S(=O)(=O)NC3=CC=C4CCC(OC4=C3)CNCCCO)=CC=C21 LYKLVYXZKFKQCL-UHFFFAOYSA-N 0.000 claims description 2
- NMNLZKVFAIEKKD-UHFFFAOYSA-N n-[2-[(3-phenoxypropylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CNCCCOC1=CC=CC=C1 NMNLZKVFAIEKKD-UHFFFAOYSA-N 0.000 claims description 2
- FQUZKJPVIJUETI-UHFFFAOYSA-N n-[2-[(4-phenylbutan-2-ylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1CC2=CC=C(NS(=O)(=O)C=3C=CC=CC=3)C=C2OC1CNC(C)CCC1=CC=CC=C1 FQUZKJPVIJUETI-UHFFFAOYSA-N 0.000 claims description 2
- HXOIGDPVNAKTPZ-UHFFFAOYSA-N n-[2-[(6-methylheptan-2-ylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C2OC(CNC(C)CCCC(C)C)CCC2=CC=C1NS(=O)(=O)C1=CC=CC=C1 HXOIGDPVNAKTPZ-UHFFFAOYSA-N 0.000 claims description 2
- CRIAMUZXQQEDGS-UHFFFAOYSA-N n-[2-[(benzylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CNCC1=CC=CC=C1 CRIAMUZXQQEDGS-UHFFFAOYSA-N 0.000 claims description 2
- GUOCWZSITCMHCG-UHFFFAOYSA-N n-[2-[(propan-2-ylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C2OC(CNC(C)C)CCC2=CC=C1NS(=O)(=O)C1=CC=CC=C1 GUOCWZSITCMHCG-UHFFFAOYSA-N 0.000 claims description 2
- IJURTMPWEYPMSZ-UHFFFAOYSA-N n-[2-[(pyridin-3-ylmethylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CNCC1=CC=CN=C1 IJURTMPWEYPMSZ-UHFFFAOYSA-N 0.000 claims description 2
- GJXCJBIDAZVKSP-UHFFFAOYSA-N n-[2-[(pyridin-4-ylmethylamino)methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(C=C1O2)=CC=C1CCC2CNCC1=CC=NC=C1 GJXCJBIDAZVKSP-UHFFFAOYSA-N 0.000 claims description 2
- GBKCFXXCHCAHQA-UHFFFAOYSA-N n-[2-[[(1-hydroxy-2-methylpropan-2-yl)amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound C1=C2OC(CNC(C)(CO)C)CCC2=CC=C1NS(=O)(=O)C1=CC=CC=C1 GBKCFXXCHCAHQA-UHFFFAOYSA-N 0.000 claims description 2
- SZTSARCCKVNOPN-UHFFFAOYSA-N n-[2-[[(3-methoxyphenyl)methylamino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound COC1=CC=CC(CNCC2OC3=CC(NS(=O)(=O)C=4C=CC=CC=4)=CC=C3CC2)=C1 SZTSARCCKVNOPN-UHFFFAOYSA-N 0.000 claims description 2
- KSFITRJYLAFIHR-UHFFFAOYSA-N n-[2-[[2-(2-hydroxyethyl)piperidin-1-yl]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound OCCC1CCCCN1CC1OC2=CC(NS(=O)(=O)C=3C=CC=CC=3)=CC=C2CC1 KSFITRJYLAFIHR-UHFFFAOYSA-N 0.000 claims description 2
- IZDZOJUPEPKONT-ZZWBGTBQSA-N n-[2-[[[(1r)-1-cyclohexylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C1CCCCC1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=CC=C1 IZDZOJUPEPKONT-ZZWBGTBQSA-N 0.000 claims description 2
- QLSUJDYZWSBRGE-QRIPLOBPSA-N n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]-2,1,3-benzoxadiazole-4-sulfonamide Chemical compound C1([C@H](NCC2OC3=CC(NS(=O)(=O)C=4C5=NON=C5C=CC=4)=CC=C3CC2)C)=CC=CC=C1 QLSUJDYZWSBRGE-QRIPLOBPSA-N 0.000 claims description 2
- SMXLSSFADRHULS-PLEWWHCXSA-N n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]-4-(trifluoromethoxy)benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(OC(F)(F)F)C=C1 SMXLSSFADRHULS-PLEWWHCXSA-N 0.000 claims description 2
- NDCPPWBMKVPNDX-PLEWWHCXSA-N n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]-4-(trifluoromethyl)benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=C(C(F)(F)F)C=C1 NDCPPWBMKVPNDX-PLEWWHCXSA-N 0.000 claims description 2
- ROQBLRJFXQWFLB-ZZWBGTBQSA-N n-[2-[[[(1r)-1-phenylethyl]amino]methyl]-3,4-dihydro-2h-chromen-7-yl]benzenesulfonamide Chemical compound N([C@H](C)C=1C=CC=CC=1)CC(OC1=C2)CCC1=CC=C2NS(=O)(=O)C1=CC=CC=C1 ROQBLRJFXQWFLB-ZZWBGTBQSA-N 0.000 claims description 2
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Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
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- 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
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Neurosurgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32695701P | 2001-10-04 | 2001-10-04 | |
| US60/326,957 | 2001-10-04 | ||
| PCT/US2002/030955 WO2003029238A1 (en) | 2001-10-04 | 2002-09-30 | Chroman derivatives as 5-hydroxytryptamine-6 ligands |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2461381A1 true CA2461381A1 (en) | 2003-04-10 |
Family
ID=23274503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002461381A Abandoned CA2461381A1 (en) | 2001-10-04 | 2002-09-30 | Chroman derivatives as 5-hydroxytryptamine-6 ligands |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6706757B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1432696A1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2005505586A (cg-RX-API-DMAC7.html) |
| CN (1) | CN1561338A (cg-RX-API-DMAC7.html) |
| BR (1) | BR0213094A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2461381A1 (cg-RX-API-DMAC7.html) |
| MX (1) | MXPA04003087A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2003029238A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US7435837B2 (en) * | 2003-10-24 | 2008-10-14 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
| US20050261347A1 (en) * | 2003-10-24 | 2005-11-24 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
| JP2007536302A (ja) * | 2004-05-05 | 2007-12-13 | エフ．ホフマン−ラ ロシュ アーゲー | ５−ｈｔ６受容体、５−ｈｔ２ａ受容体、又はその両方の調節に有用なアリールスルホニルベンゾジオキサン類 |
| ES2359725T3 (es) * | 2004-09-30 | 2011-05-26 | F. Hoffmann-La Roche Ag | Composiciones y métodos para el tratamiento de trastornos cognitivos. |
| RU2382036C2 (ru) * | 2004-09-30 | 2010-02-20 | Ф.Хоффманн-Ля Рош Аг | Производные бензоксазина и хиноксалина и их применение |
| WO2006040178A1 (en) * | 2004-10-14 | 2006-04-20 | Abbott Gmbh & Co.Kg | Arylsulfonylmethyl or arylsulfonamide substituted aromatic compounds suitable for treating disorders that respond to madulation of the dopamine d3 receptor |
| WO2006066745A1 (en) * | 2004-12-21 | 2006-06-29 | F.Hoffmann-La Roche Ag | Tetralin and indane derivatives and uses thereof |
| RU2396266C2 (ru) * | 2004-12-21 | 2010-08-10 | Ф. Хоффманн-Ля Рош Аг | Производные хромана и их применения при лечении заболеваний цнс |
| EP1831152B1 (en) * | 2004-12-21 | 2008-09-24 | F. Hoffmann-La Roche AG | Tetralin and indane derivatives and uses thereof as 5-ht antagonists |
| JP2008524275A (ja) * | 2004-12-21 | 2008-07-10 | エフ．ホフマン−ラ ロシュ アーゲー | クロマン誘導体及び５−ｈｔレセプターリガンドとしてのそれらの使用 |
| MX2007007558A (es) * | 2004-12-21 | 2007-07-24 | Hoffmann La Roche | Derivados de tetralina y de indano y usos de los mismos. |
| TW200640931A (en) | 2005-02-17 | 2006-12-01 | Wyeth Corp | Cycloalkylfused indole, benzothiophene, benzofuran and indene derivatives |
| TW200716595A (en) * | 2005-04-22 | 2007-05-01 | Wyeth Corp | Chromane and chromene derivatives and uses thereof |
| WO2006116218A1 (en) * | 2005-04-22 | 2006-11-02 | Wyeth | Crystal forms of {[(2r)-7-(2,6-dichlorophenyl)-5-fluoro-2,3-dihydro-1-benzofuran-2-yl]methyl}amine hydrochloride |
| BRPI0610044A2 (pt) * | 2005-04-22 | 2010-05-25 | Wyeth Corp | combinações terapêuticas para o tratamento ou prevenção de depressão |
| AR054363A1 (es) * | 2005-05-23 | 2007-06-20 | Astrazeneca Ab | Compuestos que exhiben actividad moduladora en el receptor 5-hidroxi-triptamina 6 |
| AR054044A1 (es) * | 2005-05-23 | 2007-05-30 | Astrazeneca Ab | Derivados de cromano y tetrahidronaftaleno como moduladores del receptor 5 - ht6; intermediarios en su preparacion; composiciones farmaceuticas que los contienen y su empelo en la fabricacion de medicamentos para el tratamiento de enfermedades del snc y de la obesidad. |
| WO2007051735A1 (en) | 2005-11-03 | 2007-05-10 | F. Hoffmann-La Roche Ag | Arylsulfonylchromans as 5-ht6 inhibitors indolylmaleimide derivatives as protein kinase inhibitors |
| JP2009541249A (ja) * | 2006-06-20 | 2009-11-26 | エフ．ホフマン−ラ ロシュ アーゲー | アリールスルホニルナフタレン誘導体およびその使用 |
| CN101472883A (zh) * | 2006-06-20 | 2009-07-01 | 弗·哈夫曼-拉罗切有限公司 | 芳基磺酰氨基四氢萘衍生物以及其应用 |
| AU2007263084A1 (en) * | 2006-06-20 | 2007-12-27 | F. Hoffmann-La Roche Ag | Tetralin and indane derivatives and uses thereof |
| CL2007003044A1 (es) * | 2006-10-24 | 2008-07-04 | Wyeth Corp | Compuestos derivados de benzoxazina; composicion farmaceutica que los comprende; y uso para el tratamiento de un trastorno psicotico, bipolar, depresivo y abuso o dependencia de sustancias entre otros. |
| TW200831478A (en) * | 2006-10-25 | 2008-08-01 | Wyeth Corp | Chromane derivatives, synthesis thereof, and intermediates thereto |
| US8524766B2 (en) * | 2008-04-29 | 2013-09-03 | Nsab, Filial Af Neurosearch Sweden Ab, Sverige | Modulators of dopamine neurotransmission |
| AU2009242095A1 (en) | 2008-04-29 | 2009-11-05 | Nsab, Filial Af Neurosearch Sweden Ab, Sverige | Modulators of dopamine neurotransmission |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4135474A1 (de) | 1991-10-28 | 1993-04-29 | Bayer Ag | 2-aminomethyl-chromane |
| ATE191716T1 (de) * | 1992-08-17 | 2000-04-15 | Chugai Pharmaceutical Co Ltd | Benzopyran und benzoxazin-derivate |
| US6448269B1 (en) * | 1993-07-22 | 2002-09-10 | Eli Lilly And Company | Glycoprotein IIb/IIIa antagonists |
| GB9316111D0 (en) * | 1993-08-04 | 1993-09-22 | Pfizer Ltd | Benzopyrans |
| SK282402B6 (sk) | 1993-08-19 | 2002-01-07 | Janssen Pharmaceutica N. V. | Deriváty dihydrobenzopyránu, spôsob a medziprodukty na ich výrobu, ich použitie a farmaceutický prostriedok na ich báze |
| US5663194A (en) * | 1995-07-25 | 1997-09-02 | Mewshaw; Richard E. | Chroman-2-ylmethylamino derivatives |
| US6191164B1 (en) * | 1996-05-15 | 2001-02-20 | Hoechst Aktiengesellschaft | Sulfonamide-substituted chromans, processes for their preparation, their use as a medicament or diagnostic, and medicament comprising them |
| PT1027043E (pt) * | 1996-12-10 | 2005-02-28 | Bristol Myers Squibb Co | Benzodioxole benzofurano di-hidrobenzofurano e benzodioxano como agentes melatonergicos |
| US6034256A (en) * | 1997-04-21 | 2000-03-07 | G.D. Searle & Co. | Substituted benzopyran derivatives for the treatment of inflammation |
| US6051586A (en) * | 1997-12-19 | 2000-04-18 | Bayer Corporation | Sulfonamide substituted chroman derivatives useful as beta 3 adrenoreceptor agonists |
| IL136688A0 (en) * | 1997-12-19 | 2001-06-14 | Bayer Ag | Novel sulfonamide substituted chroman derivatives useful as beta-3 adrenoreceptor agonists |
| GB9813949D0 (en) * | 1998-06-29 | 1998-08-26 | Smithkline Beecham Plc | Novel compounds |
| CN1318413C (zh) * | 1998-09-23 | 2007-05-30 | 研究发展基金会 | 生育酚、生育三烯酚、其它苯并二氢吡喃和侧链衍生物,及其用途 |
| FR2787789B1 (fr) * | 1998-12-29 | 2002-06-14 | Lipha | Benzopyranes et benzoxepines utilisables dans le traitement de dyslipidemies, de l'atherosclerose et du diabete, compositions pharmaceutiques les contenant et procedes de preparations |
| SE9902267D0 (sv) | 1999-06-16 | 1999-06-16 | Astra Ab | New compounds |
| ATE309995T1 (de) * | 1999-08-26 | 2005-12-15 | Aventis Pharma Inc | Substituierte (aminoiminomethyl oder aminomethyl) dihydrobenzofurane und benozopyrane |
| EP1212314B1 (en) * | 1999-09-17 | 2005-11-30 | Nissan Chemical Industries, Ltd. | Benzopyran derivative |
| US6323238B1 (en) * | 1999-10-21 | 2001-11-27 | Dongbu Hannong Chemical Co., Ltd. | Benzopyranyl guanidine derivatives, process for preparation thereof, and pharmaceutical compositions containing them |
-
2002
- 2002-09-30 CA CA002461381A patent/CA2461381A1/en not_active Abandoned
- 2002-09-30 BR BR0213094-7A patent/BR0213094A/pt not_active IP Right Cessation
- 2002-09-30 EP EP02800383A patent/EP1432696A1/en not_active Withdrawn
- 2002-09-30 WO PCT/US2002/030955 patent/WO2003029238A1/en not_active Ceased
- 2002-09-30 MX MXPA04003087A patent/MXPA04003087A/es unknown
- 2002-09-30 JP JP2003532487A patent/JP2005505586A/ja active Pending
- 2002-09-30 CN CNA028193342A patent/CN1561338A/zh active Pending
- 2002-10-02 US US10/263,890 patent/US6706757B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2005505586A (ja) | 2005-02-24 |
| US20030158175A1 (en) | 2003-08-21 |
| US6706757B2 (en) | 2004-03-16 |
| EP1432696A1 (en) | 2004-06-30 |
| CN1561338A (zh) | 2005-01-05 |
| WO2003029238A1 (en) | 2003-04-10 |
| MXPA04003087A (es) | 2004-09-06 |
| BR0213094A (pt) | 2004-10-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |