CA2435847A1 - Aniline derivatives useful as phosphodiesterase 4 inhibitors - Google Patents
Aniline derivatives useful as phosphodiesterase 4 inhibitors Download PDFInfo
- Publication number
- CA2435847A1 CA2435847A1 CA002435847A CA2435847A CA2435847A1 CA 2435847 A1 CA2435847 A1 CA 2435847A1 CA 002435847 A CA002435847 A CA 002435847A CA 2435847 A CA2435847 A CA 2435847A CA 2435847 A1 CA2435847 A1 CA 2435847A1
- Authority
- CA
- Canada
- Prior art keywords
- pyridylmethyl
- diphenylamine
- methoxy
- cyclopentyloxy
- substituted
- 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
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 title description 17
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 title 1
- -1 e.g. Chemical class 0.000 claims abstract description 456
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims abstract description 452
- 150000001875 compounds Chemical class 0.000 claims abstract description 189
- 101100296720 Dictyostelium discoideum Pde4 gene Proteins 0.000 claims abstract 2
- 101100082610 Plasmodium falciparum (isolate 3D7) PDEdelta gene Proteins 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims description 217
- 125000004432 carbon atom Chemical group C* 0.000 claims description 181
- 229910052736 halogen Inorganic materials 0.000 claims description 159
- 150000002367 halogens Chemical class 0.000 claims description 151
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 117
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 95
- 125000003545 alkoxy group Chemical group 0.000 claims description 94
- 125000004043 oxo group Chemical group O=* 0.000 claims description 86
- 125000003118 aryl group Chemical group 0.000 claims description 81
- 125000006413 ring segment Chemical group 0.000 claims description 77
- 238000000034 method Methods 0.000 claims description 72
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 68
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 62
- 239000000203 mixture Substances 0.000 claims description 53
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 52
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 47
- 108010081348 HRT1 protein Hairy Chemical group 0.000 claims description 41
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 claims description 41
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical group F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 claims description 40
- 125000001072 heteroaryl group Chemical group 0.000 claims description 39
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 37
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 36
- 125000003282 alkyl amino group Chemical group 0.000 claims description 35
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 34
- 229920006395 saturated elastomer Polymers 0.000 claims description 33
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 31
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 31
- 239000002253 acid Substances 0.000 claims description 28
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 28
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 28
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 26
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 26
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 26
- 125000000623 heterocyclic group Chemical group 0.000 claims description 26
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 25
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 25
- 125000002837 carbocyclic group Chemical group 0.000 claims description 24
- 125000002252 acyl group Chemical group 0.000 claims description 23
- 229910052760 oxygen Inorganic materials 0.000 claims description 23
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 23
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 22
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 21
- 125000004414 alkyl thio group Chemical group 0.000 claims description 21
- 125000005842 heteroatom Chemical group 0.000 claims description 21
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 21
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 20
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 20
- 230000000694 effects Effects 0.000 claims description 20
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 19
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 18
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 18
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 18
- 125000004434 sulfur atom Chemical group 0.000 claims description 18
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 17
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 17
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims description 17
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 16
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 16
- 201000010099 disease Diseases 0.000 claims description 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 14
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 14
- 206010027175 memory impairment Diseases 0.000 claims description 14
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 14
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 claims description 13
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 13
- 229910052801 chlorine Inorganic materials 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 13
- 125000004076 pyridyl group Chemical group 0.000 claims description 13
- 102000004190 Enzymes Human genes 0.000 claims description 12
- 108090000790 Enzymes Proteins 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 12
- 125000000304 alkynyl group Chemical group 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 230000002401 inhibitory effect Effects 0.000 claims description 11
- 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 claims description 11
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 10
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 10
- 125000001624 naphthyl group Chemical group 0.000 claims description 10
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 10
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
- 125000006239 protecting group Chemical group 0.000 claims description 9
- 125000005389 trialkylsiloxy group Chemical group 0.000 claims description 9
- PNIUJOQYAGLPHM-UHFFFAOYSA-N 3-[3-cyclopentyloxy-4-methoxy-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=C(C=CC=2)C(O)=O)C=C1OC1CCCC1 PNIUJOQYAGLPHM-UHFFFAOYSA-N 0.000 claims description 8
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 7
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 7
- 201000000980 schizophrenia Diseases 0.000 claims description 7
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 6
- MYSNBAJHBYMBNT-UHFFFAOYSA-N n-[(3-cyclopentyloxy-4-methoxy-2h-pyridin-3-yl)methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OC1CCCC1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 MYSNBAJHBYMBNT-UHFFFAOYSA-N 0.000 claims description 6
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 6
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 6
- 125000005302 thiazolylmethyl group Chemical group [H]C1=C([H])N=C(S1)C([H])([H])* 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 5
- 239000004305 biphenyl Chemical group 0.000 claims description 5
- 235000010290 biphenyl Nutrition 0.000 claims description 5
- 230000003247 decreasing effect Effects 0.000 claims description 5
- 208000027866 inflammatory disease Diseases 0.000 claims description 5
- 239000008194 pharmaceutical composition Substances 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000000335 thiazolyl group Chemical group 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 208000024827 Alzheimer disease Diseases 0.000 claims description 4
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 4
- 208000010859 Creutzfeldt-Jakob disease Diseases 0.000 claims description 4
- 201000011240 Frontotemporal dementia Diseases 0.000 claims description 4
- 208000023105 Huntington disease Diseases 0.000 claims description 4
- 208000018737 Parkinson disease Diseases 0.000 claims description 4
- 208000000609 Pick Disease of the Brain Diseases 0.000 claims description 4
- 230000000172 allergic effect Effects 0.000 claims description 4
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 4
- 230000019771 cognition Effects 0.000 claims description 4
- 230000007423 decrease Effects 0.000 claims description 4
- 206010019196 Head injury Diseases 0.000 claims description 3
- 206010021143 Hypoxia Diseases 0.000 claims description 3
- 208000006011 Stroke Diseases 0.000 claims description 3
- 208000026935 allergic disease Diseases 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 230000007954 hypoxia Effects 0.000 claims description 3
- 125000003870 2-(1-piperidinyl)ethoxy group Chemical group [*]OC([H])([H])C([H])([H])N1C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- PDQRJBACFQYMCP-UHFFFAOYSA-N 3-pyridin-4-ylbenzamide Chemical compound NC(=O)C1=CC=CC(C=2C=CN=CC=2)=C1 PDQRJBACFQYMCP-UHFFFAOYSA-N 0.000 claims description 2
- 208000005314 Multi-Infarct Dementia Diseases 0.000 claims description 2
- 206010039966 Senile dementia Diseases 0.000 claims description 2
- 201000004810 Vascular dementia Diseases 0.000 claims description 2
- 230000001154 acute effect Effects 0.000 claims description 2
- 230000032683 aging Effects 0.000 claims description 2
- 230000002490 cerebral effect Effects 0.000 claims description 2
- 230000002708 enhancing effect Effects 0.000 claims description 2
- 230000004770 neurodegeneration Effects 0.000 claims description 2
- VTFYMSNCTVOXOQ-UHFFFAOYSA-N 3-[4-methoxy-3-(oxolan-3-yloxy)-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=C(C=CC=2)C(O)=O)C=C1OC1CCOC1 VTFYMSNCTVOXOQ-UHFFFAOYSA-N 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 8
- GDGINHFDZMJRKN-UHFFFAOYSA-N 3-[2-[3-(4-chlorophenyl)propoxy]-4-methoxy-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound C=1C=C(Cl)C=CC=1CCCOC1=CC(OC)=CC=C1N(C=1C=C(C=CC=1)C(O)=O)CC1=CC=CN=C1 GDGINHFDZMJRKN-UHFFFAOYSA-N 0.000 claims 4
- RULLGLRZJAUWJC-UHFFFAOYSA-N 3-[3-(2,3-dihydro-1h-inden-2-yloxy)-4-methoxy-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound C1=C(OC2CC3=CC=CC=C3C2)C(OC)=CC=C1N(C=1C=C(C=CC=1)C(O)=O)CC1=CC=CN=C1 RULLGLRZJAUWJC-UHFFFAOYSA-N 0.000 claims 4
- WNAODSRZKOTLRD-UHFFFAOYSA-N 3-[3-(cyclopropylmethoxy)-4-(difluoromethoxy)-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound OC(=O)C1=CC=CC(N(CC=2C=NC=CC=2)C=2C=C(OCC3CC3)C(OC(F)F)=CC=2)=C1 WNAODSRZKOTLRD-UHFFFAOYSA-N 0.000 claims 4
- UGWWTKUPDVMIAT-UHFFFAOYSA-N 3-[3-(cyclopropylmethoxy)-4-methoxy-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=C(C=CC=2)C(O)=O)C=C1OCC1CC1 UGWWTKUPDVMIAT-UHFFFAOYSA-N 0.000 claims 4
- QDAUEZSAGQJRSN-UHFFFAOYSA-N 3-[3-cyclopentyloxy-4-(difluoromethoxy)-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound OC(=O)C1=CC=CC(N(CC=2C=NC=CC=2)C=2C=C(OC3CCCC3)C(OC(F)F)=CC=2)=C1 QDAUEZSAGQJRSN-UHFFFAOYSA-N 0.000 claims 4
- YQCXOTXOYZMSGT-UHFFFAOYSA-N 3-[4-methoxy-3-(2-methoxyethoxy)-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound C1=C(OC)C(OCCOC)=CC(N(CC=2C=NC=CC=2)C=2C=C(C=CC=2)C(O)=O)=C1 YQCXOTXOYZMSGT-UHFFFAOYSA-N 0.000 claims 4
- XQVMANRSBUNGSR-UHFFFAOYSA-N 4-[3-(cyclopropylmethoxy)-4-methoxy-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=CC(=CC=2)C(O)=O)C=C1OCC1CC1 XQVMANRSBUNGSR-UHFFFAOYSA-N 0.000 claims 4
- PFNVGWKABOYUIG-UHFFFAOYSA-N 4-[3-cyclopentyloxy-4-methoxy-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=CC(=CC=2)C(O)=O)C=C1OC1CCCC1 PFNVGWKABOYUIG-UHFFFAOYSA-N 0.000 claims 4
- LKEMHOKFBVYBFR-VQCQRNETSA-N N-[2-[(3R)-4-(difluoromethoxy)oxolan-3-yl]oxyphenyl]-N-(pyridin-3-ylmethyl)pyridin-3-amine Chemical compound FC(OC1[C@@H](COC1)OC1=C(C=CC=C1)N(CC=1C=NC=CC=1)C=1C=NC=CC=1)F LKEMHOKFBVYBFR-VQCQRNETSA-N 0.000 claims 4
- WZWGSXNVMJZJQG-UHFFFAOYSA-N n-(3-cyclopentyloxy-4-methoxyphenyl)-n-(pyridin-3-ylmethyl)pyridin-3-amine Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=NC=CC=2)C=C1OC1CCCC1 WZWGSXNVMJZJQG-UHFFFAOYSA-N 0.000 claims 4
- KMMWYQNGITYSFV-UHFFFAOYSA-N n-[3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl]-n-(pyridin-3-ylmethyl)pyridin-3-amine Chemical compound FC(F)OC1=CC=C(N(CC=2C=NC=CC=2)C=2C=NC=CC=2)C=C1OCC1CC1 KMMWYQNGITYSFV-UHFFFAOYSA-N 0.000 claims 4
- DCWIRBQULCICSN-UHFFFAOYSA-N n-[3-cyclopentyloxy-4-(difluoromethoxy)phenyl]-n-(pyridin-3-ylmethyl)pyridin-3-amine Chemical compound FC(F)OC1=CC=C(N(CC=2C=NC=CC=2)C=2C=NC=CC=2)C=C1OC1CCCC1 DCWIRBQULCICSN-UHFFFAOYSA-N 0.000 claims 4
- NHUAZXDSSJLSSR-UHFFFAOYSA-N n-[[3,4-bis(difluoromethoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound FC(F)OC1=CC=NCC1(OC(F)F)CN(C=1C=CC=CC=1)C1=CC=CC=C1 NHUAZXDSSJLSSR-UHFFFAOYSA-N 0.000 claims 4
- BOIVZFFQBGEXFX-UHFFFAOYSA-N n-[[4-methoxy-3-(2-pyridin-2-ylethoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OCCC=1N=CC=CC=1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 BOIVZFFQBGEXFX-UHFFFAOYSA-N 0.000 claims 4
- FDJBPHLXAYPMRF-UHFFFAOYSA-N 3-(3-cyclopentyloxy-4-methoxyanilino)benzoic acid Chemical compound C1=C(OC2CCCC2)C(OC)=CC=C1NC1=CC=CC(C(O)=O)=C1 FDJBPHLXAYPMRF-UHFFFAOYSA-N 0.000 claims 3
- OUMUNOWUXDBYMX-UHFFFAOYSA-N n-[[3-(cyclopropylmethoxy)-4-(difluoromethoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound FC(F)OC1=CC=NCC1(OCC1CC1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 OUMUNOWUXDBYMX-UHFFFAOYSA-N 0.000 claims 3
- PNYOYNONRXMNAI-UHFFFAOYSA-N n-[[4-methoxy-3-(3-pyridin-4-ylpropoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OCCCC=1C=CN=CC=1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 PNYOYNONRXMNAI-UHFFFAOYSA-N 0.000 claims 3
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 2
- YYLLQPRULFVNTP-FOIFJWKZSA-N N-[2-[(3R)-4-methoxyoxolan-3-yl]oxyphenyl]-N-(pyridin-3-ylmethyl)pyridin-3-amine Chemical compound COC1[C@@H](COC1)OC1=C(C=CC=C1)N(CC=1C=NC=CC=1)C=1C=NC=CC=1 YYLLQPRULFVNTP-FOIFJWKZSA-N 0.000 claims 2
- 230000037396 body weight Effects 0.000 claims 2
- 125000005343 heterocyclic alkyl group Chemical group 0.000 claims 2
- LEHYXDMZGBGISK-UHFFFAOYSA-N n-(3-cyclopentyloxy-4-methoxyphenyl)-n-(pyridin-3-ylmethyl)isoquinolin-4-amine Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C3=CC=CC=C3C=NC=2)C=C1OC1CCCC1 LEHYXDMZGBGISK-UHFFFAOYSA-N 0.000 claims 2
- VGTXHUFPGAREKA-UHFFFAOYSA-N n-(3-cyclopentyloxy-4-methoxyphenyl)-n-(pyridin-3-ylmethyl)pyridin-2-amine Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2N=CC=CC=2)C=C1OC1CCCC1 VGTXHUFPGAREKA-UHFFFAOYSA-N 0.000 claims 2
- OSNHRDBNKUEDPF-UHFFFAOYSA-N n-(3-cyclopentyloxy-4-methoxyphenyl)-n-(pyridin-3-ylmethyl)pyrimidin-5-amine Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=NC=NC=2)C=C1OC1CCCC1 OSNHRDBNKUEDPF-UHFFFAOYSA-N 0.000 claims 2
- QVHODOMCMPUSNN-UHFFFAOYSA-N n-[[3-(2,3-dihydro-1h-inden-1-yloxy)-4-methoxy-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OC1C2=CC=CC=C2CC1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 QVHODOMCMPUSNN-UHFFFAOYSA-N 0.000 claims 2
- XWVICXGHYZVQSD-UHFFFAOYSA-N n-[[3-(cyclopropylmethoxy)-4-methoxy-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OCC1CC1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 XWVICXGHYZVQSD-UHFFFAOYSA-N 0.000 claims 2
- AWSQSUXLWVZOFC-UHFFFAOYSA-N n-[[3-[2-(4-chlorophenyl)ethenoxy]-4-methoxy-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OC=CC=1C=CC(Cl)=CC=1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 AWSQSUXLWVZOFC-UHFFFAOYSA-N 0.000 claims 2
- UCIWLVLLCTUEAB-UHFFFAOYSA-N n-[[4-methoxy-3-(2-methoxyethoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound C=1C=CC=CC=1N(C=1C=CC=CC=1)CC1(OCCOC)CN=CC=C1OC UCIWLVLLCTUEAB-UHFFFAOYSA-N 0.000 claims 2
- KLXOLDSVEVCINI-UHFFFAOYSA-N n-[[4-methoxy-3-(2-phenoxyethoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OCCOC=1C=CC=CC=1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 KLXOLDSVEVCINI-UHFFFAOYSA-N 0.000 claims 2
- WYJAKPFKKKACLA-UHFFFAOYSA-N n-[[4-methoxy-3-(2-pyridin-4-ylethoxy)-2h-pyridin-3-yl]methyl]-n-phenylaniline Chemical compound COC1=CC=NCC1(OCCC=1C=CN=CC=1)CN(C=1C=CC=CC=1)C1=CC=CC=C1 WYJAKPFKKKACLA-UHFFFAOYSA-N 0.000 claims 2
- 208000015122 neurodegenerative disease Diseases 0.000 claims 2
- GXVCOVKPAQZYDG-UHFFFAOYSA-N 3-[4-methoxy-3-(2-pyridin-2-ylethoxy)-n-(pyridin-3-ylmethyl)anilino]benzoic acid Chemical compound COC1=CC=C(N(CC=2C=NC=CC=2)C=2C=C(C=CC=2)C(O)=O)C=C1OCCC1=CC=CC=N1 GXVCOVKPAQZYDG-UHFFFAOYSA-N 0.000 claims 1
- NUMGOEGYRLDSIO-UHFFFAOYSA-N 3-[tert-butyl(dimethyl)silyl]oxy-4-methoxy-n-(pyridin-3-ylmethyl)aniline Chemical compound C1=C(O[Si](C)(C)C(C)(C)C)C(OC)=CC=C1NCC1=CC=CN=C1 NUMGOEGYRLDSIO-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
- C07C217/88—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
- C07C217/92—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the nitrogen atom of at least one of the amino groups being further bound to a carbon atom of a six-membered aromatic ring
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
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- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/32—Oxygen atoms
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Pulmonology (AREA)
- Psychology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Urology & Nephrology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26265101P | 2001-01-22 | 2001-01-22 | |
US60/262,651 | 2001-01-22 | ||
US26719601P | 2001-02-08 | 2001-02-08 | |
US60/267,196 | 2001-02-08 | ||
US30614001P | 2001-07-19 | 2001-07-19 | |
US60/306,140 | 2001-07-19 | ||
PCT/US2002/001508 WO2002074726A2 (en) | 2001-01-22 | 2002-01-22 | Aniline derivatives useful as phosphodiesterase 4 inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2435847A1 true CA2435847A1 (en) | 2002-09-26 |
Family
ID=27401532
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002435847A Abandoned CA2435847A1 (en) | 2001-01-22 | 2002-01-22 | Aniline derivatives useful as phosphodiesterase 4 inhibitors |
Country Status (24)
Country | Link |
---|---|
EP (1) | EP1353907A2 (no) |
JP (1) | JP4223287B2 (no) |
KR (1) | KR100856622B1 (no) |
CN (1) | CN100378075C (no) |
AU (1) | AU2002303078B2 (no) |
BG (1) | BG108003A (no) |
BR (1) | BR0206943A (no) |
CA (1) | CA2435847A1 (no) |
CL (1) | CL2004001165A1 (no) |
CZ (1) | CZ20031986A3 (no) |
EE (1) | EE05362B1 (no) |
HK (1) | HK1066215A1 (no) |
HR (1) | HRP20030662A2 (no) |
HU (1) | HUP0302793A3 (no) |
IL (1) | IL156958A0 (no) |
MA (1) | MA25996A1 (no) |
MX (1) | MXPA03006519A (no) |
NO (1) | NO329548B1 (no) |
NZ (1) | NZ527081A (no) |
PL (1) | PL373301A1 (no) |
SK (1) | SK9152003A3 (no) |
WO (1) | WO2002074726A2 (no) |
YU (1) | YU57603A (no) |
ZA (1) | ZA200305623B (no) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7153871B2 (en) | 2001-01-22 | 2006-12-26 | Memory Pharmaceuticals Corporation | Phosphodiesterase 4 inhibitors, including aminoindazole and aminobenzofuran analogs |
DK1363876T3 (da) * | 2001-02-14 | 2009-11-30 | Karobio Ab | Glucocorticoidreceptormodulatorer |
US7405230B2 (en) * | 2002-07-19 | 2008-07-29 | Memory Pharmaceuticals Corporation | Phosphodiesterase 4 inhibitors, including N-substituted aniline and diphenylamine analogs |
CA2492911A1 (en) | 2002-07-19 | 2004-01-29 | Memory Pharmaceuticals Corporation | 6-amino-1h-indazole and 4-aminobenzofuran compounds as phosphodiesterase 4 inhibitors |
EP1569908B1 (en) | 2002-11-19 | 2010-09-15 | Memory Pharmaceuticals Corporation | Pyridine n-oxide compounds as phosphodiesterase 4 inhibitors |
US20060040981A1 (en) * | 2002-11-22 | 2006-02-23 | Daniel Dube | Use of phosphodiesterase-4 inhibitors as enhancers of cognition |
MXPA05006463A (es) * | 2002-12-27 | 2005-08-26 | Lundbeck & Co As H | Derivados de 1,2,4-triaminobenceno, utiles para tratar transtornos del sistema nervioso central. |
FR2856595B1 (fr) * | 2003-06-27 | 2008-05-30 | Exonhit Therapeutics Sa | Methodes et compositions pour le traitement de deficits cognitifs. |
MXPA06002521A (es) | 2003-09-05 | 2006-06-20 | Altana Pharma Ag | Uso de inhibidores de pde4 para el tratamiento de diabetes mellitus. |
MY141255A (en) * | 2003-12-11 | 2010-03-31 | Memory Pharm Corp | Phosphodiesterase 4 inhibitors, including n-substituted diarylamine analogs |
RU2392278C2 (ru) | 2004-07-15 | 2010-06-20 | Джапан Тобакко Инк. | Конденсированное производное бензамида и ингибитор активности подтипа 1 рецептора ваниллоида (vr1) |
US20070287716A1 (en) * | 2004-10-28 | 2007-12-13 | Hu Essa H | Pyrimidine and Quinoline Potentiators of Metabotropic Glutamate Receptors |
EA015382B1 (ru) | 2005-03-08 | 2011-08-30 | Никомед Гмбх | Применение рофлумиласта для лечения сахарного диабета типа 2 |
WO2006135828A2 (en) * | 2005-06-10 | 2006-12-21 | Memory Pharmaceuticals Corporation | Trisubstituted amines as phosphodiesterase 4 inhibitors |
AR057455A1 (es) * | 2005-07-22 | 2007-12-05 | Merck & Co Inc | Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica |
US7906508B2 (en) | 2005-12-28 | 2011-03-15 | Japan Tobacco Inc. | 3,4-dihydrobenzoxazine compounds and inhibitors of vanilloid receptor subtype 1 (VRI) activity |
AU2008215948A1 (en) | 2007-02-12 | 2008-08-21 | Merck & Co., Inc. | Piperazine derivatives for treatment of AD and related conditions |
EP2110375A1 (en) * | 2008-04-14 | 2009-10-21 | CHIESI FARMACEUTICI S.p.A. | Phosphodiesterase-4 inhibitors belonging to the tertiary amine class |
EP2291181B9 (en) | 2008-04-18 | 2013-09-11 | University College Dublin National University Of Ireland, Dublin | Captodiamine for the treatment of depression symptoms |
WO2010041449A1 (ja) * | 2008-10-09 | 2010-04-15 | 国立大学法人 岡山大学 | Rxr作動性物質を有効成分とする抗アレルギー剤 |
MX2019008390A (es) * | 2009-06-12 | 2019-09-09 | Abivax | Compuestos utiles para tratar cancer. |
US10253020B2 (en) | 2009-06-12 | 2019-04-09 | Abivax | Compounds for preventing, inhibiting, or treating cancer, AIDS and/or premature aging |
KR101982461B1 (ko) | 2009-06-12 | 2019-05-24 | 아비박스 | 조기 노화, 구체적으로 조로증을 치료하는데 유용한 화합물 |
CA2789663C (en) | 2010-02-12 | 2018-10-02 | Raqualia Pharma Inc. | 5-ht4 receptor agonists for the treatment of dementia |
WO2013118855A1 (ja) | 2012-02-09 | 2013-08-15 | 塩野義製薬株式会社 | 複素環および炭素環誘導体 |
CN102603676B (zh) * | 2012-02-20 | 2014-02-12 | 徐江平 | 一种能避免呕吐反应的磷酸二酯酶4抑制剂 |
JP5959670B2 (ja) * | 2012-03-14 | 2016-08-02 | シノケム・コーポレーションSinochem Corporation | 抗腫瘍薬の調製における置換ジフェニルアミン化合物の使用 |
EP2757161A1 (en) | 2013-01-17 | 2014-07-23 | Splicos | miRNA-124 as a biomarker of viral infection |
HRP20211839T1 (hr) | 2013-07-05 | 2022-03-04 | Abivax | Biciklički spojevi korisni za liječenje bolesti uzrokovanih retrovirusima |
CA2921308A1 (en) | 2013-08-16 | 2015-02-19 | Universiteit Maastricht | Treatment of cognitive impairment with pde4 inhibitor |
EP2974729A1 (en) | 2014-07-17 | 2016-01-20 | Abivax | Quinoline derivatives for use in the treatment of inflammatory diseases |
EP3669873A1 (en) | 2018-12-20 | 2020-06-24 | Abivax | Quinoline derivatives for use ine the traeatment of inflammation diseases |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0700389A1 (en) * | 1993-05-27 | 1996-03-13 | Smithkline Beecham Laboratoires Pharmaceutiques | Anti-arrhythmic n-substituted 3-benzazepines or isoquinolines |
JPH07206789A (ja) * | 1993-09-01 | 1995-08-08 | Taisho Pharmaceut Co Ltd | コンブレタスタチン類縁化合物 |
US5591776A (en) * | 1994-06-24 | 1997-01-07 | Euro-Celtique, S.A. | Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV |
FR2729142A1 (fr) * | 1995-01-06 | 1996-07-12 | Smithkline Beecham Lab | Nouvelles amines heterocycliques, leur procede de preparation et leur utilisation en tant que medicaments et notamment en tant qu'agents anti-arythmiques |
CA2295106C (en) * | 1997-06-24 | 2007-03-13 | Nikken Chemicals Co., Ltd. | 3-anilino-2-cycloalkenone derivatives |
WO2000071129A1 (en) * | 1999-05-21 | 2000-11-30 | Bristol-Myers Squibb Company | Pyrrolotriazine inhibitors of kinases |
DE50011851D1 (de) * | 1999-12-18 | 2006-01-19 | Wella Ag | 2-Aminoalkyl-1,4-diaminobenzol-Derivate und diese Verbindungen enthaltende Färbemittel |
-
2002
- 2002-01-22 CZ CZ20031986A patent/CZ20031986A3/cs unknown
- 2002-01-22 EE EEP200300347A patent/EE05362B1/xx not_active IP Right Cessation
- 2002-01-22 WO PCT/US2002/001508 patent/WO2002074726A2/en active Application Filing
- 2002-01-22 MX MXPA03006519A patent/MXPA03006519A/es active IP Right Grant
- 2002-01-22 CA CA002435847A patent/CA2435847A1/en not_active Abandoned
- 2002-01-22 AU AU2002303078A patent/AU2002303078B2/en not_active Ceased
- 2002-01-22 EP EP02731078A patent/EP1353907A2/en not_active Withdrawn
- 2002-01-22 NZ NZ527081A patent/NZ527081A/xx unknown
- 2002-01-22 HU HU0302793A patent/HUP0302793A3/hu unknown
- 2002-01-22 BR BR0206943-1A patent/BR0206943A/pt not_active Application Discontinuation
- 2002-01-22 PL PL02373301A patent/PL373301A1/xx not_active Application Discontinuation
- 2002-01-22 CN CNB028070100A patent/CN100378075C/zh not_active Expired - Fee Related
- 2002-01-22 JP JP2002573735A patent/JP4223287B2/ja not_active Expired - Fee Related
- 2002-01-22 IL IL15695802A patent/IL156958A0/xx unknown
- 2002-01-22 SK SK915-2003A patent/SK9152003A3/sk unknown
- 2002-01-22 KR KR1020037009624A patent/KR100856622B1/ko not_active IP Right Cessation
- 2002-01-22 YU YU57603A patent/YU57603A/sh unknown
-
2003
- 2003-07-18 BG BG108003A patent/BG108003A/bg unknown
- 2003-07-21 ZA ZA2003/05623A patent/ZA200305623B/en unknown
- 2003-07-21 NO NO20033288A patent/NO329548B1/no not_active IP Right Cessation
- 2003-07-22 MA MA27246A patent/MA25996A1/fr unknown
- 2003-08-20 HR HR20030662A patent/HRP20030662A2/hr not_active Application Discontinuation
-
2004
- 2004-05-20 CL CL200401165A patent/CL2004001165A1/es unknown
- 2004-11-17 HK HK04109061A patent/HK1066215A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
BR0206943A (pt) | 2006-01-24 |
HRP20030662A2 (en) | 2005-06-30 |
CL2004001165A1 (es) | 2005-04-15 |
HUP0302793A2 (hu) | 2003-11-28 |
KR100856622B1 (ko) | 2008-09-03 |
NZ527081A (en) | 2006-03-31 |
EP1353907A2 (en) | 2003-10-22 |
ZA200305623B (en) | 2005-01-26 |
EE200300347A (et) | 2003-12-15 |
PL373301A1 (en) | 2005-08-22 |
CN100378075C (zh) | 2008-04-02 |
YU57603A (sh) | 2006-08-17 |
CZ20031986A3 (cs) | 2003-12-17 |
IL156958A0 (en) | 2004-02-08 |
AU2002303078B2 (en) | 2007-08-30 |
EE05362B1 (et) | 2010-12-15 |
NO329548B1 (no) | 2010-11-08 |
KR20040064606A (ko) | 2004-07-19 |
SK9152003A3 (en) | 2004-04-06 |
WO2002074726A3 (en) | 2003-03-13 |
MA25996A1 (fr) | 2003-12-31 |
JP2005507365A (ja) | 2005-03-17 |
MXPA03006519A (es) | 2004-10-15 |
HUP0302793A3 (en) | 2006-01-30 |
BG108003A (bg) | 2004-09-30 |
WO2002074726A2 (en) | 2002-09-26 |
NO20033288L (no) | 2003-09-22 |
NO20033288D0 (no) | 2003-07-21 |
HK1066215A1 (en) | 2005-03-18 |
JP4223287B2 (ja) | 2009-02-12 |
CN1498211A (zh) | 2004-05-19 |
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Effective date: 20120413 |