AU2003268512A1 - Hydroxy alkyl substituted 1,3,8-triazaspiro[4.5]decan-4-one derivatives useful for the treatment of ORL-1 receptor mediated disorders - Google Patents

Info

Publication number

AU2003268512A1

AU2003268512A1 AU2003268512A AU2003268512A AU2003268512A1 AU 2003268512 A1 AU2003268512 A1 AU 2003268512A1 AU 2003268512 A AU2003268512 A AU 2003268512A AU 2003268512 A AU2003268512 A AU 2003268512A AU 2003268512 A1 AU2003268512 A1 AU 2003268512A1

Authority

AU

Australia

Prior art keywords

group

phenyl

methyl

alkyl

hydroxy

Prior art date

2002-09-09

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

• Espacenet
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• 108010020615 nociceptin receptor Proteins 0.000 title claims description 32
• 230000001404 mediated effect Effects 0.000 title claims description 14
• 150000008631 1,3,8-triazaspiro[4.5]decan-4-ones Chemical class 0.000 title description 5
• 125000002768 hydroxyalkyl group Chemical group 0.000 title description 3
• -1 hydroxy, carboxy Chemical group 0.000 claims description 1182
• 150000001875 compounds Chemical class 0.000 claims description 443
• 125000000217 alkyl group Chemical group 0.000 claims description 163
• 125000001072 heteroaryl group Chemical group 0.000 claims description 138
• 125000001424 substituent group Chemical group 0.000 claims description 133
• 125000003118 aryl group Chemical group 0.000 claims description 121
• 238000000034 method Methods 0.000 claims description 100
• 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 97
• 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 97
• 229910052739 hydrogen Inorganic materials 0.000 claims description 94
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 85
• 239000001257 hydrogen Substances 0.000 claims description 73
• 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 71
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 71
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 70
• 229910052736 halogen Inorganic materials 0.000 claims description 69
• 150000002367 halogens Chemical class 0.000 claims description 69
• 229910052757 nitrogen Inorganic materials 0.000 claims description 66
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 64
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 63
• 101100537937 Caenorhabditis elegans arc-1 gene Proteins 0.000 claims description 58
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 58
• 150000002431 hydrogen Chemical group 0.000 claims description 56
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 56
• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 52
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 50
• 125000004452 carbocyclyl group Chemical group 0.000 claims description 49
• 239000000203 mixture Substances 0.000 claims description 44
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 34
• 150000003839 salts Chemical class 0.000 claims description 32
• 125000003545 alkoxy group Chemical group 0.000 claims description 30
• 230000008569 process Effects 0.000 claims description 28
• 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims description 27
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 27
• 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 26
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 26
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 23
• 208000002193 Pain Diseases 0.000 claims description 22
• 229910052799 carbon Inorganic materials 0.000 claims description 22
• 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 21
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 21
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 21
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 21
• 208000035475 disorder Diseases 0.000 claims description 20
• 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 18
• 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 18
• 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 claims description 17
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 17
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 16
• 239000003814 drug Substances 0.000 claims description 16
• 125000006509 3,4-difluorobenzyl group Chemical group [H]C1=C(F)C(F)=C([H])C(=C1[H])C([H])([H])* 0.000 claims description 15
• 238000002360 preparation method Methods 0.000 claims description 14
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 14
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
• 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 13
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 13
• 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims description 12
• 125000006181 4-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])C([H])([H])* 0.000 claims description 12
• 125000003342 alkenyl group Chemical group 0.000 claims description 12
• 125000002927 2-methoxybenzyl group Chemical group [H]C1=C([H])C([H])=C(C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims description 11
• 125000006180 3-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1[H])C([H])([H])[H])C([H])([H])* 0.000 claims description 11
• 125000006281 4-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Br)C([H])([H])* 0.000 claims description 11
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 11
• 208000019901 Anxiety disease Diseases 0.000 claims description 11
• 208000019695 Migraine disease Diseases 0.000 claims description 11
• 230000036506 anxiety Effects 0.000 claims description 11
• 125000001153 fluoro group Chemical group F* 0.000 claims description 11
• 206010027599 migraine Diseases 0.000 claims description 11
• 239000008194 pharmaceutical composition Substances 0.000 claims description 11
• 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 11
• 125000006507 2,4-difluorobenzyl group Chemical group [H]C1=C(F)C([H])=C(F)C(=C1[H])C([H])([H])* 0.000 claims description 10
• 125000006280 2-bromobenzyl group Chemical group [H]C1=C([H])C(Br)=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
• 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
• 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 10
• 125000006479 2-pyridyl methyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims description 10
• 125000006494 2-trifluoromethyl benzyl group Chemical group [H]C1=C([H])C([H])=C(C(=C1[H])C([H])([H])*)C(F)(F)F 0.000 claims description 10
• 125000006279 3-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Br)=C1[H])C([H])([H])* 0.000 claims description 10
• 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 claims description 10
• 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 claims description 10
• 125000006482 3-iodobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(I)=C1[H])C([H])([H])* 0.000 claims description 10
• 125000006497 3-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims description 10
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 10
• 125000006495 3-trifluoromethyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1[H])C([H])([H])*)C(F)(F)F 0.000 claims description 10
• 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims description 10
• WNWVKZTYMQWFHE-UHFFFAOYSA-N 4-ethylmorpholine Chemical group [CH2]CN1CCOCC1 WNWVKZTYMQWFHE-UHFFFAOYSA-N 0.000 claims description 10
• 125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 claims description 10
• 125000000173 4-trifluoromethoxy benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC(F)(F)F)C([H])([H])* 0.000 claims description 10
• 208000020576 Adrenal disease Diseases 0.000 claims description 10
• 208000000094 Chronic Pain Diseases 0.000 claims description 10
• 206010011224 Cough Diseases 0.000 claims description 10
• 208000011231 Crohn disease Diseases 0.000 claims description 10
• 208000030814 Eating disease Diseases 0.000 claims description 10
• 208000019454 Feeding and Eating disease Diseases 0.000 claims description 10
• 206010020772 Hypertension Diseases 0.000 claims description 10
• DGYIJVNZSDYBOE-UHFFFAOYSA-N [CH2]C1=CC=NC=C1 Chemical group [CH2]C1=CC=NC=C1 DGYIJVNZSDYBOE-UHFFFAOYSA-N 0.000 claims description 10
• 208000005298 acute pain Diseases 0.000 claims description 10
• 206010003119 arrhythmia Diseases 0.000 claims description 10
• 208000006673 asthma Diseases 0.000 claims description 10
• 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 10
• 125000004744 butyloxycarbonyl group Chemical group 0.000 claims description 10
• 230000019771 cognition Effects 0.000 claims description 10
• 235000014632 disordered eating Nutrition 0.000 claims description 10
• 239000003937 drug carrier Substances 0.000 claims description 10
• 208000004296 neuralgia Diseases 0.000 claims description 10
• 208000021722 neuropathic pain Diseases 0.000 claims description 10
• 201000009032 substance abuse Diseases 0.000 claims description 10
• 231100000736 substance abuse Toxicity 0.000 claims description 10
• 208000011117 substance-related disease Diseases 0.000 claims description 10
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 9
• 125000005806 3,4,5-trimethoxybenzyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1C([H])([H])* 0.000 claims description 9
• 125000006512 3,4-dichlorobenzyl group Chemical group [H]C1=C(Cl)C(Cl)=C([H])C(=C1[H])C([H])([H])* 0.000 claims description 9
• 125000002774 3,4-dimethoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims description 9
• 125000001318 4-trifluoromethylbenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])*)C(F)(F)F 0.000 claims description 9
• 208000024827 Alzheimer disease Diseases 0.000 claims description 9
• 206010012289 Dementia Diseases 0.000 claims description 9
• 206010026749 Mania Diseases 0.000 claims description 9
• 208000008589 Obesity Diseases 0.000 claims description 9
• 208000028017 Psychotic disease Diseases 0.000 claims description 9
• 206010046543 Urinary incontinence Diseases 0.000 claims description 9
• 235000019788 craving Nutrition 0.000 claims description 9
• 206010012601 diabetes mellitus Diseases 0.000 claims description 9
• 206010015037 epilepsy Diseases 0.000 claims description 9
• 208000002551 irritable bowel syndrome Diseases 0.000 claims description 9
• 230000036651 mood Effects 0.000 claims description 9
• 235000020824 obesity Nutrition 0.000 claims description 9
• 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 claims description 9
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 9
• 201000000980 schizophrenia Diseases 0.000 claims description 9
• 230000006641 stabilisation Effects 0.000 claims description 9
• 238000011105 stabilization Methods 0.000 claims description 9
• 208000020925 Bipolar disease Diseases 0.000 claims description 8
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 8
• 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 7
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
• 125000005322 morpholin-1-yl group Chemical group 0.000 claims description 7
• 125000000286 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 7
• ZYHQGITXIJDDKC-UHFFFAOYSA-N 2-[2-(2-aminophenyl)ethyl]aniline Chemical group NC1=CC=CC=C1CCC1=CC=CC=C1N ZYHQGITXIJDDKC-UHFFFAOYSA-N 0.000 claims description 6
• 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 6
• UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 claims description 6
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
• 125000004432 carbon atom Chemical group C* 0.000 claims description 6
• 125000003386 piperidinyl group Chemical group 0.000 claims description 6
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
• 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 claims description 6
• 125000001847 2-phenylcyclopropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1([H])C([H])([H])C1([H])* 0.000 claims description 5
• 125000004062 acenaphthenyl group Chemical group C1(CC2=CC=CC3=CC=CC1=C23)* 0.000 claims description 5
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 5
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
• 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 5
• 238000002156 mixing Methods 0.000 claims description 5
• 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 4
• 125000004414 alkyl thio group Chemical group 0.000 claims description 4
• 125000000304 alkynyl group Chemical group 0.000 claims description 4
• 125000004104 aryloxy group Chemical group 0.000 claims description 4
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 4
• 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 4
• 125000005885 heterocycloalkylalkyl group Chemical group 0.000 claims description 4
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
• 125000002883 imidazolyl group Chemical group 0.000 claims description 4
• 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 4
• ALXBWOVLKSYZNY-RUZDIDTESA-N 3-[(2r)-3-amino-2-hydroxypropyl]-1-(4-fluorophenyl)-8-[(8-methylnaphthalen-1-yl)methyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C=12C(C)=CC=CC2=CC=CC=1CN(CC1)CCC1(C(N(C[C@H](O)CN)C1)=O)N1C1=CC=C(F)C=C1 ALXBWOVLKSYZNY-RUZDIDTESA-N 0.000 claims description 3
• 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 3
• 125000006630 butoxycarbonylamino group Chemical group 0.000 claims description 3
• 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 3
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• 201000010099 disease Diseases 0.000 claims description 3
• 125000002541 furyl group Chemical group 0.000 claims description 3
• 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 claims description 3
• 125000004605 1,2,3,4-tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 claims description 2
• OYGRPMXMTBVAQE-MUUNZHRXSA-N 1-(4-fluorophenyl)-3-[(2r)-2-hydroxy-3-(3-hydroxypropylamino)propyl]-8-[(8-methylnaphthalen-1-yl)methyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C=12C(C)=CC=CC2=CC=CC=1CN(CC1)CCC1(C(N(C[C@H](O)CNCCCO)C1)=O)N1C1=CC=C(F)C=C1 OYGRPMXMTBVAQE-MUUNZHRXSA-N 0.000 claims description 2
• IMGQPABKFUXCTN-GDLZYMKVSA-N 1-(4-fluorophenyl)-3-[(2r)-2-hydroxy-3-[3-(methylamino)propylamino]propyl]-8-[(8-methylnaphthalen-1-yl)methyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C1CN(CC=2C3=C(C)C=CC=C3C=CC=2)CCC21C(=O)N(C[C@H](O)CNCCCNC)CN2C1=CC=C(F)C=C1 IMGQPABKFUXCTN-GDLZYMKVSA-N 0.000 claims description 2
• AWYSBTQCCOWYQC-HHHXNRCGSA-N 3-[(2r)-3-(dimethylamino)-2-hydroxypropyl]-1-(4-fluorophenyl)-8-[(8-methylnaphthalen-1-yl)methyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C1CN(CC=2C3=C(C)C=CC=C3C=CC=2)CCC21C(=O)N(C[C@H](O)CN(C)C)CN2C1=CC=C(F)C=C1 AWYSBTQCCOWYQC-HHHXNRCGSA-N 0.000 claims description 2
• HWQFSZPVJZOLNP-SSEXGKCCSA-N 3-[(2r)-3-[3-(dimethylamino)propylamino]-2-hydroxypropyl]-1-(4-fluorophenyl)-8-[(8-methylnaphthalen-1-yl)methyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C1CN(CC=2C3=C(C)C=CC=C3C=CC=2)CCC21C(=O)N(C[C@H](O)CNCCCN(C)C)CN2C1=CC=C(F)C=C1 HWQFSZPVJZOLNP-SSEXGKCCSA-N 0.000 claims description 2
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