NZ543451A - Substituted 3-alkyl and 3-alkenyl azetidine derivitives - Google Patents

Info

Publication number

NZ543451A

NZ543451A NZ543451A NZ54345104A NZ543451A NZ 543451 A NZ543451 A NZ 543451A NZ 543451 A NZ543451 A NZ 543451A NZ 54345104 A NZ54345104 A NZ 54345104A NZ 543451 A NZ543451 A NZ 543451A

Authority

NZ

New Zealand

Prior art keywords

methyl

azetidin

chlorophenyl

difluorophenyl

fluoro

Prior art date

2003-06-11

Links

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• 150000001875 compounds Chemical class 0.000 claims abstract description 260
• 125000001424 substituent group Chemical group 0.000 claims abstract description 154
• 238000011282 treatment Methods 0.000 claims abstract description 78
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 38
• 230000002265 prevention Effects 0.000 claims abstract description 27
• 208000035475 disorder Diseases 0.000 claims abstract description 22
• 201000010099 disease Diseases 0.000 claims abstract description 16
• 235000014632 disordered eating Nutrition 0.000 claims abstract description 12
• 206010010774 Constipation Diseases 0.000 claims abstract description 11
• 208000019425 cirrhosis of liver Diseases 0.000 claims abstract description 11
• 208000030814 Eating disease Diseases 0.000 claims abstract description 10
• 208000019454 Feeding and Eating disease Diseases 0.000 claims abstract description 10
• 206010016654 Fibrosis Diseases 0.000 claims abstract description 10
• 230000001404 mediated effect Effects 0.000 claims abstract description 10
• 208000011117 substance-related disease Diseases 0.000 claims abstract description 9
• 201000009032 substance abuse Diseases 0.000 claims abstract description 8
• 208000006673 asthma Diseases 0.000 claims abstract description 7
• 208000014797 chronic intestinal pseudoobstruction Diseases 0.000 claims abstract description 7
• 230000007882 cirrhosis Effects 0.000 claims abstract description 7
• 210000004185 liver Anatomy 0.000 claims abstract description 7
• 231100000736 substance abuse Toxicity 0.000 claims abstract description 7
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 279
• -1 (2) pyridyl Chemical group 0.000 claims description 260
• JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 232
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 114
• 125000000217 alkyl group Chemical group 0.000 claims description 96
• 125000004567 azetidin-3-yl group Chemical group N1CC(C1)* 0.000 claims description 86
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 86
• 239000000203 mixture Substances 0.000 claims description 81
• 150000002367 halogens Chemical class 0.000 claims description 78
• 229910052736 halogen Inorganic materials 0.000 claims description 76
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 72
• 125000003118 aryl group Chemical group 0.000 claims description 71
• 239000001257 hydrogen Substances 0.000 claims description 70
• 229910052739 hydrogen Inorganic materials 0.000 claims description 70
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 64
• 150000003839 salts Chemical class 0.000 claims description 61
• 125000001072 heteroaryl group Chemical group 0.000 claims description 54
• 208000008589 Obesity Diseases 0.000 claims description 49
• 235000020824 obesity Nutrition 0.000 claims description 49
• 229910052799 carbon Inorganic materials 0.000 claims description 45
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 44
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 38
• 150000002431 hydrogen Chemical class 0.000 claims description 32
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 29
• 125000003342 alkenyl group Chemical group 0.000 claims description 28
• 150000001721 carbon Chemical group 0.000 claims description 27
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 26
• 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims description 25
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 24
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 24
• 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 23
• 239000003814 drug Substances 0.000 claims description 23
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 22
• 125000000304 alkynyl group Chemical group 0.000 claims description 22
• HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims description 22
• 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 21
• 150000001412 amines Chemical class 0.000 claims description 21
• 125000001153 fluoro group Chemical group F* 0.000 claims description 21
• ILFIRBGRMCGNOO-UHFFFAOYSA-N 1,1-bis($l^{1}-oxidanyl)ethene Chemical group [O]C([O])=C ILFIRBGRMCGNOO-UHFFFAOYSA-N 0.000 claims description 20
• 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 20
• QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 20
• 229910052757 nitrogen Inorganic materials 0.000 claims description 20
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 18
• 125000004076 pyridyl group Chemical group 0.000 claims description 18
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 15
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 14
• 125000004429 atom Chemical group 0.000 claims description 14
• 125000001544 thienyl group Chemical group 0.000 claims description 14
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 13
• 239000003937 drug carrier Substances 0.000 claims description 13
• 125000000623 heterocyclic group Chemical group 0.000 claims description 12
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 11
• 125000005842 heteroatom Chemical group 0.000 claims description 10
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 10
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
• 229910052760 oxygen Inorganic materials 0.000 claims description 10
• 229910052717 sulfur Inorganic materials 0.000 claims description 10
• PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 9
• 230000037406 food intake Effects 0.000 claims description 9
• 235000012631 food intake Nutrition 0.000 claims description 9
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
• 125000004104 aryloxy group Chemical group 0.000 claims description 8
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 8
• 239000001301 oxygen Substances 0.000 claims description 8
• 239000011593 sulfur Chemical group 0.000 claims description 8
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 7
• 125000004432 carbon atom Chemical group C* 0.000 claims description 7
• 229910052702 rhenium Inorganic materials 0.000 claims description 7
• 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims description 6
• 208000028017 Psychotic disease Diseases 0.000 claims description 6
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
• 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 6
• 238000009472 formulation Methods 0.000 claims description 6
• 125000005843 halogen group Chemical group 0.000 claims description 6
• 238000004519 manufacturing process Methods 0.000 claims description 6
• 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 6
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 6
• 201000000980 schizophrenia Diseases 0.000 claims description 6
• LOVPHSMOAVXQIH-UHFFFAOYSA-N (4-nitrophenyl) hydrogen carbonate Chemical compound OC(=O)OC1=CC=C([N+]([O-])=O)C=C1 LOVPHSMOAVXQIH-UHFFFAOYSA-N 0.000 claims description 5
• 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims description 5
• 208000019901 Anxiety disease Diseases 0.000 claims description 5
• 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 5
• 241000124008 Mammalia Species 0.000 claims description 5
• DWLVWMUCHSLGSU-UHFFFAOYSA-M n,n-dimethylcarbamate Chemical compound CN(C)C([O-])=O DWLVWMUCHSLGSU-UHFFFAOYSA-M 0.000 claims description 5
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
• 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 claims description 4
• 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 4
• 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 4
• 208000019695 Migraine disease Diseases 0.000 claims description 4
• 241000699670 Mus sp. Species 0.000 claims description 4
• 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 claims description 4
• 125000003545 alkoxy group Chemical group 0.000 claims description 4
• 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 4
• 125000005129 aryl carbonyl group Chemical group 0.000 claims description 4
• 125000005199 aryl carbonyloxy group Chemical group 0.000 claims description 4
• 239000000460 chlorine Substances 0.000 claims description 4
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
• 206010027599 migraine Diseases 0.000 claims description 4
• 230000004044 response Effects 0.000 claims description 4
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• 125000001960 7 membered carbocyclic group Chemical group 0.000 claims description 3
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• DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 3
• 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 3
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• GZPHSAQLYPIAIN-UHFFFAOYSA-N 3-pyridinecarbonitrile Chemical compound N#CC1=CC=CN=C1 GZPHSAQLYPIAIN-UHFFFAOYSA-N 0.000 claims description 2
• 208000010235 Food Addiction Diseases 0.000 claims description 2
• GMFGENLXAWETEK-UHFFFAOYSA-N [1-[1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene]-1-(3,5-difluorophenyl)propan-2-yl] n-propan-2-ylcarbamate Chemical compound C=1C(F)=CC(F)=CC=1C(C(C)OC(=O)NC(C)C)=C(C1)CN1C(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 GMFGENLXAWETEK-UHFFFAOYSA-N 0.000 claims description 2
• OFJLSOXXIMLDDL-UHFFFAOYSA-N ethyl (4-nitrophenyl) carbonate Chemical compound CCOC(=O)OC1=CC=C([N+]([O-])=O)C=C1 OFJLSOXXIMLDDL-UHFFFAOYSA-N 0.000 claims description 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
• CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 2
• ATIDGLSLFKOOCE-UHFFFAOYSA-N 1-[1-[bis(4-chlorophenyl)methyl]azetidin-3-yl]-1-(3,5-difluorophenyl)propan-2-ol Chemical compound C=1C(F)=CC(F)=CC=1C(C(O)C)C(C1)CN1C(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 ATIDGLSLFKOOCE-UHFFFAOYSA-N 0.000 claims 3
• JGRPZAGOYKNIAC-UHFFFAOYSA-N ethyl n-propan-2-ylcarbamate Chemical compound CCOC(=O)NC(C)C JGRPZAGOYKNIAC-UHFFFAOYSA-N 0.000 claims 2
• GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims 2
• YYESFPVLOJOMPC-UHFFFAOYSA-N 1-(3,5-difluorophenyl)-2-methylpropan-2-ol Chemical compound CC(C)(O)CC1=CC(F)=CC(F)=C1 YYESFPVLOJOMPC-UHFFFAOYSA-N 0.000 claims 1
• QLHXUURSZHULTA-UHFFFAOYSA-N 1-[1-[bis(4-chlorophenyl)methyl]azetidin-3-yl]-1-(3,5-difluorophenyl)propan-2-one Chemical compound C=1C(F)=CC(F)=CC=1C(C(=O)C)C(C1)CN1C(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 QLHXUURSZHULTA-UHFFFAOYSA-N 0.000 claims 1
• HJVCJGUTCZTKBU-UHFFFAOYSA-N 3-[1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene]-3-(3,5-difluorophenyl)-2,2-dimethylpropanenitrile Chemical compound C=1C(F)=CC(F)=CC=1C(C(C)(C#N)C)=C(C1)CN1C(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 HJVCJGUTCZTKBU-UHFFFAOYSA-N 0.000 claims 1
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