JP2005500321A5 - - Google Patents

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Publication number

JP2005500321A5

JP2005500321A5 JP2003508934A JP2003508934A JP2005500321A5 JP 2005500321 A5 JP2005500321 A5 JP 2005500321A5 JP 2003508934 A JP2003508934 A JP 2003508934A JP 2003508934 A JP2003508934 A JP 2003508934A JP 2005500321 A5 JP2005500321 A5 JP 2005500321A5

Authority

JP

Japan

Prior art keywords

amino

acetyl

compound

compound according

fluoro

Prior art date

2002-06-26

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.)

Granted

Links

• Espacenet
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• 150000001875 compounds Chemical class 0.000 claims 41
• -1 isopropylsulfonyl Chemical group 0.000 claims 13
• 201000010099 disease Diseases 0.000 claims 10
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 10
• 125000003118 aryl group Chemical group 0.000 claims 8
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 7
• 125000000217 alkyl group Chemical group 0.000 claims 5
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims 5
• 239000003814 drug Substances 0.000 claims 4
• 229910052736 halogen Inorganic materials 0.000 claims 4
• 238000004519 manufacturing process Methods 0.000 claims 4
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
• 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
• 108090000194 Dipeptidyl-peptidases and tripeptidyl-peptidases Proteins 0.000 claims 3
• 102000003779 Dipeptidyl-peptidases and tripeptidyl-peptidases Human genes 0.000 claims 3
• 108010022999 Serine Proteases Proteins 0.000 claims 3
• 102000012479 Serine Proteases Human genes 0.000 claims 3
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 3
• 125000004093 cyano group Chemical group *C#N 0.000 claims 3
• 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims 3
• 125000003107 substituted aryl group Chemical group 0.000 claims 3
• 208000023275 Autoimmune disease Diseases 0.000 claims 2
• 206010007559 Cardiac failure congestive Diseases 0.000 claims 2
• 206010010774 Constipation Diseases 0.000 claims 2
• 208000018522 Gastrointestinal disease Diseases 0.000 claims 2
• 206010018364 Glomerulonephritis Diseases 0.000 claims 2
• 208000031886 HIV Infections Diseases 0.000 claims 2
• 208000037357 HIV infectious disease Diseases 0.000 claims 2
• 206010019280 Heart failures Diseases 0.000 claims 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
• 208000031226 Hyperlipidaemia Diseases 0.000 claims 2
• 206010020751 Hypersensitivity Diseases 0.000 claims 2
• 206010020772 Hypertension Diseases 0.000 claims 2
• 206010061218 Inflammation Diseases 0.000 claims 2
• QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 2
• 206010049287 Lipodystrophy acquired Diseases 0.000 claims 2
• 208000008589 Obesity Diseases 0.000 claims 2
• 108091005804 Peptidases Proteins 0.000 claims 2
• 102000035195 Peptidases Human genes 0.000 claims 2
• 239000004365 Protease Substances 0.000 claims 2
• 201000004681 Psoriasis Diseases 0.000 claims 2
• 206010052779 Transplant rejections Diseases 0.000 claims 2
• 235000004279 alanine Nutrition 0.000 claims 2
• 208000026935 allergic disease Diseases 0.000 claims 2
• 230000007815 allergy Effects 0.000 claims 2
• 206010003246 arthritis Diseases 0.000 claims 2
• 238000003776 cleavage reaction Methods 0.000 claims 2
• 230000000295 complement effect Effects 0.000 claims 2
• 230000003001 depressive effect Effects 0.000 claims 2
• 206010012601 diabetes mellitus Diseases 0.000 claims 2
• 208000010643 digestive system disease Diseases 0.000 claims 2
• 208000016097 disease of metabolism Diseases 0.000 claims 2
• 201000002491 encephalomyelitis Diseases 0.000 claims 2
• 208000018685 gastrointestinal system disease Diseases 0.000 claims 2
• 125000001188 haloalkyl group Chemical group 0.000 claims 2
• 125000005843 halogen group Chemical group 0.000 claims 2
• 150000002367 halogens Chemical class 0.000 claims 2
• 208000024348 heart neoplasm Diseases 0.000 claims 2
• 125000001072 heteroaryl group Chemical group 0.000 claims 2
• 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 claims 2
• 230000006698 induction Effects 0.000 claims 2
• 208000027866 inflammatory disease Diseases 0.000 claims 2
• 230000004054 inflammatory process Effects 0.000 claims 2
• 230000005764 inhibitory process Effects 0.000 claims 2
• 208000006132 lipodystrophy Diseases 0.000 claims 2
• 230000001404 mediated effect Effects 0.000 claims 2
• 208000030159 metabolic disease Diseases 0.000 claims 2
• 235000020824 obesity Nutrition 0.000 claims 2
• 230000002265 prevention Effects 0.000 claims 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
• 235000019419 proteases Nutrition 0.000 claims 2
• 230000007017 scission Effects 0.000 claims 2
• 230000001568 sexual effect Effects 0.000 claims 2
• 230000000451 tissue damage Effects 0.000 claims 2
• 231100000827 tissue damage Toxicity 0.000 claims 2
• 230000003612 virological effect Effects 0.000 claims 2
• OPUFELCSQJILAQ-ZDUSSCGKSA-N (2s)-4,4-difluoro-1-[2-[(1-propan-2-ylsulfonylpiperidin-4-yl)amino]acetyl]pyrrolidine-2-carbonitrile Chemical compound C1CN(S(=O)(=O)C(C)C)CCC1NCC(=O)N1[C@H](C#N)CC(F)(F)C1 OPUFELCSQJILAQ-ZDUSSCGKSA-N 0.000 claims 1
• WRTLMQCEYAWWPP-AKXYIILFSA-N (2s,4s)-1-[2-[(1-benzylpiperidin-4-yl)amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(CC=2C=CC=CC=2)CC1 WRTLMQCEYAWWPP-AKXYIILFSA-N 0.000 claims 1
• LVHXEXIIDKEIPP-AKXYIILFSA-N (2s,4s)-1-[2-[(1-benzylsulfonylpiperidin-4-yl)amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(S(=O)(=O)CC=2C=CC=CC=2)CC1 LVHXEXIIDKEIPP-AKXYIILFSA-N 0.000 claims 1
• UBZFTZRGRHQOJX-BOQFCEBISA-N (2s,4s)-1-[2-[(4-tert-butylcyclohexyl)amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1CC(C(C)(C)C)CCC1NCC(=O)N1[C@H](C#N)C[C@H](F)C1 UBZFTZRGRHQOJX-BOQFCEBISA-N 0.000 claims 1
• OVUYRWRLWZZUPX-SLHAJLBXSA-N (2s,4s)-1-[2-[[1-(1,3-benzoxazol-2-yl)piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2OC3=CC=CC=C3N=2)CC1 OVUYRWRLWZZUPX-SLHAJLBXSA-N 0.000 claims 1
• WACWKVFHKYZGHQ-RVXRQPKJSA-N (2s,4s)-1-[2-[[1-(3,5-difluorophenyl)piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=C(F)C=C(F)C=2)CC1 WACWKVFHKYZGHQ-RVXRQPKJSA-N 0.000 claims 1
• DTUFGVZMAPUSSA-NKGQWRHHSA-N (2s,4s)-1-[2-[[1-(3-cyano-5-fluorophenyl)piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=C(C=C(F)C=2)C#N)CC1 DTUFGVZMAPUSSA-NKGQWRHHSA-N 0.000 claims 1
• ANKZSGQYBFVBBZ-NXCSSKFKSA-N (2s,4s)-1-[2-[[1-(4-cyano-3,5-difluorophenyl)piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=C(F)C(C#N)=C(F)C=2)CC1 ANKZSGQYBFVBBZ-NXCSSKFKSA-N 0.000 claims 1
• DRUIBBVCAZXTTP-RVXRQPKJSA-N (2s,4s)-1-[2-[[1-(4-cyano-3-fluorophenyl)piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=C(F)C(C#N)=CC=2)CC1 DRUIBBVCAZXTTP-RVXRQPKJSA-N 0.000 claims 1
• NSYIJUBKYPUKAX-NKGQWRHHSA-N (2s,4s)-1-[2-[[1-(4-cyanophenyl)piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=CC(=CC=2)C#N)CC1 NSYIJUBKYPUKAX-NKGQWRHHSA-N 0.000 claims 1
• ACSUPYXNJOORJZ-JCTRNDEQSA-N (2s,4s)-1-[2-[[1-[[(1r,4r)-7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl]methylsulfonyl]piperidin-4-yl]amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C([C@]12CC[C@](CC2=O)(C1(C)C)[H])S(=O)(=O)N(CC1)CCC1NCC(=O)N1C[C@@H](F)C[C@H]1C#N ACSUPYXNJOORJZ-JCTRNDEQSA-N 0.000 claims 1
• VHUBGESORNJERA-JGAZGGJJSA-N (2s,4s)-4-fluoro-1-[2-[(1-propan-2-ylsulfonylazetidin-3-yl)amino]acetyl]pyrrolidine-2-carbonitrile;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.C1N(S(=O)(=O)C(C)C)CC1NCC(=O)N1[C@H](C#N)C[C@H](F)C1 VHUBGESORNJERA-JGAZGGJJSA-N 0.000 claims 1
• DWBYBRXMQPLWDY-KYSPHBLOSA-N (2s,4s)-4-fluoro-1-[2-[(1-propan-2-ylsulfonylpiperidin-4-yl)amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1CN(S(=O)(=O)C(C)C)CCC1NCC(=O)N1[C@H](C#N)C[C@H](F)C1 DWBYBRXMQPLWDY-KYSPHBLOSA-N 0.000 claims 1
• NNERJDDFTOBJMK-GFCHTBATSA-N (2s,4s)-4-fluoro-1-[2-[(4-phenylcyclohexyl)amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCC(C=2C=CC=CC=2)CC1 NNERJDDFTOBJMK-GFCHTBATSA-N 0.000 claims 1
• YQOFAJUZCPUBIY-NOUACQEWSA-N (2s,4s)-4-fluoro-1-[2-[(4-pyridin-2-ylcyclohexyl)amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCC(C=2N=CC=CC=2)CC1 YQOFAJUZCPUBIY-NOUACQEWSA-N 0.000 claims 1
• JNXGTJWRFVXMPP-XJPBFQKESA-N (2s,4s)-4-fluoro-1-[2-[[(3s)-1-(4-fluorophenyl)-2-oxopyrrolidin-3-yl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CN[C@@H]1C(=O)N(C=2C=CC(F)=CC=2)CC1 JNXGTJWRFVXMPP-XJPBFQKESA-N 0.000 claims 1
• BERDFKIYBWEOSD-NLQWVURJSA-N (2s,4s)-4-fluoro-1-[2-[[(3s)-1-[(4-fluorophenyl)methyl]-2-oxopyrrolidin-3-yl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CN[C@@H]1C(=O)N(CC=2C=CC(F)=CC=2)CC1 BERDFKIYBWEOSD-NLQWVURJSA-N 0.000 claims 1
• LUSSRHVVCAVZLE-QQTWVUFVSA-N (2s,4s)-4-fluoro-1-[2-[[1-(2,4,6-trimethylphenyl)sulfonylpiperidin-4-yl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.CC1=CC(C)=CC(C)=C1S(=O)(=O)N1CCC(NCC(=O)N2[C@@H](C[C@H](F)C2)C#N)CC1 LUSSRHVVCAVZLE-QQTWVUFVSA-N 0.000 claims 1
• RHCGCNFKRGPVNR-DTRWSJPISA-N (2s,4s)-4-fluoro-1-[2-[[1-(2-naphthalen-1-ylethylsulfonyl)piperidin-4-yl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(S(=O)(=O)CCC=2C3=CC=CC=C3C=CC=2)CC1 RHCGCNFKRGPVNR-DTRWSJPISA-N 0.000 claims 1
• FGPQHACKOPAXDB-RVXRQPKJSA-N (2s,4s)-4-fluoro-1-[2-[[1-(4-fluorophenyl)piperidin-4-yl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=CC(F)=CC=2)CC1 FGPQHACKOPAXDB-RVXRQPKJSA-N 0.000 claims 1
• VIHJGAXRUVXCPZ-GUYCJALGSA-N (2s,4s)-4-fluoro-1-[2-[[1-(4-nitrophenyl)piperidin-4-yl]amino]acetyl]pyrrolidine-2-carbonitrile Chemical compound C1=CC([N+](=O)[O-])=CC=C1N1CCC(NCC(=O)N2[C@@H](C[C@H](F)C2)C#N)CC1 VIHJGAXRUVXCPZ-GUYCJALGSA-N 0.000 claims 1
• DYYGVUFTZUQBLH-RVXRQPKJSA-N (2s,4s)-4-fluoro-1-[2-[[1-[4-(trifluoromethyl)phenyl]piperidin-4-yl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCN(C=2C=CC(=CC=2)C(F)(F)F)CC1 DYYGVUFTZUQBLH-RVXRQPKJSA-N 0.000 claims 1
• QTPPIDJMVPSOED-SLRFVWSASA-N (2s,4s)-4-fluoro-1-[2-[[4-(4-fluorophenyl)cyclohexyl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCC(C=2C=CC(F)=CC=2)CC1 QTPPIDJMVPSOED-SLRFVWSASA-N 0.000 claims 1
• PBKLJUYHVKLTJU-SLRFVWSASA-N (2s,4s)-4-fluoro-1-[2-[[4-[4-(trifluoromethyl)phenyl]cyclohexyl]amino]acetyl]pyrrolidine-2-carbonitrile;hydrochloride Chemical compound Cl.C1[C@@H](F)C[C@@H](C#N)N1C(=O)CNC1CCC(C=2C=CC(=CC=2)C(F)(F)F)CC1 PBKLJUYHVKLTJU-SLRFVWSASA-N 0.000 claims 1
• 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
• AFWRAOQZVKXIAJ-KKUMJFAQSA-N 6-[(3s)-3-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]pyrrolidin-1-yl]pyridine-3-carbonitrile Chemical compound C1[C@@H](F)C[C@@H](C#N)N1C(=O)CN[C@@H]1CN(C=2N=CC(=CC=2)C#N)CC1 AFWRAOQZVKXIAJ-KKUMJFAQSA-N 0.000 claims 1
• 206010011703 Cyanosis Diseases 0.000 claims 1
• 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 claims 1
• 102100020751 Dipeptidyl peptidase 2 Human genes 0.000 claims 1
• 101710087084 Dipeptidyl peptidase 2 Proteins 0.000 claims 1
• 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 claims 1
• DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims 1
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
• 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
• 239000003937 drug carrier Substances 0.000 claims 1
• 230000004064 dysfunction Effects 0.000 claims 1
• PZNDZJXROVAHOH-VRDPANCYSA-N ethyl 3-[[2-[(2s,4s)-2-cyano-4-fluoropyrrolidin-1-yl]-2-oxoethyl]amino]-8-azabicyclo[3.2.1]octane-8-carboxylate;hydrochloride Chemical compound Cl.CCOC(=O)N1C(C2)CCC1CC2NCC(=O)N1C[C@@H](F)C[C@H]1C#N PZNDZJXROVAHOH-VRDPANCYSA-N 0.000 claims 1
• 206010016165 failure to thrive Diseases 0.000 claims 1
• 150000002825 nitriles Chemical class 0.000 claims 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
• 239000008194 pharmaceutical composition Substances 0.000 claims 1
• 239000000825 pharmaceutical preparation Substances 0.000 claims 1
• 125000004076 pyridyl group Chemical group 0.000 claims 1
• 239000000126 substance Substances 0.000 claims 1
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
• 230000001225 therapeutic effect Effects 0.000 claims 1