JP2006512311A5 - - Google Patents
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- JP2006512311A5 JP2006512311A5 JP2004548847A JP2004548847A JP2006512311A5 JP 2006512311 A5 JP2006512311 A5 JP 2006512311A5 JP 2004548847 A JP2004548847 A JP 2004548847A JP 2004548847 A JP2004548847 A JP 2004548847A JP 2006512311 A5 JP2006512311 A5 JP 2006512311A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- benzo
- amino
- methyl
- 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.)
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- -1 1,4-dihydro-quinazolinyl Chemical group 0.000 claims 247
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 21
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 18
- 125000005605 benzo group Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 16
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 13
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 claims 12
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 12
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 11
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 11
- 239000000460 chlorine Substances 0.000 claims 11
- 229910052801 chlorine Inorganic materials 0.000 claims 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims 11
- 229910052731 fluorine Inorganic materials 0.000 claims 11
- 239000011737 fluorine Substances 0.000 claims 11
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- 150000003839 salts Chemical class 0.000 claims 9
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 7
- 125000003282 alkyl amino group Chemical group 0.000 claims 7
- 229910052794 bromium Inorganic materials 0.000 claims 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 7
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 7
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 6
- 125000000623 heterocyclic group Chemical group 0.000 claims 6
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 6
- 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 6
- 125000006239 protecting group Chemical group 0.000 claims 6
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 5
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 5
- 125000003277 amino group Chemical group 0.000 claims 5
- 125000002785 azepinyl group Chemical group 0.000 claims 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 5
- UZVGSSNIUNSOFA-UHFFFAOYSA-N dibenzofuran-1-carboxylic acid Chemical compound O1C2=CC=CC=C2C2=C1C=CC=C2C(=O)O UZVGSSNIUNSOFA-UHFFFAOYSA-N 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- 125000004434 sulfur atom Chemical group 0.000 claims 5
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims 5
- 125000006563 (C1-3) alkylaminocarbonyl group Chemical group 0.000 claims 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 125000006576 di-(C1-C3-alkyl)-aminocarbonyl group Chemical group 0.000 claims 4
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 229910052740 iodine Inorganic materials 0.000 claims 4
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 4
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 3
- 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 150000001721 carbon Chemical group 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- 125000006597 (C1-C3) alkylcarbonylamino group Chemical group 0.000 claims 2
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 claims 2
- 125000006602 (C1-C3) alkylsulfonylamino group Chemical group 0.000 claims 2
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- ZFJAEKNTWCKVJQ-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-1-(2,1,3-benzoxadiazol-5-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC3=CC4=NON=C4C=C3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 ZFJAEKNTWCKVJQ-UHFFFAOYSA-N 0.000 claims 2
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical group O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 2
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 2
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 239000000969 carrier Substances 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims 2
- 125000001041 indolyl group Chemical group 0.000 claims 2
- 150000007529 inorganic bases Chemical class 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 2
- 150000007522 mineralic acids Chemical class 0.000 claims 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 2
- 150000007524 organic acids Chemical class 0.000 claims 2
- 150000007530 organic bases Chemical class 0.000 claims 2
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 2
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 claims 2
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- 125000006599 (C1-C3) alkylaminocarbonylamino group Chemical group 0.000 claims 1
- 125000006603 (C1-C3) alkylaminosulfonyl group Chemical group 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 1
- LVDPOWHAVPDMHP-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-1-(11h-benzo[c][1]benzazepin-6-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4CC4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 LVDPOWHAVPDMHP-UHFFFAOYSA-N 0.000 claims 1
- XWEOHAJQVMIKGZ-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-1-(benzo[b][1,4]benzoxazepin-6-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4OC4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 XWEOHAJQVMIKGZ-UHFFFAOYSA-N 0.000 claims 1
- YDWBSAMIOHUVDL-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-1-(benzo[c][1,8]naphthyridin-6-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4C4=CC=CN=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 YDWBSAMIOHUVDL-UHFFFAOYSA-N 0.000 claims 1
- OQCYQTBTYPXVRI-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-1-(benzo[h][1,6]naphthyridin-5-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CN=C4C4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 OQCYQTBTYPXVRI-UHFFFAOYSA-N 0.000 claims 1
- JIZNYPIAZNKEPY-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-3-methyl-7-(3-methylbut-2-enyl)-1-[(1-methyl-2,2-dioxo-2$l^{6},1-benzothiazin-4-yl)methyl]purine-2,6-dione Chemical compound C=1S(=O)(=O)N(C)C2=CC=CC=C2C=1CN(C(C=1N2CC=C(C)C)=O)C(=O)N(C)C=1N=C2N1CCCC(N)C1 JIZNYPIAZNKEPY-UHFFFAOYSA-N 0.000 claims 1
- XYYQUFIYMPYZQO-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-3-methyl-7-(3-methylbut-2-enyl)-1-[(3-oxoisoindol-1-ylidene)methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(C=C3C4=CC=CC=C4C(=O)N3)C(=O)C=2N(CC=C(C)C)C=1N1CCCC(N)C1 XYYQUFIYMPYZQO-UHFFFAOYSA-N 0.000 claims 1
- XSEAMCPQTZGEOJ-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-1-(1,4-dihydroquinazolin-2-ylmethyl)-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3NCC4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 XSEAMCPQTZGEOJ-UHFFFAOYSA-N 0.000 claims 1
- HDUURJUYHXNGNB-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-1-(2,3-dihydro-1,4-benzoxazepin-5-ylmethyl)-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4OCCN=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 HDUURJUYHXNGNB-UHFFFAOYSA-N 0.000 claims 1
- UJCXAPHOXHYFDJ-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-1-(imidazo[2,1-a]isoquinolin-2-ylmethyl)-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3N=C4C5=CC=CC=C5C=CN4C=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 UJCXAPHOXHYFDJ-UHFFFAOYSA-N 0.000 claims 1
- IIFWKNLPZOLJAK-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-cyclopropyl-1-(phenanthridin-6-ylmethyl)purine-2,6-dione Chemical compound O=C1N(CC=2C3=CC=CC=C3C3=CC=CC=C3N=2)C(=O)C=2N(CC#CC)C(N3CC(N)CCC3)=NC=2N1C1CC1 IIFWKNLPZOLJAK-UHFFFAOYSA-N 0.000 claims 1
- FOFYBZQYNQXNIE-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(1,2,3,4-tetrahydrophenanthridin-6-ylmethyl)purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4C=4CCCCC=4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 FOFYBZQYNQXNIE-UHFFFAOYSA-N 0.000 claims 1
- KOYKKFVARVTVBE-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(phenanthridin-6-ylmethyl)purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4C4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 KOYKKFVARVTVBE-UHFFFAOYSA-N 0.000 claims 1
- NPEHKMAXIRRIGE-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(pyrazolo[1,5-c]quinazolin-5-ylmethyl)purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3N4N=CC=C4C4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 NPEHKMAXIRRIGE-UHFFFAOYSA-N 0.000 claims 1
- YYCUOVCCKCVCIQ-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-[(11-methylbenzo[b][1,4]benzodiazepin-6-yl)methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4N(C)C4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 YYCUOVCCKCVCIQ-UHFFFAOYSA-N 0.000 claims 1
- SEQPMUCFBUXEKA-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-[(3-methylbenzo[b][1,4]benzoxazepin-6-yl)methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4OC4=CC=C(C)C=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 SEQPMUCFBUXEKA-UHFFFAOYSA-N 0.000 claims 1
- AJGLBCXPISVKSC-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-[(8-methylphenanthridin-6-yl)methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC(C)=CC=C4C4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 AJGLBCXPISVKSC-UHFFFAOYSA-N 0.000 claims 1
- OQQXXYWFEIGADR-UHFFFAOYSA-N 8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-[[3-(trifluoromethyl)-3,4-dihydroisoquinolin-1-yl]methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4CC(N=3)C(F)(F)F)C(=O)C=2N(CC#CC)C=1N1CCCC(N)C1 OQQXXYWFEIGADR-UHFFFAOYSA-N 0.000 claims 1
- WAYVDLYVFNWYST-QDLOVBKTSA-N 8-[(3R)-3-aminopiperidin-1-yl]-7-[(E)-but-2-enyl]-3-methyl-1-[(2-oxo-1,3-dihydro-1,4-benzodiazepin-5-yl)methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4NC(=O)CN=3)C(=O)C=2N(C/C=C/C)C=1N1CCC[C@@H](N)C1 WAYVDLYVFNWYST-QDLOVBKTSA-N 0.000 claims 1
- XWEOHAJQVMIKGZ-LJQANCHMSA-N 8-[(3r)-3-aminopiperidin-1-yl]-1-(benzo[b][1,4]benzoxazepin-6-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4OC4=CC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 XWEOHAJQVMIKGZ-LJQANCHMSA-N 0.000 claims 1
- AXEHMQLMYWEERM-GOSISDBHSA-N 8-[(3r)-3-aminopiperidin-1-yl]-1-(benzo[c][1,5]naphthyridin-6-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4C4=NC=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 AXEHMQLMYWEERM-GOSISDBHSA-N 0.000 claims 1
- MYLRLUAHSYVIEO-LJQANCHMSA-N 8-[(3r)-3-aminopiperidin-1-yl]-1-(benzo[f]quinoxalin-6-ylmethyl)-7-but-2-ynyl-3-methylpurine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4C4=NC=CN=C4C=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 MYLRLUAHSYVIEO-LJQANCHMSA-N 0.000 claims 1
- IIFWKNLPZOLJAK-HXUWFJFHSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-cyclopropyl-1-(phenanthridin-6-ylmethyl)purine-2,6-dione Chemical compound O=C1N(CC=2C3=CC=CC=C3C3=CC=CC=C3N=2)C(=O)C=2N(CC#CC)C(N3C[C@H](N)CCC3)=NC=2N1C1CC1 IIFWKNLPZOLJAK-HXUWFJFHSA-N 0.000 claims 1
- LJNCRERRKMEOMA-GOSISDBHSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-1-(1h-perimidin-2-ylmethyl)purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3NC=4C=CC=C5C=CC=C(C=45)N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 LJNCRERRKMEOMA-GOSISDBHSA-N 0.000 claims 1
- HRIOVHDWMBVNRH-HXUWFJFHSA-N 8-[(3r)-3-aminopiperidin-1-yl]-7-but-2-ynyl-3-methyl-1-[(1-methylphenanthridin-6-yl)methyl]purine-2,6-dione Chemical compound N=1C=2N(C)C(=O)N(CC=3C4=CC=CC=C4C4=C(C)C=CC=C4N=3)C(=O)C=2N(CC#CC)C=1N1CCC[C@@H](N)C1 HRIOVHDWMBVNRH-HXUWFJFHSA-N 0.000 claims 1
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| JP6374862B2 (ja) | 2012-05-24 | 2018-08-15 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 自己免疫性糖尿病、特に、ｌａｄａの治療に使用するためのｄｐｐ−４阻害剤としてのキサンチン誘導体 |
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Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2001268958B2 (en) * | 2000-07-04 | 2006-03-09 | Novo Nordisk A/S | Heterocyclic compounds, which are inhibitors of the enzyme dpp-iv |
| DE10117803A1 (de) | 2001-04-10 | 2002-10-24 | Boehringer Ingelheim Pharma | Xanthinderivate, deren Herstellung und deren Verwendung als Arzneimittel |
| DE10109021A1 (de) * | 2001-02-24 | 2002-09-05 | Boehringer Ingelheim Pharma | Xanthinderivate, deren Herstellung und deren Verwendung als Arzneimittel |
| EP1368349B1 (de) * | 2001-02-24 | 2007-02-14 | Boehringer Ingelheim Pharma GmbH & Co.KG | Xanthinderivate, deren herstellung und deren verwendung als arzneimittel |
| AU2002331311A1 (en) * | 2001-09-19 | 2003-04-01 | Novo Nordisk A/S | Heterocyclic compounds that are inhibitors of the enzyme dpp-iv |
| ES2339112T3 (es) * | 2002-08-21 | 2010-05-17 | BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG | 8-(3-amino-piperidin-1-il)-xantinas,su preparacion y su uso como medicamentos. |
| DE10251927A1 (de) * | 2002-11-08 | 2004-05-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Xanthinderivate, deren Herstellung und deren Verwendung als Arzneimittel |
-
2002
- 2002-11-08 DE DE10251927A patent/DE10251927A1/de not_active Withdrawn
-
2003
- 2003-11-03 EP EP10158963A patent/EP2228375A1/de not_active Withdrawn
- 2003-11-03 ES ES03788995T patent/ES2346432T3/es not_active Expired - Lifetime
- 2003-11-03 PT PT03788995T patent/PT1562946E/pt unknown
- 2003-11-03 AT AT03788995T patent/ATE469152T1/de active
- 2003-11-03 CA CA2505389A patent/CA2505389C/en not_active Expired - Fee Related
- 2003-11-03 DK DK03788995.3T patent/DK1562946T5/da active
- 2003-11-03 EP EP03788995A patent/EP1562946B1/de not_active Expired - Lifetime
- 2003-11-03 AU AU2003293649A patent/AU2003293649A1/en not_active Abandoned
- 2003-11-03 JP JP2004548847A patent/JP4832758B2/ja not_active Expired - Fee Related
- 2003-11-03 WO PCT/EP2003/012198 patent/WO2004041820A1/de not_active Ceased
- 2003-11-03 DE DE50312747T patent/DE50312747D1/de not_active Expired - Lifetime
- 2003-11-03 SI SI200331855T patent/SI1562946T1/sl unknown
- 2003-11-06 PE PE2003001124A patent/PE20040829A1/es not_active Application Discontinuation
- 2003-11-07 AR ARP030104097A patent/AR043060A1/es unknown
- 2003-11-07 TW TW092131252A patent/TW200512210A/zh unknown
- 2003-11-07 UY UY28069A patent/UY28069A1/es not_active Application Discontinuation
-
2010
- 2010-08-20 CY CY20101100774T patent/CY1110749T1/el unknown
- 2010-10-19 JP JP2010234795A patent/JP2011012085A/ja not_active Withdrawn
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