NO328713B1 - Tienopyrimidindioner, fremgangsmate til fremstilling derav, farmasoytisk sammensetning inneholdende slike, samt deres anvendelse ved terapi - Google Patents
Tienopyrimidindioner, fremgangsmate til fremstilling derav, farmasoytisk sammensetning inneholdende slike, samt deres anvendelse ved terapi Download PDFInfo
- Publication number
- NO328713B1 NO328713B1 NO20040364A NO20040364A NO328713B1 NO 328713 B1 NO328713 B1 NO 328713B1 NO 20040364 A NO20040364 A NO 20040364A NO 20040364 A NO20040364 A NO 20040364A NO 328713 B1 NO328713 B1 NO 328713B1
- Authority
- NO
- Norway
- Prior art keywords
- methyl
- dione
- pyrimidine
- ylcarbonyl
- thieno
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 202
- 238000002360 preparation method Methods 0.000 title claims description 10
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 8
- 238000002560 therapeutic procedure Methods 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 364
- -1 isoxazolidin-2-ylcarbonyl Chemical group 0.000 claims description 229
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 107
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 71
- 125000000217 alkyl group Chemical group 0.000 claims description 58
- 229910052757 nitrogen Inorganic materials 0.000 claims description 57
- JGOOQALRLGHKIY-UHFFFAOYSA-N 1h-thieno[2,3-d]pyrimidine-2,4-dione Chemical compound O=C1NC(=O)NC2=C1C=CS2 JGOOQALRLGHKIY-UHFFFAOYSA-N 0.000 claims description 47
- 150000003839 salts Chemical class 0.000 claims description 45
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 42
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 35
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 claims description 26
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 26
- 125000004043 oxo group Chemical group O=* 0.000 claims description 26
- 125000001424 substituent group Chemical group 0.000 claims description 26
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 19
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
- 125000004122 cyclic group Chemical group 0.000 claims description 16
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 16
- 125000004076 pyridyl group Chemical group 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 125000005842 heteroatom Chemical group 0.000 claims description 14
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000000464 thioxo group Chemical group S=* 0.000 claims description 14
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 13
- 238000011282 treatment Methods 0.000 claims description 13
- 230000002441 reversible effect Effects 0.000 claims description 12
- 125000006413 ring segment Chemical group 0.000 claims description 12
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 11
- 125000004385 trihaloalkyl group Chemical group 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 125000002883 imidazolyl group Chemical group 0.000 claims description 9
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 9
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 9
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 9
- 239000003814 drug Substances 0.000 claims description 8
- 125000001041 indolyl group Chemical group 0.000 claims description 8
- 125000005493 quinolyl group Chemical group 0.000 claims description 8
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000003786 synthesis reaction Methods 0.000 claims description 6
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 5
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 5
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 5
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 5
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims description 4
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims description 4
- 206010062016 Immunosuppression Diseases 0.000 claims description 4
- 239000002671 adjuvant Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 230000001506 immunosuppresive effect Effects 0.000 claims description 4
- 208000023504 respiratory system disease Diseases 0.000 claims description 4
- CIISBYKBBMFLEZ-UHFFFAOYSA-N 1,2-oxazolidine Chemical compound C1CNOC1 CIISBYKBBMFLEZ-UHFFFAOYSA-N 0.000 claims description 3
- GMUYBYWHRGVEIG-INIZCTEOSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-[(2-propylbenzimidazol-1-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound CCCC1=NC2=CC=CC=C2N1CC=1SC=2N(CC(C)C)C(=O)N(C)C(=O)C=2C=1C(=O)N1C[C@H](O)CO1 GMUYBYWHRGVEIG-INIZCTEOSA-N 0.000 claims description 3
- XIXMTIJQLLRJIJ-AWEZNQCLSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(5-methyl-3-propan-2-yl-1h-pyrazol-4-yl)methyl]-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CC1=C(C)NN=C1C(C)C XIXMTIJQLLRJIJ-AWEZNQCLSA-N 0.000 claims description 3
- GSGSGKQSENPYHG-VIFPVBQESA-N 6-[(2-bromo-4,5-dichloroimidazol-1-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CN1C(Br)=NC(Cl)=C1Cl GSGSGKQSENPYHG-VIFPVBQESA-N 0.000 claims description 3
- NWDXTHRUMCBLPT-IBGZPJMESA-N 6-[(3,5-dimethyl-1-phenylpyrazol-4-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CC(=C1C)C(C)=NN1C1=CC=CC=C1 NWDXTHRUMCBLPT-IBGZPJMESA-N 0.000 claims description 3
- FXYDHGALICIHIR-ZDUSSCGKSA-N 6-[(3,5-dimethyl-1h-pyrazol-4-yl)methyl]-3-ethyl-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-1-propan-2-ylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(CC)C(=O)N(C(C)C)C=2SC=1CC=1C(C)=NNC=1C FXYDHGALICIHIR-ZDUSSCGKSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 239000012453 solvate Substances 0.000 claims description 3
- MODGZFYFFURRKI-NSHDSACASA-N 1-ethyl-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-oxo-1,3-benzothiazol-3-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC)C=2SC(CN2C(SC3=CC=CC=C32)=O)=C1C(=O)N1C[C@H](O)CO1 MODGZFYFFURRKI-NSHDSACASA-N 0.000 claims description 2
- JWADHAVOUUUADB-AWEZNQCLSA-N 1-ethyl-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-propylbenzimidazol-1-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound CCCC1=NC2=CC=CC=C2N1CC=1SC=2N(CC)C(=O)N(C)C(=O)C=2C=1C(=O)N1C[C@H](O)CO1 JWADHAVOUUUADB-AWEZNQCLSA-N 0.000 claims description 2
- SVOCLWUDDWXHFW-UHFFFAOYSA-N 2-methylsulfanyl-1h-imidazole Chemical compound CSC1=NC=CN1 SVOCLWUDDWXHFW-UHFFFAOYSA-N 0.000 claims description 2
- XEVQNMOABVOAGK-OAHLLOKOSA-N 5-[(4r)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-methyl-1h-indol-3-yl)methyl]-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CC=2C3=CC=CC=C3NC=2C)=C1C(=O)N1C[C@@H](O)CO1 XEVQNMOABVOAGK-OAHLLOKOSA-N 0.000 claims description 2
- SYABSTPXYAKTOJ-AWEZNQCLSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-[(1,3,5-trimethylpyrazol-4-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CC=1C(C)=NN(C)C=1C SYABSTPXYAKTOJ-AWEZNQCLSA-N 0.000 claims description 2
- VFHHJCWOWISPED-KRWDZBQOSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-[(2-methylquinolin-4-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CC=2C3=CC=CC=C3N=C(C)C=2)=C1C(=O)N1C[C@H](O)CO1 VFHHJCWOWISPED-KRWDZBQOSA-N 0.000 claims description 2
- KWUIRMHYFXHDFM-LBPRGKRZSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-[(2-methylsulfanylimidazol-1-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound CSC1=NC=CN1CC1=C(C(=O)N2OC[C@@H](O)C2)C(C(=O)N(C)C(=O)N2CC(C)C)=C2S1 KWUIRMHYFXHDFM-LBPRGKRZSA-N 0.000 claims description 2
- IBBQWKIRDFVRSO-ZDUSSCGKSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-[(2-oxo-1,3-benzothiazol-3-yl)methyl]thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CN2C(SC3=CC=CC=C32)=O)=C1C(=O)N1C[C@H](O)CO1 IBBQWKIRDFVRSO-ZDUSSCGKSA-N 0.000 claims description 2
- HUXYVUKYQUIKAF-AWEZNQCLSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-(2-methyl-1h-indole-3-carbonyl)-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(C(=O)C=2C3=CC=CC=C3NC=2C)=C1C(=O)N1C[C@H](O)CO1 HUXYVUKYQUIKAF-AWEZNQCLSA-N 0.000 claims description 2
- YVJYZPRWQVUGQK-LBPRGKRZSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-oxo-3h-benzimidazol-1-yl)methyl]-1-propan-2-ylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(C(C)C)C=2SC(CN2C(NC3=CC=CC=C32)=O)=C1C(=O)N1C[C@H](O)CO1 YVJYZPRWQVUGQK-LBPRGKRZSA-N 0.000 claims description 2
- JWSHRUJJZBNBBD-NSHDSACASA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-oxo-[1,3]thiazolo[5,4-b]pyridin-1-yl)methyl]-1-propan-2-ylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(C(C)C)C=2SC(CN2C(SC3=NC=CC=C32)=O)=C1C(=O)N1C[C@H](O)CO1 JWSHRUJJZBNBBD-NSHDSACASA-N 0.000 claims description 2
- CYXVQFUBNAVJSY-KRWDZBQOSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(5-methyl-3-phenyl-1h-pyrazol-4-yl)methyl]-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CC1=C(C)NN=C1C1=CC=CC=C1 CYXVQFUBNAVJSY-KRWDZBQOSA-N 0.000 claims description 2
- RBMGZPYCDQPSLS-AWEZNQCLSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[[2-(methylamino)benzimidazol-1-yl]methyl]-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound CNC1=NC2=CC=CC=C2N1CC=1SC=2N(CC(C)C)C(=O)N(C)C(=O)C=2C=1C(=O)N1C[C@H](O)CO1 RBMGZPYCDQPSLS-AWEZNQCLSA-N 0.000 claims description 2
- HAFALVDBJMSQDY-ZDUSSCGKSA-N 5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-6-[[2-(methylamino)benzimidazol-1-yl]methyl]-1-propan-2-ylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound CNC1=NC2=CC=CC=C2N1CC=1SC=2N(C(C)C)C(=O)N(C)C(=O)C=2C=1C(=O)N1C[C@H](O)CO1 HAFALVDBJMSQDY-ZDUSSCGKSA-N 0.000 claims description 2
- LATSXWIPGFHYDG-ZDUSSCGKSA-N 6-(benzotriazol-1-ylmethyl)-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CN2C3=CC=CC=C3N=N2)=C1C(=O)N1C[C@H](O)CO1 LATSXWIPGFHYDG-ZDUSSCGKSA-N 0.000 claims description 2
- MNNWRXMQFXOPNJ-LBPRGKRZSA-N 6-(benzotriazol-1-ylmethyl)-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-propan-2-ylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(C(C)C)C=2SC(CN2C3=CC=CC=C3N=N2)=C1C(=O)N1C[C@H](O)CO1 MNNWRXMQFXOPNJ-LBPRGKRZSA-N 0.000 claims description 2
- ZHWJLKCQMOWILZ-LBPRGKRZSA-N 6-[(2-aminobenzimidazol-1-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-propylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CCC)C=2SC(CN2C3=CC=CC=C3N=C2N)=C1C(=O)N1C[C@H](O)CO1 ZHWJLKCQMOWILZ-LBPRGKRZSA-N 0.000 claims description 2
- RECMMXWFDZIIOE-HNNXBMFYSA-N 6-[(2-ethylbenzimidazol-1-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound CCC1=NC2=CC=CC=C2N1CC=1SC=2N(CC(C)C)C(=O)N(C)C(=O)C=2C=1C(=O)N1C[C@H](O)CO1 RECMMXWFDZIIOE-HNNXBMFYSA-N 0.000 claims description 2
- UAXYKEAANLHJGN-SFHVURJKSA-N 6-[(3,5-dimethyl-1-phenylpyrazol-4-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-propylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CCC)C=2SC=1CC(=C1C)C(C)=NN1C1=CC=CC=C1 UAXYKEAANLHJGN-SFHVURJKSA-N 0.000 claims description 2
- ISIVOJWVBJIOFM-ZDUSSCGKSA-N 6-[(3,5-dimethyl-1h-pyrazol-4-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CC=1C(C)=NNC=1C ISIVOJWVBJIOFM-ZDUSSCGKSA-N 0.000 claims description 2
- QKBZODOPLHOHSA-LBPRGKRZSA-N 6-[(3,5-dimethyl-1h-pyrazol-4-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-propylthieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CCC)C=2SC=1CC=1C(C)=NNC=1C QKBZODOPLHOHSA-LBPRGKRZSA-N 0.000 claims description 2
- COYABIKHBNKNNW-VIFPVBQESA-N 6-[(4,5-dichloro-2-oxo-1,3-thiazol-3-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C([C@@H](O)C1)ON1C(=O)C=1C=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC=1CN1C(Cl)=C(Cl)SC1=O COYABIKHBNKNNW-VIFPVBQESA-N 0.000 claims description 2
- PTHUFRQNBGYBIG-NSHDSACASA-N 6-[(5,6-difluoro-2-oxo-3h-benzimidazol-1-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CN2C(NC3=CC(F)=C(F)C=C32)=O)=C1C(=O)N1C[C@H](O)CO1 PTHUFRQNBGYBIG-NSHDSACASA-N 0.000 claims description 2
- GARDAKJSPJYBGR-INIZCTEOSA-N 6-[(6-fluoroquinolin-4-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CC=2C3=CC(F)=CC=C3N=CC=2)=C1C(=O)N1C[C@H](O)CO1 GARDAKJSPJYBGR-INIZCTEOSA-N 0.000 claims description 2
- VGGIJLVSICXJBM-HNNXBMFYSA-N 6-[(8-fluoroquinolin-4-yl)methyl]-5-[(4s)-4-hydroxy-1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4-dione Chemical compound C1=2C(=O)N(C)C(=O)N(CC(C)C)C=2SC(CC=2C3=CC=CC(F)=C3N=CC=2)=C1C(=O)N1C[C@H](O)CO1 VGGIJLVSICXJBM-HNNXBMFYSA-N 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 230000000414 obstructive effect Effects 0.000 claims description 2
- UCKMFSQOBOTJJB-KBDARXMYSA-N (5s)-6-[(4,5-dichloro-2-methylimidazol-1-yl)methyl]-5-(4-hydroxy-1,2-oxazolidine-2-carbonyl)-3-methyl-1-propan-2-yl-4,6-dihydro-2h-thieno[2,3-d]pyrimidine-5-carboxamide Chemical compound CC(C)N1CN(C)CC([C@]2(C(N)=O)C(=O)N3OCC(O)C3)=C1SC2CN1C(C)=NC(Cl)=C1Cl UCKMFSQOBOTJJB-KBDARXMYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
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GBGB0118479.5A GB0118479D0 (en) | 2001-07-28 | 2001-07-28 | Novel compounds |
PCT/GB2002/003399 WO2003011868A1 (en) | 2001-07-28 | 2002-07-24 | Thienopyrimidinediones and their use in the modulation of autoimmune disease |
Publications (2)
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NO20040364L NO20040364L (no) | 2004-03-29 |
NO328713B1 true NO328713B1 (no) | 2010-05-03 |
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NO20040364A NO328713B1 (no) | 2001-07-28 | 2004-01-27 | Tienopyrimidindioner, fremgangsmate til fremstilling derav, farmasoytisk sammensetning inneholdende slike, samt deres anvendelse ved terapi |
Country Status (25)
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US (2) | US7384950B2 (ru) |
EP (1) | EP1414825B9 (ru) |
JP (1) | JP4456364B2 (ru) |
KR (1) | KR100897469B1 (ru) |
CN (1) | CN1324033C (ru) |
AR (1) | AR038000A1 (ru) |
AT (1) | ATE374204T1 (ru) |
AU (1) | AU2002319469B2 (ru) |
BR (1) | BR0211262A (ru) |
CA (1) | CA2453274A1 (ru) |
DE (1) | DE60222671T2 (ru) |
ES (1) | ES2292784T3 (ru) |
GB (1) | GB0118479D0 (ru) |
HK (1) | HK1065785A1 (ru) |
HU (1) | HUP0402336A3 (ru) |
IL (2) | IL159785A0 (ru) |
IS (1) | IS2598B (ru) |
MX (1) | MXPA04000677A (ru) |
MY (1) | MY138145A (ru) |
NO (1) | NO328713B1 (ru) |
NZ (1) | NZ530495A (ru) |
PL (1) | PL211351B1 (ru) |
RU (1) | RU2294937C9 (ru) |
WO (1) | WO2003011868A1 (ru) |
ZA (1) | ZA200400574B (ru) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
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SE9801399D0 (sv) | 1998-04-21 | 1998-04-21 | Astra Pharma Prod | Method and apparatus for filling containers |
GB0117583D0 (en) * | 2001-07-19 | 2001-09-12 | Astrazeneca Ab | Novel compounds |
GB0118479D0 (en) * | 2001-07-28 | 2001-09-19 | Astrazeneca Ab | Novel compounds |
US7718802B2 (en) | 2001-08-10 | 2010-05-18 | Palatin Technologies, Inc. | Substituted melanocortin receptor-specific piperazine compounds |
US7456184B2 (en) | 2003-05-01 | 2008-11-25 | Palatin Technologies Inc. | Melanocortin receptor-specific compounds |
US7732451B2 (en) | 2001-08-10 | 2010-06-08 | Palatin Technologies, Inc. | Naphthalene-containing melanocortin receptor-specific small molecule |
EP1425029A4 (en) | 2001-08-10 | 2006-06-07 | Palatin Technologies Inc | PEPTIDOMIMETICS OF BIOLOGICALLY ACTIVE METALLOPEPTIDES |
US7655658B2 (en) | 2001-08-10 | 2010-02-02 | Palatin Technologies, Inc. | Thieno [2,3-D]pyrimidine-2,4-dione melanocortin-specific compounds |
DE60304718T2 (de) | 2002-08-06 | 2007-04-26 | Astrazeneca Ab | Kondensierte pyridine und pyrimidine mit tie2 (tek) aktivität |
US6890923B2 (en) * | 2002-12-16 | 2005-05-10 | Astrazeneca Ab | Compounds |
US7393854B2 (en) * | 2003-01-17 | 2008-07-01 | Astrazeneca Ab | Thienopyrimidinedinones and their use in modulation of autoimmune disease |
SE0300120D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
SE0300119D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
CA2518398A1 (en) * | 2003-03-10 | 2004-09-23 | Schering Corporation | Heterocyclic kinase inhibitors: methods of use and synthesis |
US7968548B2 (en) * | 2003-05-01 | 2011-06-28 | Palatin Technologies, Inc. | Melanocortin receptor-specific piperazine compounds with diamine groups |
US7727990B2 (en) | 2003-05-01 | 2010-06-01 | Palatin Technologies, Inc. | Melanocortin receptor-specific piperazine and keto-piperazine compounds |
US7727991B2 (en) | 2003-05-01 | 2010-06-01 | Palatin Technologies, Inc. | Substituted melanocortin receptor-specific single acyl piperazine compounds |
SI1696920T1 (sl) | 2003-12-19 | 2015-02-27 | Plexxikon Inc. | Spojine in postopki za razvoj modulatorjev ret |
US7550602B1 (en) | 2004-01-14 | 2009-06-23 | Palatin Technologies, Inc. | Small molecule compositions for sexual dysfunction |
US7709484B1 (en) | 2004-04-19 | 2010-05-04 | Palatin Technologies, Inc. | Substituted melanocortin receptor-specific piperazine compounds |
US7498342B2 (en) | 2004-06-17 | 2009-03-03 | Plexxikon, Inc. | Compounds modulating c-kit activity |
US7732472B2 (en) * | 2004-08-18 | 2010-06-08 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
CA2608733A1 (en) | 2005-05-17 | 2007-02-01 | Plexxikon, Inc. | Pyrrol (2,3-b) pyridine derivatives protein kinase inhibitors |
EP3088400A1 (en) | 2005-06-22 | 2016-11-02 | Plexxikon Inc. | Pyrrolo[2,3-b]pyridine derivatives as protein kinase inhibitors |
US7834017B2 (en) | 2006-08-11 | 2010-11-16 | Palatin Technologies, Inc. | Diamine-containing, tetra-substituted piperazine compounds having identical 1- and 4-substituents |
WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
RU2341527C1 (ru) * | 2007-07-17 | 2008-12-20 | Общество С Ограниченной Ответственностью "Исследовательский Институт Химического Разнообразия" | Аннелированные азагетероциклы, включающие пиримидиновый фрагмент, способ их получения и ингибиторы pi3k киназ |
RU2345996C1 (ru) * | 2007-07-17 | 2009-02-10 | Андрей Александрович Иващенко | Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения |
MX2010000617A (es) | 2007-07-17 | 2010-05-17 | Plexxikon Inc | Compuestos y metodos para modulacion de cinasa, e indicaciones de estos. |
AR070220A1 (es) * | 2008-01-22 | 2010-03-25 | Boehringer Ingelheim Int | Amino-bencimidazoles sustituidos medicamentos que comprenden dicho compuestos, uso y metodos de fabricacion de los mismos |
PT2411395E (pt) * | 2009-03-23 | 2013-06-06 | Glenmark Pharmaceuticals Sa | Derivados de furopirimidinadiona como moduladores de trpa1 |
SG173178A1 (en) | 2009-04-03 | 2011-09-29 | Hoffmann La Roche | Propane- i-sulfonic acid {3- [5- (4 -chloro-phenyl) -1h-pyrrolo [2, 3-b] pyridine-3-carbonyl] -2, 4-difluoro-pheny l } -amide compositions and uses thereof |
JP2013510166A (ja) | 2009-11-06 | 2013-03-21 | プレキシコン インコーポレーテッド | キナーゼ調節のための化合物、方法およびその適用 |
RS58455B1 (sr) | 2011-02-07 | 2019-04-30 | Plexxikon Inc | Jedinjenja i postupci za modulaciju kinaze, i indikacije za njih |
TWI558702B (zh) | 2011-02-21 | 2016-11-21 | 普雷辛肯公司 | 醫藥活性物質的固態形式 |
JP5990980B2 (ja) * | 2012-04-02 | 2016-09-14 | 大日本印刷株式会社 | オランザピンの中間体の製造方法 |
US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
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US6469014B1 (en) * | 1997-05-28 | 2002-10-22 | Astrazeneca Ab | Thieno[2,3-d] pyrimidinediones, their preparation and use in therapy |
SE9702001D0 (sv) * | 1997-05-28 | 1997-05-28 | Astra Pharma Prod | Novel compounds |
JP2001525413A (ja) | 1997-12-05 | 2001-12-11 | アストラゼネカ ユーケイ リミテッド | 新規化合物 |
US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
ES2211161T3 (es) | 1998-08-28 | 2004-07-01 | Astrazeneca Ab | Tieno(2,3-d)pirimidindionas novedosas, procedimiento para su preparacion y uso de las mismas en terapia. |
GB0117583D0 (en) * | 2001-07-19 | 2001-09-12 | Astrazeneca Ab | Novel compounds |
GB0118479D0 (en) * | 2001-07-28 | 2001-09-19 | Astrazeneca Ab | Novel compounds |
US7393854B2 (en) | 2003-01-17 | 2008-07-01 | Astrazeneca Ab | Thienopyrimidinedinones and their use in modulation of autoimmune disease |
SE0300120D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
SE0300119D0 (sv) * | 2003-01-17 | 2003-01-17 | Astrazeneca Ab | Novel compounds |
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2001
- 2001-07-28 GB GBGB0118479.5A patent/GB0118479D0/en not_active Ceased
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2002
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- 2002-07-24 ES ES02749055T patent/ES2292784T3/es not_active Expired - Lifetime
- 2002-07-24 DE DE60222671T patent/DE60222671T2/de not_active Expired - Lifetime
- 2002-07-24 AT AT02749055T patent/ATE374204T1/de not_active IP Right Cessation
- 2002-07-24 CN CNB028152506A patent/CN1324033C/zh not_active Expired - Fee Related
- 2002-07-24 BR BR0211262-0A patent/BR0211262A/pt not_active IP Right Cessation
- 2002-07-24 AU AU2002319469A patent/AU2002319469B2/en not_active Ceased
- 2002-07-24 CA CA002453274A patent/CA2453274A1/en not_active Abandoned
- 2002-07-24 PL PL369232A patent/PL211351B1/pl not_active IP Right Cessation
- 2002-07-24 IL IL15978502A patent/IL159785A0/xx unknown
- 2002-07-24 MX MXPA04000677A patent/MXPA04000677A/es active IP Right Grant
- 2002-07-24 KR KR1020047001192A patent/KR100897469B1/ko not_active IP Right Cessation
- 2002-07-24 JP JP2003517059A patent/JP4456364B2/ja not_active Expired - Fee Related
- 2002-07-24 RU RU2004102392/04A patent/RU2294937C9/ru not_active IP Right Cessation
- 2002-07-24 US US10/483,162 patent/US7384950B2/en not_active Expired - Fee Related
- 2002-07-24 EP EP02749055A patent/EP1414825B9/en not_active Expired - Lifetime
- 2002-07-24 NZ NZ530495A patent/NZ530495A/en not_active IP Right Cessation
- 2002-07-24 WO PCT/GB2002/003399 patent/WO2003011868A1/en active IP Right Grant
- 2002-07-26 AR ARP020102842A patent/AR038000A1/es active IP Right Grant
- 2002-07-26 MY MYPI20022835A patent/MY138145A/en unknown
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2004
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- 2004-01-19 IS IS7118A patent/IS2598B/is unknown
- 2004-01-26 ZA ZA200400574A patent/ZA200400574B/en unknown
- 2004-01-27 NO NO20040364A patent/NO328713B1/no not_active IP Right Cessation
- 2004-10-28 HK HK04108484A patent/HK1065785A1/xx not_active IP Right Cessation
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2008
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