NO331977B1 - 2,4-di(fenylamino)pyrimidiner, fremgangsmate for fremstilling derav, anvendelse derav samt farmasoytisk preparat innholdende en slik forbindelse - Google Patents
2,4-di(fenylamino)pyrimidiner, fremgangsmate for fremstilling derav, anvendelse derav samt farmasoytisk preparat innholdende en slik forbindelse Download PDFInfo
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- NO331977B1 NO331977B1 NO20054726A NO20054726A NO331977B1 NO 331977 B1 NO331977 B1 NO 331977B1 NO 20054726 A NO20054726 A NO 20054726A NO 20054726 A NO20054726 A NO 20054726A NO 331977 B1 NO331977 B1 NO 331977B1
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- 238000002360 preparation method Methods 0.000 title claims abstract description 41
- 150000001875 compounds Chemical class 0.000 title claims description 212
- 238000000034 method Methods 0.000 title abstract description 43
- 239000008194 pharmaceutical composition Substances 0.000 title abstract description 9
- GKFFFOLFBJUEFN-UHFFFAOYSA-N 2-n,4-n-diphenylpyrimidine-2,4-diamine Chemical class C=1C=NC(NC=2C=CC=CC=2)=NC=1NC1=CC=CC=C1 GKFFFOLFBJUEFN-UHFFFAOYSA-N 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 27
- 201000010099 disease Diseases 0.000 claims abstract description 18
- 208000026278 immune system disease Diseases 0.000 claims abstract description 7
- 230000001613 neoplastic effect Effects 0.000 claims abstract description 7
- 208000027866 inflammatory disease Diseases 0.000 claims abstract description 5
- -1 hydroxy, amino, substituted amino Chemical group 0.000 claims description 91
- 229910052739 hydrogen Inorganic materials 0.000 claims description 45
- 239000001257 hydrogen Substances 0.000 claims description 45
- 150000003839 salts Chemical class 0.000 claims description 41
- 125000000623 heterocyclic group Chemical group 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 102000016621 Focal Adhesion Protein-Tyrosine Kinases Human genes 0.000 claims description 29
- 108010067715 Focal Adhesion Protein-Tyrosine Kinases Proteins 0.000 claims description 29
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 25
- 229910052736 halogen Inorganic materials 0.000 claims description 25
- 150000002367 halogens Chemical class 0.000 claims description 25
- 206010028980 Neoplasm Diseases 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 150000002431 hydrogen Chemical class 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 18
- 125000005842 heteroatom Chemical group 0.000 claims description 18
- 230000005764 inhibitory process Effects 0.000 claims description 17
- 239000004480 active ingredient Substances 0.000 claims description 16
- 239000000460 chlorine Substances 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 229910052717 sulfur Inorganic materials 0.000 claims description 14
- 229920006395 saturated elastomer Polymers 0.000 claims description 13
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 12
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 10
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
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- 238000004519 manufacturing process Methods 0.000 claims description 8
- 230000001404 mediated effect Effects 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
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- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
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- 125000003277 amino group Chemical group 0.000 claims description 5
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
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- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims description 2
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 2
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- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 210000004443 dendritic cell Anatomy 0.000 claims description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
- 210000003734 kidney Anatomy 0.000 claims description 2
- 210000004072 lung Anatomy 0.000 claims description 2
- 210000002540 macrophage Anatomy 0.000 claims description 2
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 2
- 210000001672 ovary Anatomy 0.000 claims description 2
- 210000000496 pancreas Anatomy 0.000 claims description 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- ZWMDEVPYVGQJHU-UHFFFAOYSA-N 2-[[5-bromo-2-(2-methoxy-4-morpholin-4-ylanilino)pyrimidin-4-yl]amino]-n,n-dimethylbenzenesulfonamide Chemical compound COC1=CC(N2CCOCC2)=CC=C1NC(N=1)=NC=C(Br)C=1NC1=CC=CC=C1S(=O)(=O)N(C)C ZWMDEVPYVGQJHU-UHFFFAOYSA-N 0.000 claims 1
- JHMBTUMIVBSJFS-UHFFFAOYSA-N 2-methyl-3h-isoindol-1-one Chemical compound C1=CC=C2C(=O)N(C)CC2=C1 JHMBTUMIVBSJFS-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
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- A—HUMAN NECESSITIES
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- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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GBGB0305929.2A GB0305929D0 (en) | 2003-03-14 | 2003-03-14 | Organic compounds |
GB0319227A GB0319227D0 (en) | 2003-08-15 | 2003-08-15 | Organic compounds |
GB0322370A GB0322370D0 (en) | 2003-09-24 | 2003-09-24 | Organic compounds |
PCT/EP2004/002616 WO2004080980A1 (en) | 2003-03-14 | 2004-03-12 | 2, 4- di (phenylamino) pyrimidines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders |
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NO20054726D0 NO20054726D0 (no) | 2005-10-13 |
NO20054726L NO20054726L (no) | 2005-12-08 |
NO331977B1 true NO331977B1 (no) | 2012-05-14 |
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NO20054726A NO331977B1 (no) | 2003-03-14 | 2005-10-13 | 2,4-di(fenylamino)pyrimidiner, fremgangsmate for fremstilling derav, anvendelse derav samt farmasoytisk preparat innholdende en slik forbindelse |
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US (2) | US7964592B2 (zh) |
EP (2) | EP2275413B1 (zh) |
JP (1) | JP4796487B2 (zh) |
KR (1) | KR101148261B1 (zh) |
CN (2) | CN1788001B (zh) |
AT (1) | ATE497495T1 (zh) |
AU (1) | AU2004220338B2 (zh) |
BR (2) | BRPI0408347B8 (zh) |
CA (1) | CA2518932C (zh) |
CY (1) | CY1114238T1 (zh) |
DE (1) | DE602004031287D1 (zh) |
DK (1) | DK2275413T3 (zh) |
EC (1) | ECSP056019A (zh) |
ES (1) | ES2409885T3 (zh) |
GB (1) | GB0305929D0 (zh) |
IL (1) | IL170546A (zh) |
IS (1) | IS2961B (zh) |
MA (1) | MA27668A1 (zh) |
MX (1) | MXPA05009883A (zh) |
NO (1) | NO331977B1 (zh) |
NZ (1) | NZ542219A (zh) |
PL (2) | PL2275413T3 (zh) |
PT (2) | PT1606265E (zh) |
SI (1) | SI2275413T1 (zh) |
TN (1) | TNSN05225A1 (zh) |
WO (1) | WO2004080980A1 (zh) |
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2005
- 2005-08-29 IL IL170546A patent/IL170546A/en active IP Right Grant
- 2005-09-13 TN TNP2005000225A patent/TNSN05225A1/en unknown
- 2005-09-14 EC EC2005006019A patent/ECSP056019A/es unknown
- 2005-09-23 MA MA28510A patent/MA27668A1/fr unknown
- 2005-10-06 IS IS8062A patent/IS2961B/is unknown
- 2005-10-13 NO NO20054726A patent/NO331977B1/no unknown
-
2011
- 2011-04-27 US US13/095,760 patent/US8263590B2/en not_active Expired - Fee Related
-
2013
- 2013-05-27 CY CY20131100414T patent/CY1114238T1/el unknown
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