UA80283C2 - Pyrimidyl sulphone amide derivatives as chemokine receptor modulators - Google Patents
Pyrimidyl sulphone amide derivatives as chemokine receptor modulators Download PDFInfo
- Publication number
- UA80283C2 UA80283C2 UAA200500513A UA2005000513A UA80283C2 UA 80283 C2 UA80283 C2 UA 80283C2 UA A200500513 A UAA200500513 A UA A200500513A UA 2005000513 A UA2005000513 A UA 2005000513A UA 80283 C2 UA80283 C2 UA 80283C2
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- UA
- Ukraine
- Prior art keywords
- compound
- hydroxy
- pyrimidin
- amino
- hiat
- Prior art date
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- -1 Pyrimidyl sulphone amide Chemical class 0.000 title claims description 103
- 102000009410 Chemokine receptor Human genes 0.000 title claims description 9
- 108050000299 Chemokine receptor Proteins 0.000 title claims description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 403
- 150000003839 salts Chemical class 0.000 claims abstract description 65
- 150000002148 esters Chemical class 0.000 claims abstract description 59
- 239000012453 solvate Substances 0.000 claims abstract description 39
- 238000011282 treatment Methods 0.000 claims abstract description 32
- 208000006673 asthma Diseases 0.000 claims abstract description 15
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 14
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims abstract description 13
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims abstract description 13
- 201000011510 cancer Diseases 0.000 claims abstract description 13
- 206010039073 rheumatoid arthritis Diseases 0.000 claims abstract description 13
- 201000004681 Psoriasis Diseases 0.000 claims abstract description 12
- 206010039085 Rhinitis allergic Diseases 0.000 claims abstract description 11
- 201000010105 allergic rhinitis Diseases 0.000 claims abstract description 11
- 201000008482 osteoarthritis Diseases 0.000 claims abstract description 11
- 208000001132 Osteoporosis Diseases 0.000 claims abstract description 10
- 208000002551 irritable bowel syndrome Diseases 0.000 claims abstract description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 125
- 238000000034 method Methods 0.000 claims description 92
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- 125000001424 substituent group Chemical group 0.000 claims description 68
- 229910052736 halogen Inorganic materials 0.000 claims description 66
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- 239000002904 solvent Substances 0.000 claims description 59
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- 239000000203 mixture Substances 0.000 claims description 57
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- 238000006243 chemical reaction Methods 0.000 claims description 50
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 36
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- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 claims description 18
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 15
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 8
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- 229910052802 copper Inorganic materials 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 125000002757 morpholinyl group Chemical group 0.000 claims description 8
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims description 8
- 125000002393 azetidinyl group Chemical group 0.000 claims description 7
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- 238000002560 therapeutic procedure Methods 0.000 claims description 7
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- 230000007062 hydrolysis Effects 0.000 claims description 6
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- 125000002950 monocyclic group Chemical group 0.000 claims description 6
- LPPOVVJDAVMOET-UHFFFAOYSA-N pyrrolidine-1-sulfonamide Chemical compound NS(=O)(=O)N1CCCC1 LPPOVVJDAVMOET-UHFFFAOYSA-N 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
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- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- FLKRMXAWABTWSH-UHFFFAOYSA-N piperidine-1-sulfonamide Chemical compound NS(=O)(=O)N1CCCCC1 FLKRMXAWABTWSH-UHFFFAOYSA-N 0.000 claims description 3
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
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- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical group [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 1
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- 102100026933 Myelin-associated neurite-outgrowth inhibitor Human genes 0.000 description 142
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- 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
- C07D239/69—Benzenesulfonamido-pyrimidines
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- C—CHEMISTRY; METALLURGY
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- 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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- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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GBGB0217431.6A GB0217431D0 (en) | 2002-07-27 | 2002-07-27 | Novel compounds |
PCT/GB2003/003175 WO2004011443A1 (en) | 2002-07-27 | 2003-07-23 | Pyrimidyl sulphone amide derivatives as chemokine receptor modulators |
Publications (1)
Publication Number | Publication Date |
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UA80283C2 true UA80283C2 (en) | 2007-09-10 |
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Application Number | Title | Priority Date | Filing Date |
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UAA200500513A UA80283C2 (en) | 2002-07-27 | 2003-07-23 | Pyrimidyl sulphone amide derivatives as chemokine receptor modulators |
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Country | Link |
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US (2) | US7582644B2 (ru) |
EP (1) | EP1527051B1 (ru) |
JP (1) | JP4619782B2 (ru) |
KR (2) | KR101074626B1 (ru) |
CN (1) | CN100345829C (ru) |
AR (1) | AR040700A1 (ru) |
AU (1) | AU2003281684B2 (ru) |
BR (1) | BR0312967A (ru) |
CA (1) | CA2493785C (ru) |
CO (1) | CO5680479A2 (ru) |
EG (1) | EG25893A (ru) |
ES (1) | ES2392965T3 (ru) |
GB (1) | GB0217431D0 (ru) |
HK (1) | HK1076465A1 (ru) |
IL (1) | IL166290A0 (ru) |
IS (1) | IS7697A (ru) |
MX (1) | MXPA05000960A (ru) |
MY (1) | MY139561A (ru) |
NO (1) | NO330531B1 (ru) |
NZ (1) | NZ537914A (ru) |
PL (1) | PL375400A1 (ru) |
RU (1) | RU2342366C2 (ru) |
TW (1) | TWI340038B (ru) |
UA (1) | UA80283C2 (ru) |
WO (1) | WO2004011443A1 (ru) |
ZA (1) | ZA200500791B (ru) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009064938A1 (en) * | 2007-11-16 | 2009-05-22 | Abbott Laboratories | Method of treating arthritis |
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GB0217431D0 (en) * | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
DE60318219T2 (de) | 2002-08-24 | 2009-01-15 | Astrazeneca Ab | PYRIMIDINDERIVATE ALS MODULATOREN DER AKTIVITuT VON CHEMOKINREZEPTOREN |
GB0401269D0 (en) * | 2004-01-21 | 2004-02-25 | Astrazeneca Ab | Compounds |
US7288563B2 (en) | 2004-02-19 | 2007-10-30 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
US7381738B2 (en) | 2004-02-19 | 2008-06-03 | Bristol-Myers Squibb Company | Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity |
US7479496B2 (en) | 2004-02-19 | 2009-01-20 | Bristol-Myers Squibb Company | Substituted spiro azabicyclics as modulators of chemokine receptor activity |
US7230022B2 (en) | 2004-02-19 | 2007-06-12 | Bristol-Myers Squibb Company | Substituted fused bicyclic amines as modulators of chemokine receptor activity |
EP1809624B1 (en) | 2004-08-28 | 2013-11-20 | AstraZeneca AB | Pyrimidine sulphonamide derivatives as chemokine receptor modulators |
US20060178388A1 (en) | 2005-02-04 | 2006-08-10 | Wrobleski Stephen T | Phenyl-substituted pyrimidine compounds useful as kinase inhibitors |
WO2006124744A1 (en) * | 2005-05-16 | 2006-11-23 | Vertex Pharmaceuticals Incorporated | Bicyclic derivatives as modulators of ion channels |
GB0526255D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
HUE035029T2 (en) | 2008-05-21 | 2018-03-28 | Ariad Pharma Inc | Kinase inhibitor phosphorus derivatives |
WO2009151910A2 (en) * | 2008-05-25 | 2009-12-17 | Wyeth | Combination product of receptor tyrosine kinase inhibitor and fatty acid synthase inhibitor for treating cancer |
BRPI0915908A2 (pt) * | 2008-07-16 | 2018-07-10 | Astrazeneca Ab | derivado de pirimidil sulfonamida e seu uso para o tratamento de doenças mediadas por quimiocina |
EP2516416A1 (en) | 2009-12-23 | 2012-10-31 | Ironwood Pharmaceuticals, Inc. | Crth2 modulators |
US20130259830A1 (en) | 2010-07-12 | 2013-10-03 | Ironwood Pharmaceuticals, Inc. | Crth2 modulators |
US20130216552A1 (en) | 2010-07-12 | 2013-08-22 | Ironwood Pharmaceuticals, Inc. | Crth2 modulators |
MY167869A (en) | 2010-07-13 | 2018-09-26 | Astrazeneca Ab | New Crystalline forms of N-[2-[[(2,3-difluorophenyl)methyl]thio]-6-{[(1R, 2S)-2,3-dihydroxy-1-methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide |
JP5999177B2 (ja) | 2011-05-04 | 2016-09-28 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
MY180039A (en) | 2011-07-12 | 2020-11-20 | Astrazeneca Ab | N- (6- ( (2r,3s) -3,4-dihydroxybutan-2-yloxy) -2- (4 - fluorobenzylthio) pyrimidin- 4 - yl) -3- methylazetidine- 1 - sulfonamide as chemokine receptor modulator |
AU2013204563B2 (en) | 2012-05-05 | 2016-05-19 | Takeda Pharmaceutical Company Limited | Compounds for inhibiting cell proliferation in EGFR-driven cancers |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
TW201512171A (zh) | 2013-04-19 | 2015-04-01 | Pfizer Ltd | 化學化合物 |
US9890158B2 (en) | 2015-10-09 | 2018-02-13 | Abbvie S.Á.R.L. | N-sulfonylated pyrazolo[3,4-b]pyridin-6-carboxamides and method of use |
AU2017231832B2 (en) | 2016-03-11 | 2021-11-11 | Ardea Biosciences, Inc. | CXCR-2 inhibitors for treating crystal arthropathy disorders |
GB201807898D0 (en) * | 2018-05-15 | 2018-06-27 | Kancera Ab | New processes and products with increased chiral purity |
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JPS61118372A (ja) | 1984-11-12 | 1986-06-05 | Nippon Mektron Ltd | 新規ピリミジン誘導体およびその製造法 |
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GB2359078A (en) | 2000-02-11 | 2001-08-15 | Astrazeneca Uk Ltd | Pharmaceutically active pyrimidine derivatives |
ATE255584T1 (de) | 2000-02-11 | 2003-12-15 | Astrazeneca Ab | Pyrimidinverbindungen und ihre verwendung als modulatoren der chemokin-rezeptor-aktivität |
IL152682A0 (en) | 2000-05-31 | 2003-06-24 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
CN1255391C (zh) | 2000-07-07 | 2006-05-10 | 安吉奥金尼药品有限公司 | 作为血管破坏剂的colchinol衍生物 |
PL359181A1 (en) | 2000-07-07 | 2004-08-23 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
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TWI328007B (en) | 2002-01-16 | 2010-08-01 | Astrazeneca Ab | Novel compounds |
GB0217431D0 (en) | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
DE60318219T2 (de) | 2002-08-24 | 2009-01-15 | Astrazeneca Ab | PYRIMIDINDERIVATE ALS MODULATOREN DER AKTIVITuT VON CHEMOKINREZEPTOREN |
EP1809624B1 (en) | 2004-08-28 | 2013-11-20 | AstraZeneca AB | Pyrimidine sulphonamide derivatives as chemokine receptor modulators |
-
2002
- 2002-07-27 GB GBGB0217431.6A patent/GB0217431D0/en not_active Ceased
-
2003
- 2003-07-23 AU AU2003281684A patent/AU2003281684B2/en not_active Ceased
- 2003-07-23 UA UAA200500513A patent/UA80283C2/uk unknown
- 2003-07-23 WO PCT/GB2003/003175 patent/WO2004011443A1/en active Application Filing
- 2003-07-23 KR KR1020057001454A patent/KR101074626B1/ko not_active IP Right Cessation
- 2003-07-23 EP EP03740844A patent/EP1527051B1/en not_active Expired - Lifetime
- 2003-07-23 CA CA2493785A patent/CA2493785C/en not_active Expired - Fee Related
- 2003-07-23 BR BR0312967-5A patent/BR0312967A/pt not_active IP Right Cessation
- 2003-07-23 PL PL03375400A patent/PL375400A1/xx not_active Application Discontinuation
- 2003-07-23 JP JP2004523926A patent/JP4619782B2/ja not_active Expired - Fee Related
- 2003-07-23 CN CNB038221497A patent/CN100345829C/zh not_active Expired - Fee Related
- 2003-07-23 RU RU2005101406/04A patent/RU2342366C2/ru not_active IP Right Cessation
- 2003-07-23 NZ NZ537914A patent/NZ537914A/en not_active IP Right Cessation
- 2003-07-23 KR KR1020117006101A patent/KR20110033313A/ko not_active Application Discontinuation
- 2003-07-23 US US10/522,871 patent/US7582644B2/en not_active Expired - Fee Related
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- 2003-07-23 ES ES03740844T patent/ES2392965T3/es not_active Expired - Lifetime
- 2003-07-25 AR AR20030102688A patent/AR040700A1/es unknown
- 2003-07-25 TW TW092120405A patent/TWI340038B/zh not_active IP Right Cessation
- 2003-07-25 MY MYPI20032818A patent/MY139561A/en unknown
- 2003-07-28 EG EG2003070726A patent/EG25893A/xx active
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2005
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- 2005-01-26 ZA ZA200500791A patent/ZA200500791B/en unknown
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- 2005-02-25 NO NO20051042A patent/NO330531B1/no not_active IP Right Cessation
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2009
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009064938A1 (en) * | 2007-11-16 | 2009-05-22 | Abbott Laboratories | Method of treating arthritis |
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