PL3255043T3 - N-(6-(((2r,3s)-3,4-dihydroksybutan-2-yloksy)-2-(4-fluorobenzylotio)pirymidyn-4-ylo)-3- metyloazetydyno-1-sulfonamid jako modulator receptora chemokin - Google Patents
N-(6-(((2r,3s)-3,4-dihydroksybutan-2-yloksy)-2-(4-fluorobenzylotio)pirymidyn-4-ylo)-3- metyloazetydyno-1-sulfonamid jako modulator receptora chemokinInfo
- Publication number
- PL3255043T3 PL3255043T3 PL16202983T PL16202983T PL3255043T3 PL 3255043 T3 PL3255043 T3 PL 3255043T3 PL 16202983 T PL16202983 T PL 16202983T PL 16202983 T PL16202983 T PL 16202983T PL 3255043 T3 PL3255043 T3 PL 3255043T3
- Authority
- PL
- Poland
- Prior art keywords
- dihydroxybutan
- fluorobenzylthio
- methylazetidine
- yloxy
- pyrimidin
- Prior art date
Links
- 102000009410 Chemokine receptor Human genes 0.000 title 1
- 108050000299 Chemokine receptor Proteins 0.000 title 1
- UCCNQCNIPRKLRP-CJNGLKHVSA-N n-[6-[(2r,3s)-3,4-dihydroxybutan-2-yl]oxy-2-[(4-fluorophenyl)methylsulfanyl]pyrimidin-4-yl]-3-methylazetidine-1-sulfonamide Chemical compound N=1C(SCC=2C=CC(F)=CC=2)=NC(O[C@H](C)[C@@H](O)CO)=CC=1NS(=O)(=O)N1CC(C)C1 UCCNQCNIPRKLRP-CJNGLKHVSA-N 0.000 title 1
- 229940075993 receptor modulator Drugs 0.000 title 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—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
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
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- C07C69/84—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring
- C07C69/92—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring with etherified hydroxyl groups
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- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
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- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
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Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161506737P | 2011-07-12 | 2011-07-12 | |
| PCT/GB2012/051620 WO2013008002A1 (en) | 2011-07-12 | 2012-07-10 | N- (6- ( (2r,3s) -3,4-dihydroxybutan-2-yloxy) -2- (4 - fluorobenzylthio) pyrimidin- 4 - yl) -3- methylazetidine- 1 - sulfonamide as chemokine receptor modulator |
| EP12735323.3A EP2731945A1 (en) | 2011-07-12 | 2012-07-10 | N- (6- ( (2r,3s) -3,4-dihydroxybutan-2-yloxy) -2- (4 - fluorobenzylthio) pyrimidin- 4 - yl) -3- methylazetidine- 1 - sulfonamide as chemokine receptor modulator |
| EP16202983.9A EP3255043B1 (en) | 2011-07-12 | 2012-07-10 | N-(6-((2r,3s)-3,4-dihydroxybutan-2-yloxy)-2-(4-fluorobenzylthio)pyrimidin-4-yl)-3- methylazetidine-1-sulfonamide as chemokine receptor modulator |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL3255043T3 true PL3255043T3 (pl) | 2021-07-12 |
Family
ID=46513787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL16202983T PL3255043T3 (pl) | 2011-07-12 | 2012-07-10 | N-(6-(((2r,3s)-3,4-dihydroksybutan-2-yloksy)-2-(4-fluorobenzylotio)pirymidyn-4-ylo)-3- metyloazetydyno-1-sulfonamid jako modulator receptora chemokin |
Country Status (38)
| Country | Link |
|---|---|
| US (3) | US8735413B2 (pl) |
| EP (2) | EP2731945A1 (pl) |
| JP (2) | JP6006308B2 (pl) |
| KR (1) | KR101946664B1 (pl) |
| CN (1) | CN103781781B (pl) |
| AR (2) | AR087168A1 (pl) |
| AU (2) | AU2012282316B2 (pl) |
| BR (1) | BR112014000636B1 (pl) |
| CA (1) | CA2841859C (pl) |
| CL (1) | CL2014000079A1 (pl) |
| CO (1) | CO6852072A2 (pl) |
| CR (1) | CR20140007A (pl) |
| CU (2) | CU24292B1 (pl) |
| CY (1) | CY1124329T1 (pl) |
| DK (1) | DK3255043T3 (pl) |
| DO (1) | DOP2013000308A (pl) |
| EA (1) | EA027821B1 (pl) |
| EC (1) | ECSP14013130A (pl) |
| ES (1) | ES2861927T3 (pl) |
| HR (1) | HRP20210413T1 (pl) |
| HU (1) | HUE053703T2 (pl) |
| IL (1) | IL230398A (pl) |
| LT (1) | LT3255043T (pl) |
| MX (2) | MX353334B (pl) |
| MY (1) | MY180039A (pl) |
| NI (1) | NI201400002A (pl) |
| PE (2) | PE20141944A1 (pl) |
| PH (1) | PH12014500107A1 (pl) |
| PL (1) | PL3255043T3 (pl) |
| PT (1) | PT3255043T (pl) |
| RS (1) | RS61608B1 (pl) |
| SG (1) | SG10201605619XA (pl) |
| SI (1) | SI3255043T1 (pl) |
| SM (1) | SMT202100173T1 (pl) |
| TW (2) | TWI659026B (pl) |
| UY (1) | UY34191A (pl) |
| WO (1) | WO2013008002A1 (pl) |
| ZA (1) | ZA201401059B (pl) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012007748A1 (en) | 2010-07-13 | 2012-01-19 | Astrazeneca Ab | New crystalline forms of n-[2-[[(2,3-difluoropheny)methyl)thio]-6-{[(1r,2s)-2,3-dihydroxy-1- methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide |
| WO2013008002A1 (en) * | 2011-07-12 | 2013-01-17 | 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 |
| EP3141235A1 (en) * | 2012-12-06 | 2017-03-15 | IP Gesellschaft für Management mbH | N-(6-((2r,3s)-3,4-dihydroxybutan-2-yloxy)-2-(4-fluorobenzylthio)pyrimidin-4-yl)-3-methylazetidine-l -sulfonamide |
| CN109152780B (zh) * | 2016-03-11 | 2021-10-01 | 阿迪亚生命科学公司 | 用于治疗结晶性关节病症的cxcr-2抑制剂 |
| EP3681861A4 (en) * | 2017-09-12 | 2021-06-09 | Ardea Biosciences, Inc. | CXCR-2 INHIBITORS FOR THE TREATMENT OF DISORDERS |
| WO2020249690A1 (en) | 2019-06-12 | 2020-12-17 | Nouryon Chemicals International B.V. | Process for the production of diacyl peroxides |
| ES2963356T3 (es) * | 2019-06-12 | 2024-03-26 | Nouryon Chemicals Int Bv | Método para aislar ácido carboxílico a partir de una corriente lateral acuosa |
| EP3983370B1 (en) | 2019-06-12 | 2023-08-02 | Nouryon Chemicals International B.V. | Process for the production of diacyl peroxides |
| JP7336541B2 (ja) | 2019-06-12 | 2023-08-31 | ヌーリオン ケミカルズ インターナショナル ベスローテン フェノーツハップ | 過酸化ジアシルを生成するためのプロセス |
| US12215074B2 (en) | 2019-06-12 | 2025-02-04 | Nouryon Chemicals International B.V. | Process for the production of peroxyesters |
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|---|---|---|---|---|
| US3457278A (en) * | 1964-10-15 | 1969-07-22 | Geigy Chem Corp | Cyclopropyl-4-sulfanilamido-pyrimidines |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| WO1997030035A1 (en) | 1996-02-13 | 1997-08-21 | Zeneca Limited | Quinazoline derivatives as vegf inhibitors |
| ES2169355T3 (es) | 1996-03-05 | 2002-07-01 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina. |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| FI981521A0 (fi) * | 1998-07-01 | 1998-07-01 | Orion Corp | Substituoidut beta-diketonit ja niiden käyttö |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| IL152682A0 (en) | 2000-05-31 | 2003-06-24 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| BR0112224A (pt) | 2000-07-07 | 2003-06-10 | Angiogene Pharm Ltd | Composto, composição farmacêutica, uso de um composto ou de um sal, solvato ou pró-droga farmaceuticamente aceitável do mesmo, e, processo para preparar um composto |
| HUP0301742A3 (en) | 2000-07-07 | 2005-08-29 | Angiogene Pharm Ltd | Colchinol derivatives as angiogenesis inhibitors, process for producing them, pharmaceutical compositions containing them and their use |
| GB0217431D0 (en) | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
| GB0419235D0 (en) * | 2004-08-28 | 2004-09-29 | Astrazeneca Ab | Compounds |
| AU2005279045B2 (en) | 2004-08-28 | 2009-11-26 | Astrazeneca Ab | Pyrimidine sulphonamide derivatives as chemokine receptor modulators |
| PL1973884T3 (pl) * | 2006-01-19 | 2017-05-31 | Orchid Pharma Limited | Nowe związki heterocykliczne |
| WO2008157273A1 (en) * | 2007-06-14 | 2008-12-24 | Smithkline Beecham Corporation | Chemical compounds |
| CA2730477A1 (en) | 2008-07-16 | 2010-01-21 | Astrazeneca Ab | Pyrimidyl sulfonaminde derivative and its use for the treatment of chemokine mediated diseases |
| CN102105434A (zh) | 2008-07-25 | 2011-06-22 | 巴斯夫欧洲公司 | 3-氨基甲基-1-环己基胺及其生产方法 |
| WO2012007748A1 (en) * | 2010-07-13 | 2012-01-19 | Astrazeneca Ab | New crystalline forms of n-[2-[[(2,3-difluoropheny)methyl)thio]-6-{[(1r,2s)-2,3-dihydroxy-1- methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide |
| WO2013008002A1 (en) * | 2011-07-12 | 2013-01-17 | 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 |
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