EA201490077A1 - N-(6-((2r,3s)-3,4-дигидроксибутан-2-илокси)-2-(4-фторбензилтио)пиримидин-4-ил)-3-метилазетидин-1-сульфонамид в качестве модуляторов рецептора хемокина - Google Patents
N-(6-((2r,3s)-3,4-дигидроксибутан-2-илокси)-2-(4-фторбензилтио)пиримидин-4-ил)-3-метилазетидин-1-сульфонамид в качестве модуляторов рецептора хемокинаInfo
- Publication number
- EA201490077A1 EA201490077A1 EA201490077A EA201490077A EA201490077A1 EA 201490077 A1 EA201490077 A1 EA 201490077A1 EA 201490077 A EA201490077 A EA 201490077A EA 201490077 A EA201490077 A EA 201490077A EA 201490077 A1 EA201490077 A1 EA 201490077A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compound
- pyrymidin
- fluorbenzyltiho
- iloxi
- dihydroxybutan
- Prior art date
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- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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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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- 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
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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
- C07D317/26—Radicals substituted by doubly bound oxygen or sulfur atoms or by two such atoms singly bound to the same carbon atom
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- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/78—Benzoic acid esters
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- 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
- C07D307/12—Radicals substituted by oxygen atoms
Abstract
Предложено соединение, представляющее собой (а) пиримидинсульфонамид формулы (I) или (б) его фармацевтически приемлемую соль, кристаллические формы данного соединения, способы получения данного соединения, фармацевтические промежуточные соединения, используемые в получении данного соединения, и фармацевтические композиции, содержащие данное соединение. Указанное соединение полезно в лечении заболевания/состояния, при котором полезно модулирование активности рецептора хемокинов.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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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 |
Publications (2)
Publication Number | Publication Date |
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EA201490077A1 true EA201490077A1 (ru) | 2014-10-30 |
EA027821B1 EA027821B1 (ru) | 2017-09-29 |
Family
ID=46513787
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201490077A EA027821B1 (ru) | 2011-07-12 | 2012-07-10 | N-(6-((2r,3s)-3,4-дигидроксибутан-2-илокси)-2-(4-фторбензилтио)пиримидин-4-ил)-3-метилазетидин-1-сульфонамид в качестве модулятора рецептора хемокина |
Country Status (37)
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US (3) | US8735413B2 (ru) |
EP (2) | EP3255043B1 (ru) |
JP (2) | JP6006308B2 (ru) |
KR (1) | KR101946664B1 (ru) |
CN (1) | CN103781781B (ru) |
AR (2) | AR087168A1 (ru) |
AU (2) | AU2012282316B2 (ru) |
BR (1) | BR112014000636B1 (ru) |
CA (1) | CA2841859C (ru) |
CL (1) | CL2014000079A1 (ru) |
CO (1) | CO6852072A2 (ru) |
CR (1) | CR20140007A (ru) |
CU (2) | CU24292B1 (ru) |
CY (1) | CY1124329T1 (ru) |
DK (1) | DK3255043T3 (ru) |
DO (1) | DOP2013000308A (ru) |
EA (1) | EA027821B1 (ru) |
EC (1) | ECSP14013130A (ru) |
ES (1) | ES2861927T3 (ru) |
HK (1) | HK1245779A1 (ru) |
HR (1) | HRP20210413T1 (ru) |
HU (1) | HUE053703T2 (ru) |
IL (1) | IL230398A (ru) |
LT (1) | LT3255043T (ru) |
MX (2) | MX342874B (ru) |
MY (1) | MY180039A (ru) |
NI (1) | NI201400002A (ru) |
PE (2) | PE20181069A1 (ru) |
PL (1) | PL3255043T3 (ru) |
PT (1) | PT3255043T (ru) |
RS (1) | RS61608B1 (ru) |
SG (1) | SG10201605619XA (ru) |
SI (1) | SI3255043T1 (ru) |
TW (2) | TWI659026B (ru) |
UY (1) | UY34191A (ru) |
WO (1) | WO2013008002A1 (ru) |
ZA (1) | ZA201401059B (ru) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2593448A1 (en) | 2010-07-13 | 2013-05-22 | AstraZeneca AB | New cristalline forms of n-[2-[[(2,3-difluoropheny)methyl)thio]-6-{[(1r,2s)-2,3- dihydroxy-1-methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide |
MX342874B (es) * | 2011-07-12 | 2016-10-17 | Astrazeneca Ab | N-(6-((2r,3s)-3,4-dihidroxibutan-2-iloxi)-2-(4-fluorobenciltio)pi rimidin-4-il)-3-metilacetidina-1-sulfonamida como modulador del receptor de quimiocina. |
EP2740458B1 (en) * | 2012-12-06 | 2016-08-03 | IP Gesellschaft für Management mbH | Packaging comprising forms of sodium salt of 4-tert-butyl-N-[4-chloro-2-(1-oxy-pyridine-4-carbonyl)-phenyl]-benzenesulfonamide |
BR112018068393A2 (pt) * | 2016-03-11 | 2019-01-15 | Ardea Biosciences Inc | inibidores de cxcr-2 para o tratamento de distúrbios de artropatia por cristais |
EP3681861A4 (en) * | 2017-09-12 | 2021-06-09 | Ardea Biosciences, Inc. | CXCR-2 INHIBITORS FOR THE TREATMENT OF DISORDERS |
JP7355858B2 (ja) * | 2019-06-12 | 2023-10-03 | 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 | 水性側流からカルボン酸を単離するための方法 |
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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 |
HUP9901155A3 (en) | 1996-02-13 | 2003-04-28 | Astrazeneca Ab | Quinazoline derivatives as vegf inhibitors |
KR100489174B1 (ko) | 1996-03-05 | 2005-09-30 | 제네카-파마 소시에떼아노님 | 4-아닐리노퀴나졸린유도체 |
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 |
CA2406979A1 (en) | 2000-05-31 | 2001-12-06 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
EE200300015A (et) | 2000-07-07 | 2004-10-15 | Angiogene Pharmaceuticals Limited | Kolhinooli derivaadid kui angiogeneesi inhibiitorid |
IL153484A0 (en) | 2000-07-07 | 2003-07-06 | Angiogene Pharm Ltd | Colchinol derivatives as angiogenesis inhibitors |
GB0217431D0 (en) | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
GB0419235D0 (en) * | 2004-08-28 | 2004-09-29 | Astrazeneca Ab | Compounds |
EP2311827A1 (en) * | 2004-08-28 | 2011-04-20 | AstraZeneca AB | Thiopyrimidine derivative, useful as an intermediate for chemokine receptor modulators. |
CA2637631C (en) * | 2006-01-19 | 2014-04-29 | Orchid Research Laboratories Limited | Pyrimidine compounds and uses thereof |
WO2008157273A1 (en) * | 2007-06-14 | 2008-12-24 | Smithkline Beecham Corporation | Chemical compounds |
CN102159555A (zh) * | 2008-07-16 | 2011-08-17 | 阿斯利康(瑞典)有限公司 | 嘧啶基氨磺酰衍生物及其治疗趋化因子介导的疾病的用途 |
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 |
EP2593448A1 (en) * | 2010-07-13 | 2013-05-22 | AstraZeneca AB | New cristalline forms of n-[2-[[(2,3-difluoropheny)methyl)thio]-6-{[(1r,2s)-2,3- dihydroxy-1-methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide |
MX342874B (es) * | 2011-07-12 | 2016-10-17 | Astrazeneca Ab | N-(6-((2r,3s)-3,4-dihidroxibutan-2-iloxi)-2-(4-fluorobenciltio)pi rimidin-4-il)-3-metilacetidina-1-sulfonamida como modulador del receptor de quimiocina. |
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2012
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