CL2014000079A1 - El compuesto n-(6-((2r,3s)-3,4-dihidroxibutan-2iloxi)-2-(4-fluorobenciltio) pirimidin-4-ilo)-3-metilacetidina-1-sulfonamida, receptor de qumiocina; forma cristalina; proceso de preparación; compuesto intermediario; composicion farmaceutica; y su uso en asma, rinitis alergica, epoc, sindrome de colon irritable, enfermedad intestinal inflamatoria, entre otras - Google Patents
El compuesto n-(6-((2r,3s)-3,4-dihidroxibutan-2iloxi)-2-(4-fluorobenciltio) pirimidin-4-ilo)-3-metilacetidina-1-sulfonamida, receptor de qumiocina; forma cristalina; proceso de preparación; compuesto intermediario; composicion farmaceutica; y su uso en asma, rinitis alergica, epoc, sindrome de colon irritable, enfermedad intestinal inflamatoria, entre otrasInfo
- Publication number
- CL2014000079A1 CL2014000079A1 CL2014000079A CL2014000079A CL2014000079A1 CL 2014000079 A1 CL2014000079 A1 CL 2014000079A1 CL 2014000079 A CL2014000079 A CL 2014000079A CL 2014000079 A CL2014000079 A CL 2014000079A CL 2014000079 A1 CL2014000079 A1 CL 2014000079A1
- Authority
- CL
- Chile
- Prior art keywords
- compound
- methylacetyidine
- fluorobenzylthio
- epoc
- dihydroxybutane
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 2
- -1 6 - ((2r, 3s) -3,4-dihydroxybutane-2-yloxy) -2- (4-fluorobenzylthio) pyrimidin-4-yl Chemical group 0.000 title 1
- 102000009410 Chemokine receptor Human genes 0.000 title 1
- 108050000299 Chemokine receptor Proteins 0.000 title 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 title 1
- 206010039085 Rhinitis allergic Diseases 0.000 title 1
- 201000010105 allergic rhinitis Diseases 0.000 title 1
- 208000006673 asthma Diseases 0.000 title 1
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 title 1
- 208000002551 irritable bowel syndrome Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- 229940124530 sulfonamide Drugs 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- 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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- C07D239/00—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
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- C07D239/46—Two or more oxygen, sulphur or nitrogen 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
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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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- C07D317/26—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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- C07C69/78—Benzoic acid esters
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- 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
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- Engineering & Computer Science (AREA)
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- Rheumatology (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Immunology (AREA)
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- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Otolaryngology (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161506737P | 2011-07-12 | 2011-07-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2014000079A1 true CL2014000079A1 (es) | 2014-06-27 |
Family
ID=46513787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2014000079A CL2014000079A1 (es) | 2011-07-12 | 2014-01-10 | El compuesto n-(6-((2r,3s)-3,4-dihidroxibutan-2iloxi)-2-(4-fluorobenciltio) pirimidin-4-ilo)-3-metilacetidina-1-sulfonamida, receptor de qumiocina; forma cristalina; proceso de preparación; compuesto intermediario; composicion farmaceutica; y su uso en asma, rinitis alergica, epoc, sindrome de colon irritable, enfermedad intestinal inflamatoria, entre otras |
Country Status (38)
| Country | Link |
|---|---|
| US (3) | US8735413B2 (es) |
| EP (2) | EP2731945A1 (es) |
| JP (2) | JP6006308B2 (es) |
| KR (1) | KR101946664B1 (es) |
| CN (1) | CN103781781B (es) |
| AR (2) | AR087168A1 (es) |
| AU (2) | AU2012282316B2 (es) |
| BR (1) | BR112014000636B1 (es) |
| CA (1) | CA2841859C (es) |
| CL (1) | CL2014000079A1 (es) |
| CO (1) | CO6852072A2 (es) |
| CR (1) | CR20140007A (es) |
| CU (2) | CU24292B1 (es) |
| CY (1) | CY1124329T1 (es) |
| DK (1) | DK3255043T3 (es) |
| DO (1) | DOP2013000308A (es) |
| EA (1) | EA027821B1 (es) |
| EC (1) | ECSP14013130A (es) |
| ES (1) | ES2861927T3 (es) |
| HR (1) | HRP20210413T1 (es) |
| HU (1) | HUE053703T2 (es) |
| IL (1) | IL230398A (es) |
| LT (1) | LT3255043T (es) |
| MX (2) | MX342874B (es) |
| MY (1) | MY180039A (es) |
| NI (1) | NI201400002A (es) |
| PE (2) | PE20181069A1 (es) |
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| PL (1) | PL3255043T3 (es) |
| PT (1) | PT3255043T (es) |
| RS (1) | RS61608B1 (es) |
| SG (1) | SG10201605619XA (es) |
| SI (1) | SI3255043T1 (es) |
| SM (1) | SMT202100173T1 (es) |
| TW (2) | TWI633098B (es) |
| UY (1) | UY34191A (es) |
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| ZA (1) | ZA201401059B (es) |
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 |
| 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. |
| 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 |
| EP3426253A4 (en) * | 2016-03-11 | 2019-11-06 | Ardea Biosciences, Inc. | CXCR-2 INHIBITORS FOR THE TREATMENT OF CRYSTALARTHROPATHIES |
| WO2019055509A1 (en) * | 2017-09-12 | 2019-03-21 | Ardea Biosciences, Inc. | INHIBITORS OF CXCR-2 FOR THE TREATMENT OF DISORDERS |
| ES2961184T3 (es) | 2019-06-12 | 2024-03-08 | Nouryon Chemicals Int Bv | Proceso para la producción de peróxidos de diacilo |
| ES2963357T3 (es) | 2019-06-12 | 2024-03-26 | Nouryon Chemicals Int Bv | Proceso para la producción de peróxidos de diacilo |
| WO2020249689A1 (en) | 2019-06-12 | 2020-12-17 | Nouryon Chemicals International B.V. | Process for the production of peroxyesters |
| US20220306490A1 (en) * | 2019-06-12 | 2022-09-29 | Nouryon Chemicals International B.V. | Method for isolating carboxylic acid from an aqueous side stream |
| ES2963382T3 (es) | 2019-06-12 | 2024-03-26 | Nouryon Chemicals Int Bv | Proceso para la producción de peróxidos de diacilo |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
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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 |
| JP4471404B2 (ja) | 1996-02-13 | 2010-06-02 | アストラゼネカ ユーケイ リミテッド | Vegfインヒビターとしてのキナゾリン誘導体 |
| ATE211134T1 (de) | 1996-03-05 | 2002-01-15 | 4-anilinochinazolin derivate | |
| 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 |
| NZ522074A (en) | 2000-05-31 | 2004-06-25 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| JP2004502766A (ja) | 2000-07-07 | 2004-01-29 | アンギオジェン・ファーマシューティカルズ・リミテッド | 血管損傷剤としてのコルヒノール誘導体 |
| CA2410562A1 (en) | 2000-07-07 | 2002-01-31 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
| GB0217431D0 (en) | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
| RU2408587C2 (ru) | 2004-08-24 | 2011-01-10 | Астразенека Аб | Производные пиримидинсульфонамида в качестве модуляторов рецепторов хемокинов |
| GB0419235D0 (en) * | 2004-08-28 | 2004-09-29 | Astrazeneca Ab | Compounds |
| JP5237115B2 (ja) * | 2006-01-19 | 2013-07-17 | オーキッド リサーチ ラボラトリーズ リミテッド | 新規複素環類 |
| WO2008157273A1 (en) * | 2007-06-14 | 2008-12-24 | Smithkline Beecham Corporation | Chemical compounds |
| KR20110031462A (ko) * | 2008-07-16 | 2011-03-28 | 아스트라제네카 아베 | 피리미딜 술폰아미드 유도체 및 케모카인 매개 질환의 치료를 위한 그의 용도 |
| 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 |
| 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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