AR117002A2 - Proceso para la preparación de inhibidores de quinasa c-fms - Google Patents
Proceso para la preparación de inhibidores de quinasa c-fmsInfo
- Publication number
- AR117002A2 AR117002A2 ARP190103246A ARP190103246A AR117002A2 AR 117002 A2 AR117002 A2 AR 117002A2 AR P190103246 A ARP190103246 A AR P190103246A AR P190103246 A ARP190103246 A AR P190103246A AR 117002 A2 AR117002 A2 AR 117002A2
- Authority
- AR
- Argentina
- Prior art keywords
- preparation
- kinase
- formula
- compound
- fms inhibitors
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 238000002360 preparation method Methods 0.000 title abstract 3
- 101000916644 Homo sapiens Macrophage colony-stimulating factor 1 receptor Proteins 0.000 title 1
- 102100028198 Macrophage colony-stimulating factor 1 receptor Human genes 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 108010058398 Macrophage Colony-Stimulating Factor Receptor Proteins 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 239000005483 tyrosine kinase inhibitor Substances 0.000 abstract 1
Classifications
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- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/30—Oxygen atoms, e.g. delta-lactones
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- 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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- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
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Abstract
La presente se refiere a un proceso para la preparación de intermediarios útiles en la síntesis de inhibidores de proteína tirosina quinasa, más particularmente, inhibidores de quinasa c-fms. Reivindicación 1: Un proceso para la preparación de un compuesto de fórmula (1), estando el proceso caracterizado porque comprende: hacer reaccionar un compuesto de la fórmula (2) con NfsulphF, en presencia de DBU; en un solvente orgánico; a una temperatura de aproximadamente 0ºC a aproximadamente temperatura ambiente; para obtener el compuesto correspondiente de la fórmula (1).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261680446P | 2012-08-07 | 2012-08-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR117002A2 true AR117002A2 (es) | 2021-06-30 |
Family
ID=48980367
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP130102808A AR092070A1 (es) | 2012-08-07 | 2013-08-07 | Proceso para la preparacion de inhibidores de quinasa c-fms |
| ARP190103246A AR117002A2 (es) | 2012-08-07 | 2019-11-06 | Proceso para la preparación de inhibidores de quinasa c-fms |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP130102808A AR092070A1 (es) | 2012-08-07 | 2013-08-07 | Proceso para la preparacion de inhibidores de quinasa c-fms |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US9029352B2 (es) |
| EP (2) | EP2882744B8 (es) |
| JP (1) | JP6290884B2 (es) |
| CN (2) | CN104520295B (es) |
| AR (2) | AR092070A1 (es) |
| AU (2) | AU2013299926B2 (es) |
| ES (2) | ES2607807T3 (es) |
| IN (1) | IN2015DN00660A (es) |
| JO (2) | JO3248B1 (es) |
| TW (2) | TWI608004B (es) |
| UY (1) | UY34972A (es) |
| WO (1) | WO2014025679A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102371784B1 (ko) * | 2014-02-18 | 2022-03-07 | 다이이찌 산쿄 가부시키가이샤 | 활성화 혈액 응고 제 X 인자 (FXa) 의 저해약의 제조 방법 |
| TW201811326A (zh) | 2016-07-18 | 2018-04-01 | 比利時商健生藥品公司 | 4-氰基-n-(2-(4,4-二甲基環己-1-烯-1-基)-6-(2,2,6,6-四甲基四氫-2h-哌喃-4-基)吡啶-3-基)-1h-咪唑-2-甲醯胺之鹽形式 |
| TWI752980B (zh) | 2016-07-18 | 2022-01-21 | 比利時商健生藥品公司 | 4-氰基-n-(2-(4,4-二甲基環己-1-烯-1-基)-6-(2,2,6,6-四甲基四氫-2h-哌喃-4-基)吡啶-3-基)-1h-咪唑-2-甲醯胺之晶型 |
| JP6831558B2 (ja) * | 2016-08-23 | 2021-02-17 | 株式会社Hbcフナト | 脳機能改善組成物 |
| WO2018160917A1 (en) * | 2017-03-03 | 2018-09-07 | Janssen Biotech, Inc. | Co-therapy comprising a small molecule csf-1r inhibitor and an agonistic antibody that specifically binds cd40 for the treatment of cancer |
| WO2020222109A1 (en) | 2019-05-02 | 2020-11-05 | Janssen Biotech, Inc. | Csf-1/csf-1r gene set |
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| US2466420A (en) | 1947-11-26 | 1949-04-05 | Eastman Kodak Co | Ketene condensation products with aldehydes |
| US3226394A (en) | 1964-06-16 | 1965-12-28 | Shulton Inc | Pyridylethylated anthranilamides and derivatives thereof |
| CH504416A (de) | 1966-12-05 | 1971-03-15 | Ciba Geigy Ag | Verfahren zur Herstellung von aromatischen Sulfamoylverbindungen |
| US4551540A (en) | 1983-01-17 | 1985-11-05 | Borg-Warner Chemicals, Inc. | Substituted 2,5-dimethylpyrroles |
| US5190541A (en) | 1990-10-17 | 1993-03-02 | Boston Scientific Corporation | Surgical instrument and method |
| EP1306095A3 (en) | 1992-03-05 | 2003-06-25 | Board Of Regents, The University Of Texas System | Methods and compositions for targeting the vasculature of solid tumors |
| US5474765A (en) | 1992-03-23 | 1995-12-12 | Ut Sw Medical Ctr At Dallas | Preparation and use of steroid-polyanionic polymer-based conjugates targeted to vascular endothelial cells |
| US5686472A (en) | 1992-10-29 | 1997-11-11 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| US5593992A (en) | 1993-07-16 | 1997-01-14 | Smithkline Beecham Corporation | Compounds |
| WO1996011932A1 (en) | 1994-10-14 | 1996-04-25 | Smithkline Beecham Plc | 2-(imidazol-4-yl)carbapeneme derivatives, intermediates thereof and use as antibacterials |
| CA2216943C (en) | 1995-04-19 | 2003-06-17 | Boston Scientific Limited | Drug release coated stent |
| US6117432A (en) | 1995-04-20 | 2000-09-12 | Societe D'exploitation De Produits Pour Les Industries Chimiques (S.E.P.P.I.C.) | Therapeutic composition comprising an antigen or an in vivo generator of a compound comprising an amino acid sequence |
| TW349948B (en) | 1995-10-31 | 1999-01-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 2-quinolone derivatives |
| GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
| DE69635966T2 (de) | 1995-12-08 | 2006-11-30 | Janssen Pharmaceutica N.V. | (Imidazol-5-yl)Methyl-2-Chinolinonderivate als Farnesyl Protein transferase Inhibitoren |
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| US6011029A (en) | 1996-02-26 | 2000-01-04 | Bristol-Myers Squibb Company | Inhibitors of farnesyl protein transferase |
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-
2013
- 2013-08-05 ES ES13748242.8T patent/ES2607807T3/es active Active
- 2013-08-05 JP JP2015526603A patent/JP6290884B2/ja not_active Expired - Fee Related
- 2013-08-05 AU AU2013299926A patent/AU2013299926B2/en not_active Ceased
- 2013-08-05 US US13/959,158 patent/US9029352B2/en active Active
- 2013-08-05 IN IN660DEN2015 patent/IN2015DN00660A/en unknown
- 2013-08-05 ES ES16172842.3T patent/ES2658773T3/es active Active
- 2013-08-05 EP EP13748242.8A patent/EP2882744B8/en not_active Not-in-force
- 2013-08-05 EP EP16172842.3A patent/EP3091006B1/en not_active Not-in-force
- 2013-08-05 CN CN201380041841.0A patent/CN104520295B/zh not_active Expired - Fee Related
- 2013-08-05 WO PCT/US2013/053602 patent/WO2014025679A1/en not_active Ceased
- 2013-08-05 CN CN201710504413.7A patent/CN107266405A/zh active Pending
- 2013-08-06 JO JOP/2013/0237A patent/JO3248B1/ar active
- 2013-08-06 TW TW102128026A patent/TWI608004B/zh not_active IP Right Cessation
- 2013-08-06 TW TW106125831A patent/TWI646090B/zh not_active IP Right Cessation
- 2013-08-07 UY UY0001034972A patent/UY34972A/es unknown
- 2013-08-07 AR ARP130102808A patent/AR092070A1/es active IP Right Grant
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2015
- 2015-05-06 US US14/705,457 patent/US20150232439A1/en not_active Abandoned
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2017
- 2017-03-01 AU AU2017201415A patent/AU2017201415C1/en not_active Ceased
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2018
- 2018-02-15 JO JOP/2018/0012A patent/JOP20180012A1/ar unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| ES2607807T3 (es) | 2017-04-04 |
| TW201408664A (zh) | 2014-03-01 |
| TW201741292A (zh) | 2017-12-01 |
| WO2014025679A1 (en) | 2014-02-13 |
| ES2658773T3 (es) | 2018-03-12 |
| IN2015DN00660A (es) | 2015-06-26 |
| US20150232439A1 (en) | 2015-08-20 |
| JO3248B1 (ar) | 2018-09-16 |
| US9029352B2 (en) | 2015-05-12 |
| JP2015524471A (ja) | 2015-08-24 |
| AU2017201415B2 (en) | 2019-01-03 |
| AU2013299926A1 (en) | 2015-05-21 |
| TWI608004B (zh) | 2017-12-11 |
| EP2882744A1 (en) | 2015-06-17 |
| AR092070A1 (es) | 2015-03-18 |
| UY34972A (es) | 2014-02-28 |
| HK1210616A1 (en) | 2016-04-29 |
| CN104520295B (zh) | 2017-07-18 |
| EP3091006A1 (en) | 2016-11-09 |
| EP3091006B1 (en) | 2018-01-17 |
| JP6290884B2 (ja) | 2018-03-07 |
| AU2013299926B2 (en) | 2017-06-01 |
| HK1209418A1 (en) | 2016-04-01 |
| CN107266405A (zh) | 2017-10-20 |
| US20140045789A1 (en) | 2014-02-13 |
| EP2882744B1 (en) | 2016-09-21 |
| AU2017201415A1 (en) | 2017-03-16 |
| JOP20180012A1 (ar) | 2019-01-30 |
| EP2882744B8 (en) | 2016-11-09 |
| AU2017201415C1 (en) | 2019-05-23 |
| CN104520295A (zh) | 2015-04-15 |
| TWI646090B (zh) | 2019-01-01 |
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