JP5603770B2 - Ccr2受容体拮抗薬およびその使用 - Google Patents
Ccr2受容体拮抗薬およびその使用 Download PDFInfo
- Publication number
- JP5603770B2 JP5603770B2 JP2010509818A JP2010509818A JP5603770B2 JP 5603770 B2 JP5603770 B2 JP 5603770B2 JP 2010509818 A JP2010509818 A JP 2010509818A JP 2010509818 A JP2010509818 A JP 2010509818A JP 5603770 B2 JP5603770 B2 JP 5603770B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- amino
- chloro
- methyl
- quinazoline
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- SPOQOVBTEXXRSU-UHFFFAOYSA-N CC(C(c(cc1)cc(Cl)c1Cl)=NN1)=CC1=O Chemical compound CC(C(c(cc1)cc(Cl)c1Cl)=NN1)=CC1=O SPOQOVBTEXXRSU-UHFFFAOYSA-N 0.000 description 1
- NRUHHOVQAIAJLM-UHFFFAOYSA-N CC(C)(C)OC(N1CCN(CC2OCCN(Cc3ccccc3)C2)CC1)=O Chemical compound CC(C)(C)OC(N1CCN(CC2OCCN(Cc3ccccc3)C2)CC1)=O NRUHHOVQAIAJLM-UHFFFAOYSA-N 0.000 description 1
- NAVSGTUNFADZMR-UHFFFAOYSA-N CC(C)N1CC(C(N(CC2)CCN2c2n[nH]c(-c3cc(C=C)cc(Cl)c3)c2)=O)NCC1 Chemical compound CC(C)N1CC(C(N(CC2)CCN2c2n[nH]c(-c3cc(C=C)cc(Cl)c3)c2)=O)NCC1 NAVSGTUNFADZMR-UHFFFAOYSA-N 0.000 description 1
- VTHZDAFPOSMJMY-UHFFFAOYSA-N CC(C)N1CC(C(N(CC2)CCN2c2n[nH]c(-c3cc(Cl)cc(Cl)c3)c2)=O)OCC1 Chemical compound CC(C)N1CC(C(N(CC2)CCN2c2n[nH]c(-c3cc(Cl)cc(Cl)c3)c2)=O)OCC1 VTHZDAFPOSMJMY-UHFFFAOYSA-N 0.000 description 1
- NQXZAUNUYSPZCA-XRWIVYGQSA-N CC(CCC1)CN1[C@H](CC1)CC[C@]1(c(cc1)cnc1OC)O Chemical compound CC(CCC1)CN1[C@H](CC1)CC[C@]1(c(cc1)cnc1OC)O NQXZAUNUYSPZCA-XRWIVYGQSA-N 0.000 description 1
- PHNFCQMBGZQDLX-UHFFFAOYSA-N CC1CN(CC(CC2)CCC2(c(cc2)cnc2OC)O)CCC1 Chemical compound CC1CN(CC(CC2)CCC2(c(cc2)cnc2OC)O)CCC1 PHNFCQMBGZQDLX-UHFFFAOYSA-N 0.000 description 1
- ZVAZLNQNANWZDB-UHFFFAOYSA-N CC1CN(Cc2ccc(cc[nH]3)c3c2)CCC1 Chemical compound CC1CN(Cc2ccc(cc[nH]3)c3c2)CCC1 ZVAZLNQNANWZDB-UHFFFAOYSA-N 0.000 description 1
- 0 CCc1ccc(C*2CCCCC2)cc1 Chemical compound CCc1ccc(C*2CCCCC2)cc1 0.000 description 1
- TZIMSHYSZIQBMK-UHFFFAOYSA-N CN(C)CCNC(CC1)CCN1c1ccc(-c(cc2Cl)ccc2Cl)nn1 Chemical compound CN(C)CCNC(CC1)CCN1c1ccc(-c(cc2Cl)ccc2Cl)nn1 TZIMSHYSZIQBMK-UHFFFAOYSA-N 0.000 description 1
- XHDCUCTVUKCSPL-UHFFFAOYSA-N CSC(SC)=CC(c(cc1Cl)ccc1Cl)=O Chemical compound CSC(SC)=CC(c(cc1Cl)ccc1Cl)=O XHDCUCTVUKCSPL-UHFFFAOYSA-N 0.000 description 1
- UGXNHQRUQGXTQA-UHFFFAOYSA-N Clc(cc1)c(C2CC2)cc1-c1cc(N2CCN(CC(C3)OCCN3C3CCCCC3)CC2)n[nH]1 Chemical compound Clc(cc1)c(C2CC2)cc1-c1cc(N2CCN(CC(C3)OCCN3C3CCCCC3)CC2)n[nH]1 UGXNHQRUQGXTQA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07109376.9 | 2007-05-31 | ||
| EP07109376 | 2007-05-31 | ||
| PCT/EP2008/056573 WO2008145681A2 (en) | 2007-05-31 | 2008-05-29 | Ccr2 receptor antagonists and uses thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010528089A JP2010528089A (ja) | 2010-08-19 |
| JP2010528089A5 JP2010528089A5 (enExample) | 2011-07-14 |
| JP5603770B2 true JP5603770B2 (ja) | 2014-10-08 |
Family
ID=38752546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010509818A Active JP5603770B2 (ja) | 2007-05-31 | 2008-05-29 | Ccr2受容体拮抗薬およびその使用 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8653262B2 (enExample) |
| EP (1) | EP2155689B1 (enExample) |
| JP (1) | JP5603770B2 (enExample) |
| AR (1) | AR066799A1 (enExample) |
| CA (1) | CA2687931C (enExample) |
| CL (1) | CL2008001593A1 (enExample) |
| TW (1) | TW200904434A (enExample) |
| WO (1) | WO2008145681A2 (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS55634B1 (sr) | 2005-12-13 | 2017-06-30 | Incyte Holdings Corp | Heteroaril substituisani pirolo[2,3-b]piridini i pirolo[2,3-b]pirimidini kao inhibitori janus kinaze |
| DE102006039003A1 (de) | 2006-08-19 | 2008-02-21 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Verbindungen |
| JP5603770B2 (ja) | 2007-05-31 | 2014-10-08 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ccr2受容体拮抗薬およびその使用 |
| HUE043732T2 (hu) | 2007-06-13 | 2019-09-30 | Incyte Holdings Corp | Januskináz gátló hatású (R)-3-(4-(7H pirrolo[2,3-d]pirimidin-4-il)-1H-pirazol-1-il)-3-ciklopentilpropánnitril sók alkalmazása |
| JP5250627B2 (ja) | 2007-08-14 | 2013-07-31 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規化合物 |
| EP2025675A1 (de) | 2007-08-14 | 2009-02-18 | Boehringer Ingelheim International GmbH | Arylsulfonamide mit analgetischer Wirkung |
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| KR20120030447A (ko) | 2009-05-22 | 2012-03-28 | 인사이트 코포레이션 | Jak 저해물질로서 3-[4-(7h-피롤로[2,3-d]피리미딘-4-일)-1h-피라졸-1-일]옥탄- 또는 헵탄-니트릴 |
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| US8946218B2 (en) | 2010-05-12 | 2015-02-03 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| US8877745B2 (en) | 2010-05-12 | 2014-11-04 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
| WO2011144501A1 (en) | 2010-05-17 | 2011-11-24 | Boehringer Ingelheim International Gmbh | Ccr2 antagonists and uses thereof |
| US20110288107A1 (en) | 2010-05-21 | 2011-11-24 | Bhavnish Parikh | Topical formulation for a jak inhibitor |
| JP5636094B2 (ja) * | 2010-05-25 | 2014-12-03 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ccr2受容体アンタゴニスト |
| JP5721242B2 (ja) | 2010-06-01 | 2015-05-20 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規ccr2アンタゴニスト |
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| EP2640725B1 (en) | 2010-11-19 | 2015-01-07 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors |
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| AU2012253237B2 (en) * | 2011-05-12 | 2015-09-24 | Bionomics Limited | Methods for preparing naphthyridines |
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| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
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| WO2014169087A2 (en) * | 2013-04-10 | 2014-10-16 | The Trustees Of Columbia University In The City Of New York | Treatment of proximal spinal muscular atrophy |
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| WO2015184305A1 (en) | 2014-05-30 | 2015-12-03 | Incyte Corporation | TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 |
| WO2016128343A1 (en) * | 2015-02-09 | 2016-08-18 | F. Hoffmann-La Roche Ag | Compounds for the treatment of cancer |
| EP3053577A1 (en) * | 2015-02-09 | 2016-08-10 | F. Hoffmann-La Roche AG | Compounds for the treatment of cancer |
| EP3317270B1 (en) | 2015-07-02 | 2020-05-13 | Centrexion Therapeutics Corporation | (4-((3r,4r)-3-methoxytetrahydro-pyran-4-ylamino)piperidin-1-yl)(5-methyl-6-(((2r,6s)-6-(p-tolyl)tetrahydro-2h-pyran-2-yl)methylamino)pyrimidin-4yl)methanone citrate |
| CN112480079B (zh) * | 2017-11-08 | 2022-03-11 | 北京嘉林药业股份有限公司 | 化合物及其治疗癌症的用途 |
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- 2008-05-29 JP JP2010509818A patent/JP5603770B2/ja active Active
- 2008-05-29 EP EP08760165.4A patent/EP2155689B1/en active Active
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| CA2687931A1 (en) | 2008-12-04 |
| AR066799A1 (es) | 2009-09-16 |
| WO2008145681A2 (en) | 2008-12-04 |
| EP2155689B1 (en) | 2015-07-08 |
| CA2687931C (en) | 2016-05-24 |
| WO2008145681A3 (en) | 2009-03-05 |
| US20100204209A1 (en) | 2010-08-12 |
| US8653262B2 (en) | 2014-02-18 |
| TW200904434A (en) | 2009-02-01 |
| CL2008001593A1 (es) | 2009-09-11 |
| EP2155689A2 (en) | 2010-02-24 |
| JP2010528089A (ja) | 2010-08-19 |
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