JP2011512412A5 - - Google Patents
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- Publication number
- JP2011512412A5 JP2011512412A5 JP2010547712A JP2010547712A JP2011512412A5 JP 2011512412 A5 JP2011512412 A5 JP 2011512412A5 JP 2010547712 A JP2010547712 A JP 2010547712A JP 2010547712 A JP2010547712 A JP 2010547712A JP 2011512412 A5 JP2011512412 A5 JP 2011512412A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- lower alkyl
- optionally substituted
- independently
- pharmaceutically acceptable
- 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.)
- Pending
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- 150000001875 compounds Chemical class 0.000 claims 19
- 125000000217 alkyl group Chemical group 0.000 claims 12
- 125000001475 halogen functional group Chemical group 0.000 claims 5
- 150000001204 N-oxides Chemical class 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 239000000651 prodrug Substances 0.000 claims 4
- 229940002612 prodrugs Drugs 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000011780 sodium chloride Substances 0.000 claims 4
- 239000012453 solvate Substances 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- -1 benzenesulfonamide compound Chemical class 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N Azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims 1
- NVBFHJWHLNUMCV-UHFFFAOYSA-N Sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 claims 1
- 230000000996 additive Effects 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 102000009410 chemokine receptors Human genes 0.000 claims 1
- 108050000299 chemokine receptors Proteins 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 230000001404 mediated Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000003431 oxalo group Chemical group 0.000 claims 1
- 230000001575 pathological Effects 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- ZBHAIZGVCIXSFF-UHFFFAOYSA-N CC(C1)C(S(NCCc(ccc(Cl)c2)c2Cl)(=O)=O)=CC(NC(c2cccc(Cl)c2)=O)=C1N1CCN(CCCN(C)C)CC1 Chemical compound CC(C1)C(S(NCCc(ccc(Cl)c2)c2Cl)(=O)=O)=CC(NC(c2cccc(Cl)c2)=O)=C1N1CCN(CCCN(C)C)CC1 ZBHAIZGVCIXSFF-UHFFFAOYSA-N 0.000 description 1
- IPYGCIBQODYDDJ-UHFFFAOYSA-N CN(C)CCC(N(CC1)CCN1c(ccc(C(CCCCc(ccc(Cl)c1)c1Cl)=O)c1)c1NC(c1cc(C(O)=O)ccc1)=O)=O Chemical compound CN(C)CCC(N(CC1)CCN1c(ccc(C(CCCCc(ccc(Cl)c1)c1Cl)=O)c1)c1NC(c1cc(C(O)=O)ccc1)=O)=O IPYGCIBQODYDDJ-UHFFFAOYSA-N 0.000 description 1
- UNMYDMGJCLVXRL-UHFFFAOYSA-N CN(C)CCC(N(CC1)CCN1c(ccc(C(NCCc(ccc(Cl)c1)c1Cl)=O)c1)c1NC(c1cc(Cl)ccc1)=O)=O Chemical compound CN(C)CCC(N(CC1)CCN1c(ccc(C(NCCc(ccc(Cl)c1)c1Cl)=O)c1)c1NC(c1cc(Cl)ccc1)=O)=O UNMYDMGJCLVXRL-UHFFFAOYSA-N 0.000 description 1
- GFXRDOFRFRNQSK-UHFFFAOYSA-N CNCCC(N(CC1)CCN1c(ccc(C(NCCc(ccc(Cl)c1)c1Cl)=O)c1)c1NC(c1cc(Cl)ccc1)=O)=O Chemical compound CNCCC(N(CC1)CCN1c(ccc(C(NCCc(ccc(Cl)c1)c1Cl)=O)c1)c1NC(c1cc(Cl)ccc1)=O)=O GFXRDOFRFRNQSK-UHFFFAOYSA-N 0.000 description 1
- VBLNVRLKHKXYSN-UHFFFAOYSA-O C[NH+](C)CCN(CC1)CCN1c(ccc(C(NCCc(c(Cl)c1)ccc1Cl)=O)c1)c1NC(c(cc1C2)ccc1NC2=O)=O Chemical compound C[NH+](C)CCN(CC1)CCN1c(ccc(C(NCCc(c(Cl)c1)ccc1Cl)=O)c1)c1NC(c(cc1C2)ccc1NC2=O)=O VBLNVRLKHKXYSN-UHFFFAOYSA-O 0.000 description 1
- HGILWWCUMUZSIH-UHFFFAOYSA-N O=C(CCN1CC1)N(CC1)CCN1c(ccc(C(NCCc(c(Cl)c1)ccc1Cl)=O)c1)c1NC(c1cccc(Cl)c1)=O Chemical compound O=C(CCN1CC1)N(CC1)CCN1c(ccc(C(NCCc(c(Cl)c1)ccc1Cl)=O)c1)c1NC(c1cccc(Cl)c1)=O HGILWWCUMUZSIH-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2973808P | 2008-02-19 | 2008-02-19 | |
| PCT/US2009/034340 WO2009105435A1 (en) | 2008-02-19 | 2009-02-18 | Inhibitors of the chemokine receptor cxcr3 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011512412A JP2011512412A (ja) | 2011-04-21 |
| JP2011512412A5 true JP2011512412A5 (US07794700-20100914-C00152.png) | 2012-03-22 |
Family
ID=40527535
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010547712A Pending JP2011512412A (ja) | 2008-02-19 | 2009-02-18 | ケモカイン受容体ＣｘＣＲ３の阻害剤 |
Country Status (25)
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20091576A1 (es) | 2008-02-19 | 2009-11-05 | Sanofi Aventis | DERIVADOS DE 3-(AMIDO O SULFAMIDO)-4-(4-AZINIL SUSTITUIDO)BENZAMIDA COMO INHIBIDORES DEL RECEPTOR DE QUIMIOQUINAS CxCR3 |
| EP2424840B1 (en) | 2009-04-27 | 2014-08-06 | Boehringer Ingelheim International GmbH | Cxcr3 receptor antagonists |
| WO2011084985A1 (en) * | 2010-01-07 | 2011-07-14 | Boehringer Ingelheim International Gmbh | Cxcr3 receptor antagonists |
| KR101251788B1 (ko) | 2010-12-06 | 2013-04-08 | 기아자동차주식회사 | 차량 연비 정보 단말표시 시스템 및 그 방법 |
| ES2649995T3 (es) | 2011-07-18 | 2018-01-16 | Merck Patent Gmbh | Benzamidas |
| EP2601950A1 (en) | 2011-12-06 | 2013-06-12 | Sanofi | Cycloalkane carboxylic acid derivatives as CXCR3 receptor antagonists |
| AU2013208082B2 (en) | 2012-01-10 | 2017-07-20 | Merck Patent Gmbh | Benzamide derivatives as modulators of the follicle stimulating hormone |
| CA2861020C (en) | 2012-02-02 | 2018-07-17 | Actelion Pharmaceuticals Ltd | 4-(benzoimidazol-2-yl)-thiazole compounds and related aza derivatives and their use as cxcr3 receptor modulators |
| EP2666769A1 (en) | 2012-05-23 | 2013-11-27 | Sanofi | Substituted B-amino acid derivatives as CXCR3 receptor antagonist |
| ES2671323T3 (es) | 2013-07-22 | 2018-06-06 | Idorsia Pharmaceuticals Ltd | Derivados 1¿(piperazin¿1¿il)¿2¿([1,2,4]triazol¿1¿il)¿etanona |
| AR099789A1 (es) | 2014-03-24 | 2016-08-17 | Actelion Pharmaceuticals Ltd | Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina |
| JP2017538659A (ja) * | 2014-09-10 | 2017-12-28 | エピザイム インコーポレイテッド | Ｓｍｙｄ阻害剤 |
| PL3245203T3 (pl) | 2015-01-15 | 2019-05-31 | Idorsia Pharmaceuticals Ltd | Pochodne hydroksyalkilopiperazyny jako modulatory receptora cxcr3 |
| AR103399A1 (es) | 2015-01-15 | 2017-05-10 | Actelion Pharmaceuticals Ltd | Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3 |
| WO2018183145A1 (en) * | 2017-03-26 | 2018-10-04 | Takeda Pharmaceutical Company Limited | Piperidinyl- and piperazinyl-substituted heteroaromatic carboxamides as modulators of gpr6 |
| CN116410159B (zh) * | 2023-06-09 | 2023-08-22 | 济南国鼎医药科技有限公司 | 一种恩曲替尼中间体的制备方法及其应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2052541A5 (US07794700-20100914-C00152.png) | 1969-06-13 | 1971-04-09 | Takeda Chemical Industries Ltd | |
| US3840556A (en) | 1971-05-28 | 1974-10-08 | Lilly Co Eli | Penicillin conversion by halogen electrophiles and anti-bacterials derived thereby |
| US6124319A (en) | 1997-01-21 | 2000-09-26 | Merck & Co., Inc. | 3,3-disubstituted piperidines as modulators of chemokine receptor activity |
| US6469002B1 (en) | 2001-04-19 | 2002-10-22 | Millennium Pharmaceuticals, Inc. | Imidazolidine compounds |
| US6794379B2 (en) | 2001-06-06 | 2004-09-21 | Tularik Inc. | CXCR3 antagonists |
| GB0203994D0 (en) | 2002-02-20 | 2002-04-03 | Celltech R&D Ltd | Chemical compounds |
| EP1554253A4 (en) | 2002-06-03 | 2006-09-20 | Smithkline Beecham Corp | IMIDAZOLIUM COMPOUNDS INHIBITORS OF CXCR3 |
| US6734659B1 (en) | 2002-06-13 | 2004-05-11 | Mykrolis Corporation | Electronic interface for use with dual electrode capacitance diaphragm gauges |
| US7776862B2 (en) * | 2005-02-16 | 2010-08-17 | Schering Corporation | Pyridyl and phenyl substituted piperazine-piperidines with CXCR3 antagonist activity |
| KR20070107060A (ko) | 2005-02-16 | 2007-11-06 | 쉐링 코포레이션 | Ｃｘｃｒ3 길항제 활성을 갖는 피라지닐 치환된피페라진-피페리딘 |
| KR20070107075A (ko) * | 2005-02-16 | 2007-11-06 | 쉐링 코포레이션 | Ｃｘｃｒ３ 길항제 활성을 갖는 신규의 헤테로사이클릭치환된 피리딘 또는 페닐 화합물 |
| WO2007002742A1 (en) * | 2005-06-28 | 2007-01-04 | Pharmacopeia, Inc. | Substituted [1,4]-diazepanes as cxcr3 antagonists and their use in the treatment of inflammatory disorders |
| JP2009511582A (ja) | 2005-10-11 | 2009-03-19 | シェーリング コーポレイション | Ｃｘｃｒ３拮抗薬活性を有する置換複素環式化合物 |
| EP1957076A2 (en) | 2005-11-29 | 2008-08-20 | Merck & Co., Inc. | Thiazole derivatives as cxcr3 receptor modulators |
| KR20080106970A (ko) | 2006-03-21 | 2008-12-09 | 쉐링 코포레이션 | Ｃｘｃｒ３ 길항제 활성을 갖는 헤테로사이클릭 치환된 피리딘 화합물 |
| KR20090043512A (ko) | 2006-07-14 | 2009-05-06 | 쉐링 코포레이션 | Ｃｘｃｒ3 길항제 활성을 갖는 헤테로사이클릭 치환된 피페라진 화합물 |
| PE20091576A1 (es) | 2008-02-19 | 2009-11-05 | Sanofi Aventis | DERIVADOS DE 3-(AMIDO O SULFAMIDO)-4-(4-AZINIL SUSTITUIDO)BENZAMIDA COMO INHIBIDORES DEL RECEPTOR DE QUIMIOQUINAS CxCR3 |
-
2009
- 2009-02-17 PE PE2009000232A patent/PE20091576A1/es not_active Application Discontinuation
- 2009-02-18 KR KR1020107018467A patent/KR20100123835A/ko not_active Application Discontinuation
- 2009-02-18 CA CA2715557A patent/CA2715557A1/en not_active Abandoned
- 2009-02-18 WO PCT/US2009/034340 patent/WO2009105435A1/en active Application Filing
- 2009-02-18 AR ARP090100561A patent/AR070430A1/es not_active Application Discontinuation
- 2009-02-18 AU AU2009215643A patent/AU2009215643A1/en not_active Abandoned
- 2009-02-18 BR BRPI0908815A patent/BRPI0908815A2/pt not_active IP Right Cessation
- 2009-02-18 CL CL2009000368A patent/CL2009000368A1/es unknown
- 2009-02-18 CN CN2009801138321A patent/CN102007108A/zh active Pending
- 2009-02-18 EP EP09711984.6A patent/EP2262784B1/en active Active
- 2009-02-18 JP JP2010547712A patent/JP2011512412A/ja active Pending
- 2009-02-18 RU RU2010138577/04A patent/RU2010138577A/ru not_active Application Discontinuation
- 2009-02-18 NZ NZ587380A patent/NZ587380A/en not_active IP Right Cessation
- 2009-02-18 MX MX2010008397A patent/MX2010008397A/es not_active Application Discontinuation
- 2009-02-19 TW TW098105199A patent/TW200948791A/zh unknown
-
2010
- 2010-07-26 ZA ZA2010/05314A patent/ZA201005314B/en unknown
- 2010-07-28 CR CR11604A patent/CR11604A/es not_active Application Discontinuation
- 2010-07-29 NI NI201000132A patent/NI201000132A/es unknown
- 2010-08-06 US US12/852,076 patent/US8268828B2/en active Active
- 2010-08-12 IL IL207597A patent/IL207597A0/en unknown
- 2010-08-18 EC EC2010010409A patent/ECSP10010409A/es unknown
- 2010-08-18 SV SV2010003648A patent/SV2010003648A/es not_active Application Discontinuation
- 2010-08-18 DO DO2010000254A patent/DOP2010000254A/es unknown
- 2010-08-19 CO CO10102315A patent/CO6241113A2/es not_active Application Discontinuation
- 2010-09-13 MA MA33173A patent/MA32191B1/fr unknown
