JP2011503006A5 - - Google Patents
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- Publication number
- JP2011503006A5 JP2011503006A5 JP2010532330A JP2010532330A JP2011503006A5 JP 2011503006 A5 JP2011503006 A5 JP 2011503006A5 JP 2010532330 A JP2010532330 A JP 2010532330A JP 2010532330 A JP2010532330 A JP 2010532330A JP 2011503006 A5 JP2011503006 A5 JP 2011503006A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- haloalkyl
- independently
- 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.)
- Abandoned
Links
- -1 cyano, hydroxy, amino Chemical group 0.000 claims description 54
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 24
- 229910052736 halogen Inorganic materials 0.000 claims description 20
- 150000002367 halogens Chemical class 0.000 claims description 20
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 18
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 12
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 10
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 claims description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 8
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 8
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 7
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 6
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims description 6
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 6
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 6
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 6
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 6
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 6
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 6
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 6
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims description 6
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims description 6
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 6
- 201000010099 disease Diseases 0.000 claims description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims description 6
- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 6
- 125000001624 naphthyl group Chemical group 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 230000000844 anti-bacterial effect Effects 0.000 claims description 5
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 4
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 4
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 4
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 4
- 125000006815 (C4-C10) cycloalkylaminocarbonyl group Chemical group 0.000 claims description 4
- 125000006781 (C4-C10) cycloalkylcarbonyl group Chemical group 0.000 claims description 4
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 4
- 125000004858 cycloalkoxyalkyl group Chemical group 0.000 claims description 3
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims description 2
- 125000006798 (C1-C6) haloalkylamino group Chemical group 0.000 claims description 2
- 125000006765 (C2-C6) haloalkenyloxy group Chemical group 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
- 241000235349 Ascomycota Species 0.000 claims description 2
- 241000221198 Basidiomycota Species 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims description 2
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims description 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims description 2
- 230000000855 fungicidal effect Effects 0.000 claims description 2
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 claims description 2
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 244000000003 plant pathogen Species 0.000 claims 1
- 238000011156 evaluation Methods 0.000 description 2
- FWDWWURUAKTWRY-UHFFFAOYSA-N 4-[2-(2-chloro-6-methylanilino)pyridin-4-yl]-n-(oxan-4-yl)pyrimidin-2-amine Chemical compound CC1=CC=CC(Cl)=C1NC1=CC(C=2N=C(NC3CCOCC3)N=CC=2)=CC=N1 FWDWWURUAKTWRY-UHFFFAOYSA-N 0.000 description 1
- XNNGIBBOOHUDLN-UHFFFAOYSA-N 4-[2-(3-chloroanilino)pyridin-4-yl]-n-(1-methoxypropan-2-yl)pyrimidin-2-amine Chemical compound COCC(C)NC1=NC=CC(C=2C=C(NC=3C=C(Cl)C=CC=3)N=CC=2)=N1 XNNGIBBOOHUDLN-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- RFFJJTULQODEAZ-JTQLQIEISA-N n-(3,5-difluorophenyl)-4-[2-[[(2s)-1-methoxypropan-2-yl]amino]pyrimidin-4-yl]-1,3,5-triazin-2-amine Chemical compound COC[C@H](C)NC1=NC=CC(C=2N=C(NC=3C=C(F)C=C(F)C=3)N=CN=2)=N1 RFFJJTULQODEAZ-JTQLQIEISA-N 0.000 description 1
- CGRFEOXSDORMQK-UHFFFAOYSA-N n-(3-fluorophenyl)-4-[2-(1-methoxypropan-2-ylamino)pyrimidin-4-yl]-1,3,5-triazin-2-amine Chemical compound COCC(C)NC1=NC=CC(C=2N=C(NC=3C=C(F)C=CC=3)N=CN=2)=N1 CGRFEOXSDORMQK-UHFFFAOYSA-N 0.000 description 1
- CGRFEOXSDORMQK-NSHDSACASA-N n-(3-fluorophenyl)-4-[2-[[(2s)-1-methoxypropan-2-yl]amino]pyrimidin-4-yl]-1,3,5-triazin-2-amine Chemical compound COC[C@H](C)NC1=NC=CC(C=2N=C(NC=3C=C(F)C=CC=3)N=CN=2)=N1 CGRFEOXSDORMQK-NSHDSACASA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US212907P | 2007-11-06 | 2007-11-06 | |
| PCT/US2008/082398 WO2009061761A2 (en) | 2007-11-06 | 2008-11-05 | Fungicidal heterocyclic amines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011503006A JP2011503006A (ja) | 2011-01-27 |
| JP2011503006A5 true JP2011503006A5 (enExample) | 2011-12-22 |
Family
ID=40521581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010532330A Abandoned JP2011503006A (ja) | 2007-11-06 | 2008-11-05 | 殺菌性複素環アミン |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US8026359B2 (enExample) |
| EP (1) | EP2205086B1 (enExample) |
| JP (1) | JP2011503006A (enExample) |
| KR (1) | KR20100088150A (enExample) |
| CN (1) | CN101902912A (enExample) |
| AU (1) | AU2008324833A1 (enExample) |
| BR (1) | BRPI0817135A2 (enExample) |
| MX (1) | MX2010005033A (enExample) |
| WO (1) | WO2009061761A2 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012101065A2 (en) * | 2011-01-28 | 2012-08-02 | Novartis Ag | Pyrimidine biaryl amine compounds and their uses |
| US9133187B2 (en) | 2011-02-28 | 2015-09-15 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
| ES2552989T3 (es) | 2011-08-04 | 2015-12-03 | Array Biopharma, Inc. | Compuestos de quinazolina como inhibidores de la cinasa de serina / treonina |
| PE20150666A1 (es) | 2012-03-01 | 2015-05-06 | Array Biopharma Inc | Inhibidores de serina/treonina cinasa |
| SG11201406584TA (en) | 2012-04-24 | 2014-11-27 | Vertex Pharma | Dna-pk inhibitors |
| CA2882750A1 (en) | 2012-08-27 | 2014-03-06 | Jim Blake | Serine/threonine kinase inhibitors for the treatment of hyperproliferative|diseases |
| RS62649B1 (sr) | 2013-03-12 | 2021-12-31 | Vertex Pharma | Inhibitori dnk-pk |
| KR102411227B1 (ko) | 2013-10-17 | 2022-06-21 | 버텍스 파마슈티칼스 인코포레이티드 | Dna-pk 억제제로서 (s)-n-메틸-8-(1-((2'-메틸-[4,5'-비피리미딘]-6-일)아미노)프로판-2-일)퀴놀린-4-카복스아미드 및 이의 듀테로화된 유도체의 공결정 |
| JP6589241B2 (ja) * | 2013-12-18 | 2019-10-16 | 出光興産株式会社 | 化合物、有機エレクトロルミネッセンス素子用材料、インク組成物、有機エレクトロルミネッセンス素子、電子機器、及び化合物の製造方法 |
| CN106659721B (zh) * | 2014-04-09 | 2021-01-01 | 基因泰克公司 | 用于制备药物的方法 |
| MX394860B (es) | 2016-09-27 | 2025-03-24 | Vertex Pharma | Metodo para tratar cancer usando una combinacion de agentes que dañan adn e inhibidores de proteina cinasa dependiente de adn (adn-pk). |
| EP4178955A1 (en) | 2020-07-11 | 2023-05-17 | Pfizer Inc. | Antiviral heteroaryl ketone derivatives |
| US11351149B2 (en) | 2020-09-03 | 2022-06-07 | Pfizer Inc. | Nitrile-containing antiviral compounds |
| CN119841771B (zh) * | 2025-01-08 | 2026-02-13 | 华中农业大学 | 一种猪链球菌丝氨酸蛋白激酶抑制剂的筛选方法及其应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MXPA02003436A (es) * | 1999-10-07 | 2002-08-20 | Amgen Inc | Inhibidores de triazina cinasa. |
| GB0014022D0 (en) * | 2000-06-08 | 2000-08-02 | Novartis Ag | Organic compounds |
| ATE497603T1 (de) * | 2001-03-02 | 2011-02-15 | Gpc Biotech Ag | Drei-hybrid-assaysystem |
| IL161662A0 (en) * | 2001-11-01 | 2004-09-27 | Janssen Pharmaceutica Nv | Heteroaryl amines as glycogen synthase kinase 3 beta inhibitors (gsk3 inhibitors) |
| GB0307268D0 (en) * | 2003-03-28 | 2003-05-07 | Syngenta Ltd | Organic compounds |
| US20050014753A1 (en) * | 2003-04-04 | 2005-01-20 | Irm Llc | Novel compounds and compositions as protein kinase inhibitors |
| CN1798734A (zh) * | 2003-04-04 | 2006-07-05 | Irm责任有限公司 | 作为蛋白激酶抑制剂的新化合物和组合物 |
| US20050130968A1 (en) * | 2003-10-03 | 2005-06-16 | Irvine Nicholas M. | Fungicidal 4-(2-aminopyridin-4-yl)-N-phenyl-1,3,5-triazin-2-amine derivatives |
| HN2005000795A (es) * | 2004-10-15 | 2010-08-19 | Aventis Pharma Inc | Pirimidinas como antagonistas del receptor de prostaglandina d2 |
| CN101679376A (zh) * | 2007-06-08 | 2010-03-24 | 拜尔农科股份有限公司 | 杀真菌剂杂环-嘧啶基-氨基衍生物 |
-
2008
- 2008-11-05 MX MX2010005033A patent/MX2010005033A/es unknown
- 2008-11-05 CN CN2008801217475A patent/CN101902912A/zh active Pending
- 2008-11-05 KR KR1020107012295A patent/KR20100088150A/ko not_active Withdrawn
- 2008-11-05 AU AU2008324833A patent/AU2008324833A1/en not_active Abandoned
- 2008-11-05 WO PCT/US2008/082398 patent/WO2009061761A2/en not_active Ceased
- 2008-11-05 EP EP08847187.5A patent/EP2205086B1/en not_active Not-in-force
- 2008-11-05 BR BRPI0817135-1A2A patent/BRPI0817135A2/pt not_active Application Discontinuation
- 2008-11-05 JP JP2010532330A patent/JP2011503006A/ja not_active Abandoned
-
2009
- 2009-05-14 US US12/741,047 patent/US8026359B2/en not_active Expired - Fee Related
-
2011
- 2011-08-16 US US13/210,427 patent/US20110301123A1/en not_active Abandoned