JP2011527667A5 - - Google Patents
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- Publication number
- JP2011527667A5 JP2011527667A5 JP2011513994A JP2011513994A JP2011527667A5 JP 2011527667 A5 JP2011527667 A5 JP 2011527667A5 JP 2011513994 A JP2011513994 A JP 2011513994A JP 2011513994 A JP2011513994 A JP 2011513994A JP 2011527667 A5 JP2011527667 A5 JP 2011527667A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- tetrahydro
- methoxy
- pyrimido
- ylamino
- 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
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- -1 phenyl cyclopropyl Chemical group 0.000 claims 4
- 150000002431 hydrogen Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- XJDFPABNFMGUQZ-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-phenylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2CCC1=CC=CC=C1 XJDFPABNFMGUQZ-UHFFFAOYSA-N 0.000 claims 1
- TUQMYIJNTSGUGF-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-phenylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(oxan-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCOCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2CCC1=CC=CC=C1 TUQMYIJNTSGUGF-UHFFFAOYSA-N 0.000 claims 1
- PSUBGYPXALNCMG-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-phenylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-methylbenzamide Chemical compound COC1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3C=CC=CC=3)C2=N1 PSUBGYPXALNCMG-UHFFFAOYSA-N 0.000 claims 1
- XSDGPZQANIZACZ-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-phenylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(N)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3C=CC=CC=3)C2=N1 XSDGPZQANIZACZ-UHFFFAOYSA-N 0.000 claims 1
- PCPAXXKTKQUPHR-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-phenylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3C=CC=CC=3)C2=N1 PCPAXXKTKQUPHR-UHFFFAOYSA-N 0.000 claims 1
- NGAFYUZTCNBCGI-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-phenylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-n-[3-(dimethylamino)propyl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCCN(C)C)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3C=CC=CC=3)C2=N1 NGAFYUZTCNBCGI-UHFFFAOYSA-N 0.000 claims 1
- KVBACVCSBJSAER-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-thiophen-2-ylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2CCC1=CC=CS1 KVBACVCSBJSAER-UHFFFAOYSA-N 0.000 claims 1
- DGGHCJPFKMNPAU-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-thiophen-2-ylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(oxan-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCOCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2CCC1=CC=CS1 DGGHCJPFKMNPAU-UHFFFAOYSA-N 0.000 claims 1
- JSFTXPUPTJTYTB-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-thiophen-2-ylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-methylbenzamide Chemical compound COC1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3SC=CC=3)C2=N1 JSFTXPUPTJTYTB-UHFFFAOYSA-N 0.000 claims 1
- KMWJCCMWYIKRNP-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-thiophen-2-ylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(N)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3SC=CC=3)C2=N1 KMWJCCMWYIKRNP-UHFFFAOYSA-N 0.000 claims 1
- MNHDFLRMCRZSOS-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(2-thiophen-2-ylethyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-n-[3-(dimethylamino)propyl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCCN(C)C)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCC=3SC=CC=3)C2=N1 MNHDFLRMCRZSOS-UHFFFAOYSA-N 0.000 claims 1
- QIMBUKMFWMBEHR-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(3-phenylpropyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2CCCC1=CC=CC=C1 QIMBUKMFWMBEHR-UHFFFAOYSA-N 0.000 claims 1
- PHXLWWFFQDNSSE-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(3-phenylpropyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(oxan-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCOCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2CCCC1=CC=CC=C1 PHXLWWFFQDNSSE-UHFFFAOYSA-N 0.000 claims 1
- DMMUXYAYHYDDLV-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(3-phenylpropyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-methylbenzamide Chemical compound COC1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCCC=3C=CC=CC=3)C2=N1 DMMUXYAYHYDDLV-UHFFFAOYSA-N 0.000 claims 1
- UXZZINQYOKUPEO-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(3-phenylpropyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(N)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCCC=3C=CC=CC=3)C2=N1 UXZZINQYOKUPEO-UHFFFAOYSA-N 0.000 claims 1
- XXIJBRADQSRHDK-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(3-phenylpropyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCCC=3C=CC=CC=3)C2=N1 XXIJBRADQSRHDK-UHFFFAOYSA-N 0.000 claims 1
- GHTYTXXJOCCCQB-UHFFFAOYSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-(3-phenylpropyl)-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-n-[3-(dimethylamino)propyl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCCN(C)C)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2CCCC=3C=CC=CC=3)C2=N1 GHTYTXXJOCCCQB-UHFFFAOYSA-N 0.000 claims 1
- QREWJFAVPDUZPY-LADGPHEKSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-[(1r,2s)-2-phenylcyclopropyl]-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C1([C@@H]2C[C@H]2N2CC(F)(F)C(=O)N(C)C3=CN=C(N=C32)NC2=CC=C(C=C2OC)C(=O)NC2CCN(C)CC2)=CC=CC=C1 QREWJFAVPDUZPY-LADGPHEKSA-N 0.000 claims 1
- AVYWETQIOGLARX-FUHWJXTLSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-[(1r,2s)-2-phenylcyclopropyl]-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(N)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2[C@H]3[C@@H](C3)C=3C=CC=CC=3)C2=N1 AVYWETQIOGLARX-FUHWJXTLSA-N 0.000 claims 1
- IXGLPNQCLBXUHO-FUHWJXTLSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-[(1r,2s)-2-phenylcyclopropyl]-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2[C@H]3[C@@H](C3)C=3C=CC=CC=3)C2=N1 IXGLPNQCLBXUHO-FUHWJXTLSA-N 0.000 claims 1
- IWZPVFATWJHPPC-JTHBVZDNSA-N 4-[[7,7-difluoro-5-methyl-6-oxo-9-[(1r,2s)-2-phenylcyclopropyl]-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-n-[3-(dimethylamino)propyl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCCN(C)C)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2[C@H]3[C@@H](C3)C=3C=CC=CC=3)C2=N1 IWZPVFATWJHPPC-JTHBVZDNSA-N 0.000 claims 1
- GLTMSDBAMFENHK-UHFFFAOYSA-N 4-[[7,7-difluoro-9-[(4-methoxyphenyl)methyl]-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C1=CC(OC)=CC=C1CN1C2=NC(NC=3C(=CC(=CC=3)C(=O)NC3CCN(C)CC3)OC)=NC=C2N(C)C(=O)C(F)(F)C1 GLTMSDBAMFENHK-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7338808P | 2008-06-18 | 2008-06-18 | |
| US61/073,388 | 2008-06-18 | ||
| PCT/EP2009/057144 WO2009153197A1 (en) | 2008-06-18 | 2009-06-10 | Halo-substituted pyrimidodiazepines as plkl inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011527667A JP2011527667A (ja) | 2011-11-04 |
| JP2011527667A5 true JP2011527667A5 (enExample) | 2012-08-02 |
Family
ID=41431858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011513994A Abandoned JP2011527667A (ja) | 2008-06-18 | 2009-06-10 | ハロ置換ピリミドジアゼピン |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8003785B2 (enExample) |
| EP (1) | EP2303889A1 (enExample) |
| JP (1) | JP2011527667A (enExample) |
| WO (1) | WO2009153197A1 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ584760A (en) * | 2007-09-25 | 2012-03-30 | Takeda Pharmaceutical | Polo-like kinase inhibitors |
| EP2361242B1 (en) | 2008-10-17 | 2018-08-01 | Oryzon Genomics, S.A. | Oxidase inhibitors and their use |
| WO2010084160A1 (en) | 2009-01-21 | 2010-07-29 | Oryzon Genomics S.A. | Phenylcyclopropylamine derivatives and their medical use |
| AU2010299579A1 (en) * | 2009-09-25 | 2012-05-03 | Vertex Pharmaceuticals Incorporated | Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors |
| NZ599342A (en) | 2009-09-25 | 2014-04-30 | Vertex Pharma | Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors |
| KR101736218B1 (ko) | 2009-09-25 | 2017-05-16 | 오리존 지노믹스 에스.에이. | 라이신 특이적 디메틸라아제-1 억제제 및 이의 용도 |
| EP2486002B1 (en) | 2009-10-09 | 2019-03-27 | Oryzon Genomics, S.A. | Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use |
| JP5504898B2 (ja) * | 2010-01-08 | 2014-05-28 | セントラル硝子株式会社 | ジフルオロシクロプロパン化合物の製造方法 |
| WO2011106574A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Inhibitors for antiviral use |
| US9186337B2 (en) | 2010-02-24 | 2015-11-17 | Oryzon Genomics S.A. | Lysine demethylase inhibitors for diseases and disorders associated with Hepadnaviridae |
| ES2607081T3 (es) | 2010-04-19 | 2017-03-29 | Oryzon Genomics, S.A. | Inhibidores de desmetilasa específica de lisina-1 y su uso |
| US9006449B2 (en) | 2010-07-29 | 2015-04-14 | Oryzon Genomics, S.A. | Cyclopropylamine derivatives useful as LSD1 inhibitors |
| LT2598482T (lt) | 2010-07-29 | 2018-07-10 | Oryzon Genomics, S.A. | Demetilazės lsd1 inhibitoriai arilciklopropilamino pagrindu ir jų medicininis panaudojimas |
| US9061966B2 (en) | 2010-10-08 | 2015-06-23 | Oryzon Genomics S.A. | Cyclopropylamine inhibitors of oxidases |
| WO2012072713A2 (en) | 2010-11-30 | 2012-06-07 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae |
| WO2012107498A1 (en) | 2011-02-08 | 2012-08-16 | Oryzon Genomics S.A. | Lysine demethylase inhibitors for myeloproliferative disorders |
| SI2776394T1 (sl) | 2011-10-20 | 2019-05-31 | Oryzon Genomics, S.A. | Spojine (hetero)aril ciklopropilamina kot inhibitorji LSD1 |
| EP3736265A1 (en) | 2011-10-20 | 2020-11-11 | Oryzon Genomics, S.A. | (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors |
| CA2873097A1 (en) | 2012-05-11 | 2013-11-14 | Todd M. Hansen | Pyridazine and pyridine derivatives as nampt inhibitors |
| CA2918910A1 (en) | 2013-07-25 | 2015-01-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of transcription factors and uses thereof |
| JP2017504651A (ja) | 2014-01-31 | 2017-02-09 | ダナ−ファーバー キャンサー インスティテュート， インコーポレイテッド | ジアゼパン誘導体の使用 |
| KR20160115953A (ko) | 2014-01-31 | 2016-10-06 | 다나-파버 캔서 인스티튜트 인크. | 디아미노피리미딘 벤젠술폰 유도체 및 그의 용도 |
| JP2017526741A (ja) | 2014-08-08 | 2017-09-14 | ダナ−ファーバー キャンサー インスティテュート， インコーポレイテッド | ジアゼパン誘導体およびその使用 |
| CN105646398B (zh) * | 2014-12-05 | 2018-09-07 | 上海医药工业研究院 | N-((1r,4r)-4-(4-(环丙基甲基)哌嗪-1-基)环己基)乙酰胺的制备方法 |
| WO2016201370A1 (en) | 2015-06-12 | 2016-12-15 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| PE20181287A1 (es) | 2015-09-11 | 2018-08-07 | Dana Farber Cancer Inst Inc | Ciano tienotriazolpirazinas y usos de las mismas |
| HK1256419A1 (zh) | 2015-09-11 | 2019-09-20 | 达纳-法伯癌症研究所股份有限公司 | 乙酰胺噻吩並三唑並二氮雜環庚三烯及其用途 |
| SG10201913450PA (en) | 2015-11-25 | 2020-03-30 | Dana Farber Cancer Inst Inc | Bivalent bromodomain inhibitors and uses thereof |
| US20230158158A1 (en) * | 2020-03-27 | 2023-05-25 | Uppthera | Pyrazolo quinazoline derivative compounds inducing selective degradation of plk1 |
| WO2022145989A1 (ko) * | 2020-12-31 | 2022-07-07 | (주) 업테라 | 선택적 plk1 억제제로서의 피리미도디아제핀 유도체 |
| CA3228601A1 (en) * | 2021-08-10 | 2023-02-16 | Soo Hee RYU | Novel plk1 degradation inducing compound |
| GB202313514D0 (en) | 2023-09-05 | 2023-10-18 | Cambridge Entpr Ltd | Treatment of inflammatory diseases |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU7491400A (en) | 1999-09-17 | 2001-04-17 | Abbott Gmbh & Co. Kg | Kinase inhibitors as therapeutic agents |
| NZ531928A (en) | 2001-09-04 | 2005-10-28 | Boehringer Ingelheim Pharma | Novel dihydropteridinones, method for producing the same and the use thereof as medicaments |
| US6806272B2 (en) * | 2001-09-04 | 2004-10-19 | Boehringer Ingelheim Pharma Kg | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions |
| KR20080095902A (ko) | 2006-02-14 | 2008-10-29 | 버텍스 파마슈티칼스 인코포레이티드 | 단백질 키나제의 억제제로서 유용한 디하이드로디아제핀 |
| TW200808325A (en) * | 2006-07-06 | 2008-02-16 | Astrazeneca Ab | Novel compounds |
| PT2139892E (pt) * | 2007-03-22 | 2011-11-21 | Takeda Pharmaceutical | Pirimidodiazepinas substituídas úteis como inibidores da plk1 |
| NZ584760A (en) * | 2007-09-25 | 2012-03-30 | Takeda Pharmaceutical | Polo-like kinase inhibitors |
-
2009
- 2009-06-10 EP EP09765777A patent/EP2303889A1/en not_active Withdrawn
- 2009-06-10 JP JP2011513994A patent/JP2011527667A/ja not_active Abandoned
- 2009-06-10 WO PCT/EP2009/057144 patent/WO2009153197A1/en not_active Ceased
- 2009-06-16 US US12/485,108 patent/US8003785B2/en not_active Expired - Fee Related