JP2006515604A5 - - Google Patents
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- Publication number
- JP2006515604A5 JP2006515604A5 JP2006500010A JP2006500010A JP2006515604A5 JP 2006515604 A5 JP2006515604 A5 JP 2006515604A5 JP 2006500010 A JP2006500010 A JP 2006500010A JP 2006500010 A JP2006500010 A JP 2006500010A JP 2006515604 A5 JP2006515604 A5 JP 2006515604A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrimidine
- methyl
- carbonitrile
- thieno
- methylthieno
- 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
Links
- -1 4- (Diethylamino) -5-methyl-2- (4-nitrophenyl) thieno [2,3-d] pyrimidine-6-carbonitrile 2- (4-chlorophenyl) -4- (diethylamino) -5-methylthieno [ 2,3-d] pyrimidine-6-carbonitrile Chemical compound 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- ZAQMRTFLKPRAPX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-4-[2-hydroxyethyl(methyl)amino]-5-methylthieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound C1=C(OC)C(OC)=CC=C1C1=NC(N(C)CCO)=C(C(C)=C(S2)C#N)C2=N1 ZAQMRTFLKPRAPX-UHFFFAOYSA-N 0.000 description 1
- BSMFHDOOMKDRBW-UHFFFAOYSA-N 4-(diethylamino)-2-(3,4-dimethoxyphenyl)-5-methylthieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound N=1C=2SC(C#N)=C(C)C=2C(N(CC)CC)=NC=1C1=CC=C(OC)C(OC)=C1 BSMFHDOOMKDRBW-UHFFFAOYSA-N 0.000 description 1
- AWXXKHKQDQFYMW-UHFFFAOYSA-N 4-(diethylamino)-5-methyl-2-[4-(trifluoromethyl)phenyl]thieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound N=1C=2SC(C#N)=C(C)C=2C(N(CC)CC)=NC=1C1=CC=C(C(F)(F)F)C=C1 AWXXKHKQDQFYMW-UHFFFAOYSA-N 0.000 description 1
- MYJKZQFEQHKVMG-UHFFFAOYSA-N 4-[2-hydroxyethyl(methyl)amino]-2-(4-methoxyphenyl)-5-methylthieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound C1=CC(OC)=CC=C1C1=NC(N(C)CCO)=C(C(C)=C(S2)C#N)C2=N1 MYJKZQFEQHKVMG-UHFFFAOYSA-N 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- VCZNNAKNUVJVGX-UHFFFAOYSA-N 4-methylbenzonitrile Chemical compound CC1=CC=C(C#N)C=C1 VCZNNAKNUVJVGX-UHFFFAOYSA-N 0.000 description 1
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 1
- YSSCHKVBFGJWPV-UHFFFAOYSA-N 5-methyl-2-(4-methylphenyl)-4-oxo-3h-thieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound N1C(=O)C=2C(C)=C(C#N)SC=2N=C1C1=CC=C(C)C=C1 YSSCHKVBFGJWPV-UHFFFAOYSA-N 0.000 description 1
- YXTLFUJDTXUANL-UHFFFAOYSA-N 5-methyl-4-(4-methylpiperazin-1-yl)-2-[4-(trifluoromethyl)phenyl]thieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound C1CN(C)CCN1C1=NC(C=2C=CC(=CC=2)C(F)(F)F)=NC2=C1C(C)=C(C#N)S2 YXTLFUJDTXUANL-UHFFFAOYSA-N 0.000 description 1
- KNVYMJFTTNGDHD-UHFFFAOYSA-N CC1=C(SC=2N=C(N=C(C21)N2CCOCC2)C2=CC=C(C=C2)C)C#N.COC=2C=C(C=CC2OC)C=2N=C(C1=C(N2)SC(=C1C)C#N)N1CCOCC1 Chemical compound CC1=C(SC=2N=C(N=C(C21)N2CCOCC2)C2=CC=C(C=C2)C)C#N.COC=2C=C(C=CC2OC)C=2N=C(C1=C(N2)SC(=C1C)C#N)N1CCOCC1 KNVYMJFTTNGDHD-UHFFFAOYSA-N 0.000 description 1
- IULCNODUMUBMEY-UHFFFAOYSA-N COC1=CC=C(C=C1)C=1N=C(C2=C(N1)SC(=C2C)C#N)N(CC#C)C.ClC2=CC=C(C=C2)C=2N=C(C1=C(N2)SC(=C1C)C#N)N1CCOCC1 Chemical compound COC1=CC=C(C=C1)C=1N=C(C2=C(N1)SC(=C2C)C#N)N(CC#C)C.ClC2=CC=C(C=C2)C=2N=C(C1=C(N2)SC(=C1C)C#N)N1CCOCC1 IULCNODUMUBMEY-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- CTHOBBRGWQVVGK-UHFFFAOYSA-N ethyl 2-amino-5-cyano-4-methylthiophene-3-carboxylate Chemical compound CCOC(=O)C1=C(N)SC(C#N)=C1C CTHOBBRGWQVVGK-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- ZIEWSZYVEDTXGH-UHFFFAOYSA-N pyrimidine-4-carbonitrile Chemical compound N#CC1=CC=NC=N1 ZIEWSZYVEDTXGH-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES200300172A ES2217956B1 (es) | 2003-01-23 | 2003-01-23 | Nuevos derivados de 4-aminotieno(2,3-d)pirimidin-6-carbonitrilo. |
| PCT/EP2004/000584 WO2004065391A1 (en) | 2003-01-23 | 2004-01-23 | 4-AMINOTHIENO[2,3-d]PYRIMIDINE-6-CARBONITRILE DERIVATIVES AS PDE7 INHIBITORS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006515604A JP2006515604A (ja) | 2006-06-01 |
| JP2006515604A5 true JP2006515604A5 (cg-RX-API-DMAC7.html) | 2007-01-25 |
Family
ID=32749101
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006500010A Pending JP2006515604A (ja) | 2003-01-23 | 2004-01-23 | Ｐｄｅ７阻害剤としての４−アミノチエノ［２，３−ｄ］ピリミジン−６−カルボニトリル誘導体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7662814B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1590352B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2006515604A (cg-RX-API-DMAC7.html) |
| CN (1) | CN100582112C (cg-RX-API-DMAC7.html) |
| AT (1) | ATE365742T1 (cg-RX-API-DMAC7.html) |
| DE (1) | DE602004007239T2 (cg-RX-API-DMAC7.html) |
| ES (2) | ES2217956B1 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2004065391A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4895806B2 (ja) * | 2003-04-09 | 2012-03-14 | エクセリクシス， インク． | Ｔｉｅ−２モジュレータと使用方法 |
| US20060014165A1 (en) * | 2003-07-14 | 2006-01-19 | Decode Genetics Ehf. | Methods of diagnosis and treatment for asthma and other respiratory diseases based on haplotype association |
| JP4862654B2 (ja) * | 2004-10-08 | 2012-01-25 | アステラス製薬株式会社 | 芳香環縮合ピリミジン誘導体 |
| TW200621257A (en) * | 2004-10-20 | 2006-07-01 | Astellas Pharma Inc | Pyrimidine derivative fused with nonaromatic ring |
| GB0423653D0 (en) | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| WO2007117995A2 (en) * | 2006-03-30 | 2007-10-18 | Takeda San Diego, Inc. | Kinase inhibitors |
| CL2007001167A1 (es) | 2006-04-26 | 2008-01-25 | Genentech Inc | Compuestos derivados de pirimidina condensada, inhibidores de p13-quinasa; procesos para preparar los compuestos; composicion farmaceutica que los comprende; uso de los compuestos en la preparacion de medicamentos; proceso para preparar la composicion farmaceutica; y kit que incluye a la composicionfarmaceutica. |
| EP2046799B1 (en) * | 2006-04-26 | 2017-07-19 | Genentech, Inc. | Phosphoinositide 3-kinase inhibitor compounds and pharmaceutical compositions containing them |
| NZ572812A (en) | 2006-04-26 | 2010-09-30 | Hoffmann La Roche | THIENO [3, 2-D] PYRIMIDINE Indazole DERIVATIVE USEFUL AS PI3K INHIBITOR |
| GB0608820D0 (en) * | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
| KR20090021218A (ko) | 2006-06-12 | 2009-02-27 | 버텍스 파마슈티칼스 인코포레이티드 | 이온 채널의 조절제로서 유용한 티에노피리미딘 |
| WO2008073785A2 (en) * | 2006-12-07 | 2008-06-19 | Genentech, Inc. | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| JP5284977B2 (ja) * | 2006-12-07 | 2013-09-11 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ホスホイノシチド３−キナーゼ阻害剤化合物及び使用方法 |
| EP2139475B1 (en) * | 2007-03-27 | 2014-12-17 | Omeros Corporation | PDE7 inhibitors for use in the treatment of movement disorders |
| US8637528B2 (en) | 2007-03-27 | 2014-01-28 | Omeros Corporation | Use of PDE7 inhibitors for the treatment of movement disorders |
| PE20090678A1 (es) * | 2007-09-12 | 2009-06-27 | Genentech Inc | Combinaciones de compuestos inhibidores de fosfoinositida 3-quinasa y agentes quimioterapeuticos y los metodos de uso |
| EP2207781B1 (en) * | 2007-09-24 | 2012-11-28 | Genentech, Inc. | Thiazolopyrimidine p13k inhibitor compounds and methods of use |
| WO2009055730A1 (en) * | 2007-10-25 | 2009-04-30 | Genentech, Inc. | Process for making thienopyrimidine compounds |
| GB0721095D0 (en) | 2007-10-26 | 2007-12-05 | Piramed Ltd | Pharmaceutical compounds |
| US20100093702A1 (en) * | 2008-10-13 | 2010-04-15 | Barbay J Kent | METHYLENE AMINES OF THIENO[2,3-d]PYRIMIDINE AND THEIR USE AS ADENOSINE A2a RECEPTOR ANTAGONISTS |
| US20100093714A1 (en) * | 2008-10-13 | 2010-04-15 | Devraj Chakravarty | AMIDES OF THIENO[2,3-d]PYRIMIDINE AND THEIR USE AS ADENOSINE A2a RECEPTOR ANTAGONISTS |
| ES2665277T3 (es) * | 2009-03-13 | 2018-04-25 | Katholieke Universiteit Leuven K.U. Leuven R&D | Análogos de purina y su uso como agentes inmunosupresores |
| EP2451811A1 (en) * | 2009-05-27 | 2012-05-16 | F. Hoffmann-La Roche AG | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| MX2011012520A (es) * | 2009-05-27 | 2011-12-12 | Hoffmann La Roche | Compuestos inhibidores de pi3k de pirimidina biciclicos selectivos para p110 delta y metodos de uso de los mismos. |
| EP2595993B1 (en) | 2010-07-23 | 2018-04-18 | President and Fellows of Harvard College | Tricyclic proteasome activity enhancing compounds |
| US9220715B2 (en) | 2010-11-08 | 2015-12-29 | Omeros Corporation | Treatment of addiction and impulse-control disorders using PDE7 inhibitors |
| NZ628055A (en) * | 2010-11-08 | 2016-03-31 | Omeros Corp | Treatment of addiction and impulse-control disorders using pde7 inhibitors |
| AR090037A1 (es) * | 2011-11-15 | 2014-10-15 | Xention Ltd | Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio |
| IN2014CN04558A (cg-RX-API-DMAC7.html) | 2011-11-23 | 2015-09-18 | Cancer Rec Tech Ltd | |
| JP2015513317A (ja) * | 2012-01-25 | 2015-05-07 | プロテオステイシス セラピューティクス，インコーポレイテッド | プロテアソーム活性を増強する化合物 |
| AU2013202368B2 (en) * | 2012-01-25 | 2016-06-16 | Proteostasis Therapeutics, Inc. | Proteasome activity modulating compounds |
| LT3415517T (lt) | 2012-09-28 | 2022-06-10 | Takeda Pharmaceutical Company Limited | Kristalinė 1-(4-(1-(2,6-difluorbenzil)-5-dimetilaminometil-3-(6-metoksipiridazin-3-il)-2,4-diokso-1,2,3,4- tetrahidrotieno(2,3-d)pirimidin-6-il)fenil)-3-metoksikarbamido forma |
| FR3037957B1 (fr) * | 2015-06-23 | 2019-01-25 | Les Laboratoires Servier | Nouveaux derives d'hydroxyester, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| CN108135906A (zh) * | 2015-07-24 | 2018-06-08 | 路易斯维尔大学研究基金会有限公司 | 治病化合物、组合物、方法、及化合物制备方法 |
| CN115279769A (zh) | 2019-10-10 | 2022-11-01 | 梦欧文科学有限责任公司 | N-(4-(1-(2,6-二氟苄基)-5-((二甲基氨基)甲基)-3-(6-甲氧基-3-哒嗪基)-2,4-二氧代-1,2,3,4-四氢噻吩并[2,3-d]嘧啶-6-基)苯基)-n’-甲氧基脲的结晶形式 |
| CN115232146A (zh) * | 2022-08-04 | 2022-10-25 | 山东大学 | 一种2-氨基噻吩并[2,3-d]嘧啶类化合物及其制备方法和应用 |
| EP4572765A1 (en) | 2022-08-18 | 2025-06-25 | Mitodicure GmbH | Use of a therapeutic agent with phosphodiesterase-7 inhibitory activity for the treatment and prevention of diseases associated with chronic fatigue, exhaustion and/or exertional intolerance |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4008726A1 (de) * | 1990-03-19 | 1991-09-26 | Basf Ag | Thieno(2,3-d)pyrimidinderivate |
| US5869486A (en) * | 1995-02-24 | 1999-02-09 | Ono Pharmaceutical Co., Ltd. | Fused pyrimidines and pyriazines as pharmaceutical compounds |
| JPH1087492A (ja) * | 1996-06-25 | 1998-04-07 | Ono Pharmaceut Co Ltd | 一酸化窒素産生阻害剤 |
| DE19644228A1 (de) * | 1996-10-24 | 1998-04-30 | Merck Patent Gmbh | Thienopyrimidine |
| US6133271A (en) * | 1998-11-19 | 2000-10-17 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure thienopyrimidine derivatives |
| DE19953024A1 (de) * | 1999-11-04 | 2001-05-10 | Merck Patent Gmbh | Isoxazolderivate als Phosphodiesterase VII-Hemmer |
| DE19954707A1 (de) * | 1999-11-13 | 2001-05-17 | Merck Patent Gmbh | Imidazolverbindungen als Phosphodiesterase VII-Hemmer |
| CN1458933A (zh) * | 2000-09-29 | 2003-11-26 | 日本曹达株式会社 | 噻吩并嘧啶化合物及其盐以及其制备方法 |
| EP1193261A1 (en) * | 2000-10-02 | 2002-04-03 | Warner-Lambert Company | New thiadiazoles and their use as phosphodiesterase-7 inhibitors |
| WO2002088138A1 (en) * | 2001-04-30 | 2002-11-07 | Bayer Corporation | Novel 4-amino-5,6-substituted thiopheno[2,3-d]pyrimidines |
| EP1348701A1 (en) * | 2002-03-28 | 2003-10-01 | Warner-Lambert Company LLC | (2,4-disubstituted-thiazol-5-yl) amine compounds as PDE7 inhibitors |
-
2003
- 2003-01-23 ES ES200300172A patent/ES2217956B1/es not_active Expired - Fee Related
-
2004
- 2004-01-23 AT AT04704579T patent/ATE365742T1/de not_active IP Right Cessation
- 2004-01-23 EP EP04704579A patent/EP1590352B1/en not_active Expired - Lifetime
- 2004-01-23 ES ES04704579T patent/ES2289475T3/es not_active Expired - Lifetime
- 2004-01-23 DE DE602004007239T patent/DE602004007239T2/de not_active Expired - Lifetime
- 2004-01-23 JP JP2006500010A patent/JP2006515604A/ja active Pending
- 2004-01-23 US US10/542,940 patent/US7662814B2/en not_active Expired - Fee Related
- 2004-01-23 WO PCT/EP2004/000584 patent/WO2004065391A1/en not_active Ceased
- 2004-01-23 CN CN200480007362A patent/CN100582112C/zh not_active Expired - Fee Related