KR20110031355A - 1,2―이치환된 헤테로사이클릭 화합물 - Google Patents
1,2―이치환된 헤테로사이클릭 화합물 Download PDFInfo
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- KR20110031355A KR20110031355A KR1020117001942A KR20117001942A KR20110031355A KR 20110031355 A KR20110031355 A KR 20110031355A KR 1020117001942 A KR1020117001942 A KR 1020117001942A KR 20117001942 A KR20117001942 A KR 20117001942A KR 20110031355 A KR20110031355 A KR 20110031355A
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- South Korea
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- compound
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- unsubstituted
- alkyl
- cycloalkyl
- Prior art date
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- 0 CC(C)(C(*)=C1c(cc2)ccc2OCc2ccc(cccc3)c3n2)NC1=O Chemical compound CC(C)(C(*)=C1c(cc2)ccc2OCc2ccc(cccc3)c3n2)NC1=O 0.000 description 3
- FTVQPKZMAUWPTG-VOTSOKGWSA-N CC(C)(/C=C/C(c(cc1C#N)ccc1OC)=O)O Chemical compound CC(C)(/C=C/C(c(cc1C#N)ccc1OC)=O)O FTVQPKZMAUWPTG-VOTSOKGWSA-N 0.000 description 1
- IFTSCFOKLYJPFT-VOTSOKGWSA-N CC(C)(/C=C/C(c(cc1Cl)ccc1OC)O)O Chemical compound CC(C)(/C=C/C(c(cc1Cl)ccc1OC)O)O IFTSCFOKLYJPFT-VOTSOKGWSA-N 0.000 description 1
- KSTYPHCVGMXEIL-UHFFFAOYSA-N CC(C)(C#CC(c(cc1)ccc1[N+]([O-])=O)=O)O Chemical compound CC(C)(C#CC(c(cc1)ccc1[N+]([O-])=O)=O)O KSTYPHCVGMXEIL-UHFFFAOYSA-N 0.000 description 1
- XBHPAQWQSFPQRD-UHFFFAOYSA-N CC(C)(C(C#N)=O)Br Chemical compound CC(C)(C(C#N)=O)Br XBHPAQWQSFPQRD-UHFFFAOYSA-N 0.000 description 1
- NFALLYORLKWHHP-UHFFFAOYSA-N CC(C)(C(C1)C=C1C(c(cc1Cl)ccc1OC)=O)O Chemical compound CC(C)(C(C1)C=C1C(c(cc1Cl)ccc1OC)=O)O NFALLYORLKWHHP-UHFFFAOYSA-N 0.000 description 1
- MBQFKKSDEQLNBN-UHFFFAOYSA-N CC(C)(C(O)=C1c(cc2)ccc2OCc2nc(cccc3)c3cc2)NC1=O Chemical compound CC(C)(C(O)=C1c(cc2)ccc2OCc2nc(cccc3)c3cc2)NC1=O MBQFKKSDEQLNBN-UHFFFAOYSA-N 0.000 description 1
- KITCZNNLGGJVJK-UHFFFAOYSA-N CC(C)(C(c(cc1)ccc1OC)=C1c(cc2)ccc2OCc2nc(cccc3)c3cc2)N(C)C1=O Chemical compound CC(C)(C(c(cc1)ccc1OC)=C1c(cc2)ccc2OCc2nc(cccc3)c3cc2)N(C)C1=O KITCZNNLGGJVJK-UHFFFAOYSA-N 0.000 description 1
- NUGFQFLYXIDCAQ-UHFFFAOYSA-N CC(C)(C1=O)OC(c(cc2)ccc2OC)=C1Br Chemical compound CC(C)(C1=O)OC(c(cc2)ccc2OC)=C1Br NUGFQFLYXIDCAQ-UHFFFAOYSA-N 0.000 description 1
- YXHNVOTVRFNVFC-UHFFFAOYSA-N CC(C)(C1=O)OC(c2c[s]cn2)=C1c(cc1)ccc1OCc1nc(cccc2)c2cc1 Chemical compound CC(C)(C1=O)OC(c2c[s]cn2)=C1c(cc1)ccc1OCc1nc(cccc2)c2cc1 YXHNVOTVRFNVFC-UHFFFAOYSA-N 0.000 description 1
- WHZZVEFGRIRYSE-UHFFFAOYSA-N CC(C)(C1=O)OC(c2ccccc2)=C1c(cc1)ccc1OCc1nc(cccc2)c2cc1 Chemical compound CC(C)(C1=O)OC(c2ccccc2)=C1c(cc1)ccc1OCc1nc(cccc2)c2cc1 WHZZVEFGRIRYSE-UHFFFAOYSA-N 0.000 description 1
- DJSMFPZOATUYGQ-UHFFFAOYSA-N CC1(C)OC(c(cc2)cc(C#N)c2OC)=CC1=O Chemical compound CC1(C)OC(c(cc2)cc(C#N)c2OC)=CC1=O DJSMFPZOATUYGQ-UHFFFAOYSA-N 0.000 description 1
- MKMDTXXWHSHEOI-UHFFFAOYSA-N CC1(C)OC(c(cc2)ccc2Cl)=CC1=O Chemical compound CC1(C)OC(c(cc2)ccc2Cl)=CC1=O MKMDTXXWHSHEOI-UHFFFAOYSA-N 0.000 description 1
- RRDVIJBMDMEAIG-UHFFFAOYSA-N CC1(C)OC(c2c[s]cn2)=CC1=O Chemical compound CC1(C)OC(c2c[s]cn2)=CC1=O RRDVIJBMDMEAIG-UHFFFAOYSA-N 0.000 description 1
- OKCONEOGVGNUDS-UHFFFAOYSA-N CC1(C)OC(c2ccncc2)=CC1=O Chemical compound CC1(C)OC(c2ccncc2)=CC1=O OKCONEOGVGNUDS-UHFFFAOYSA-N 0.000 description 1
- OKGLKHSQLFEZIJ-UHFFFAOYSA-N CN(C(c1cc2n[o]nc2cc1)=O)OC Chemical compound CN(C(c1cc2n[o]nc2cc1)=O)OC OKGLKHSQLFEZIJ-UHFFFAOYSA-N 0.000 description 1
- CLOVVBXACYGJKV-UHFFFAOYSA-N COC(C1(CC1)OC(Cc(cc1)ccc1OCc1ccc(cccc2)c2n1)=O)=O Chemical compound COC(C1(CC1)OC(Cc(cc1)ccc1OCc1ccc(cccc2)c2n1)=O)=O CLOVVBXACYGJKV-UHFFFAOYSA-N 0.000 description 1
- KTYXSXUKPAXKOW-UHFFFAOYSA-N N#Cc1cc2n[o]nc2cc1 Chemical compound N#Cc1cc2n[o]nc2cc1 KTYXSXUKPAXKOW-UHFFFAOYSA-N 0.000 description 1
- TYVYWZSCPZCMNF-UHFFFAOYSA-N O=C(Cc(cc1)ccc1OCc1nc2ccccc2cc1)Cl Chemical compound O=C(Cc(cc1)ccc1OCc1nc2ccccc2cc1)Cl TYVYWZSCPZCMNF-UHFFFAOYSA-N 0.000 description 1
- RMAHGMDNLBUFEF-UHFFFAOYSA-N O=C1C(c(cc2)ccc2OCc2nc3ccccc3cc2)=C(c2ccncc2)OC11CCCC1 Chemical compound O=C1C(c(cc2)ccc2OCc2nc3ccccc3cc2)=C(c2ccncc2)OC11CCCC1 RMAHGMDNLBUFEF-UHFFFAOYSA-N 0.000 description 1
- MJDRELIYCROYTK-UHFFFAOYSA-N O=C1OC2(CC2)C(c2ccncc2)=C1c(cc1)ccc1OCc1nc(cccc2)c2cc1 Chemical compound O=C1OC2(CC2)C(c2ccncc2)=C1c(cc1)ccc1OCc1nc(cccc2)c2cc1 MJDRELIYCROYTK-UHFFFAOYSA-N 0.000 description 1
- WZUFYJFTOVGJJT-UHFFFAOYSA-N OC(c1cc2n[o]nc2cc1)=O Chemical compound OC(c1cc2n[o]nc2cc1)=O WZUFYJFTOVGJJT-UHFFFAOYSA-N 0.000 description 1
- BBZAEXIYWVZCGQ-UHFFFAOYSA-N OC1(CCCC1)C#CC(c1ccncc1)=O Chemical compound OC1(CCCC1)C#CC(c1ccncc1)=O BBZAEXIYWVZCGQ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7559408P | 2008-06-25 | 2008-06-25 | |
| US61/075,594 | 2008-06-25 | ||
| US10916208P | 2008-10-28 | 2008-10-28 | |
| US61/109,162 | 2008-10-28 | ||
| US13886608P | 2008-12-18 | 2008-12-18 | |
| US61/138,866 | 2008-12-18 | ||
| US17641309P | 2009-05-07 | 2009-05-07 | |
| US61/176,413 | 2009-05-07 |
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| KR20110031355A true KR20110031355A (ko) | 2011-03-25 |
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| UY32730A (es) | 2009-06-26 | 2011-01-31 | Novartis Ag | Inhibidores de cyp17 |
| US8883788B2 (en) | 2010-08-04 | 2014-11-11 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring compound |
| EP2601192B1 (en) * | 2010-08-04 | 2017-03-01 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compounds |
| RU2603140C2 (ru) | 2010-09-20 | 2016-11-20 | Айронвуд Фармасьютикалз, Инк. | Соединения имидазотриазинона |
| CN107141309A (zh) | 2011-01-11 | 2017-09-08 | 桑诺维恩药品公司 | 杂芳基化合物及其使用方法 |
| CN103476757A (zh) | 2011-02-18 | 2013-12-25 | 阿勒根公司 | 作为磷酸二酯酶10(pde10a)的抑制剂的取代的6,7-二烷氧基-3-异喹啉醇衍生物 |
| AU2012249421B9 (en) | 2011-04-28 | 2015-10-22 | Novartis Ag | 17alpha-hydroxylase/C17,20-lyase inhibitors |
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| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
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| TW201512201A (zh) * | 2013-03-14 | 2015-04-01 | Forum Pharmaceuticals Inc | 化合物的多晶型及鹽類 |
| US9464076B2 (en) | 2013-03-15 | 2016-10-11 | Daiichi Sankyo Company, Limited | Benzothiophene derivative |
| TWI634114B (zh) * | 2013-05-08 | 2018-09-01 | 永恒生物科技公司 | 作為激酶抑制劑之呋喃酮化合物 |
| SG11201509186TA (en) | 2013-06-27 | 2016-01-28 | Pfizer | Heteroaromatic compounds and their use as dopamine d1 ligands |
| WO2015006689A1 (en) | 2013-07-12 | 2015-01-15 | University Of South Alabama | Treatment and diagnosis of cancer and precancerous conditions using pde10a inhibitors and methods to measure pde10a expression |
| US9200016B2 (en) | 2013-12-05 | 2015-12-01 | Allergan, Inc. | Substituted 6, 7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (PDE 10A) |
| MX382781B (es) | 2014-04-02 | 2025-03-13 | Intermune Inc | Piridinonas anti-fibroticas. |
| CN104211638A (zh) * | 2014-08-13 | 2014-12-17 | 李增 | 一种脂肪氨基取代的芸香碱类衍生物及其制备和作为抗阿尔兹海默症的药物中的应用 |
| CN104610134B (zh) * | 2015-01-29 | 2017-01-25 | 安徽星宇化工有限公司 | 一种6‑甲基‑2‑吡啶基甲醇的制备方法 |
| US10738035B2 (en) | 2015-05-13 | 2020-08-11 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| US10179131B2 (en) * | 2015-07-13 | 2019-01-15 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| JP6904970B2 (ja) | 2016-03-07 | 2021-07-21 | エナンタ ファーマシューティカルズ インコーポレイテッド | B型肝炎抗ウイルス剤 |
| US11124509B2 (en) | 2017-03-23 | 2021-09-21 | Clavius Pharmaceuticals, LLC. | Tri-substituted imidazoles for the inhibition of TGF beta and methods of treatment |
| EP3612522A4 (en) | 2017-04-18 | 2021-07-07 | Celgene Quanticel Research, Inc. | THERAPEUTIC COMPOUNDS |
| US10952978B2 (en) | 2017-08-28 | 2021-03-23 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| US11058678B2 (en) | 2018-01-22 | 2021-07-13 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| WO2019191166A1 (en) | 2018-03-29 | 2019-10-03 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| US12077548B2 (en) | 2018-08-22 | 2024-09-03 | Clavius Pharmaceuticals, LLC. | Substituted imidazoles for the inhibition of TGF-β and methods of treatment |
| UY38383A (es) | 2018-09-21 | 2020-04-30 | Enanta Pharm Inc | Heterociclos funcionalizados como agentes antivirales |
| US11198693B2 (en) | 2018-11-21 | 2021-12-14 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| WO2020113094A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| WO2020247444A1 (en) | 2019-06-03 | 2020-12-10 | Enanta Pharmaceuticals, Inc, | Hepatitis b antiviral agents |
| WO2020247561A1 (en) | 2019-06-04 | 2020-12-10 | Enanta Pharmaceuticals, Inc, | Hepatitis b antiviral agents |
| WO2020247575A1 (en) | 2019-06-04 | 2020-12-10 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| US11738019B2 (en) | 2019-07-11 | 2023-08-29 | Enanta Pharmaceuticals, Inc. | Substituted heterocycles as antiviral agents |
| US11236108B2 (en) | 2019-09-17 | 2022-02-01 | Enanta Pharmaceuticals, Inc. | Functionalized heterocycles as antiviral agents |
| KR102811543B1 (ko) | 2019-10-16 | 2025-05-23 | 삼성디스플레이 주식회사 | 유기 전계 발광 소자 및 유기 전계 발광 소자용 다환 화합물 |
| WO2021188414A1 (en) | 2020-03-16 | 2021-09-23 | Enanta Pharmaceuticals, Inc. | Functionalized heterocyclic compounds as antiviral agents |
| TW202304303A (zh) * | 2021-04-13 | 2023-02-01 | 美商富曼西公司 | 殺真菌之吡啶酮 |
| WO2023059224A1 (en) | 2021-10-09 | 2023-04-13 | Joint Stock Company "Pharmasyntez" | A new class of antiviral drugs |
| US11993580B1 (en) | 2022-12-02 | 2024-05-28 | Neumora Therapeutics, Inc. | Methods of treating neurological disorders |
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| YU4403A (sh) * | 2000-07-27 | 2006-05-25 | F. Hoffmann-La Roche Ag. | Derivati 3-indolil-4-fenil-1h-pirol-2,5-diona, kao inhibitori glikogen sintaza kinaze-3 beta |
| US20030032579A1 (en) | 2001-04-20 | 2003-02-13 | Pfizer Inc. | Therapeutic use of selective PDE10 inhibitors |
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| UA86283C2 (uk) * | 2005-01-07 | 2009-04-10 | Пфайзер Продактс Инк. | Гетероароматичні сполуки хіноліну і їх застосування як інгібіторів pde10 |
| JP2007145819A (ja) * | 2005-10-28 | 2007-06-14 | Tanabe Seiyaku Co Ltd | 医薬組成物 |
| NL2000397C2 (nl) | 2006-01-05 | 2007-10-30 | Pfizer Prod Inc | Bicyclische heteroarylverbindingen als PDE10 inhibitoren. |
| EP1845098A1 (en) | 2006-03-29 | 2007-10-17 | Ferrer Internacional, S.A. | Imidazo[1,2-b]pyridazines, their processes of preparation and their use as GABA receptor ligands |
| JP2009535394A (ja) | 2006-05-02 | 2009-10-01 | ファイザー・プロダクツ・インク | Pde10阻害剤としての二環式ヘテロアリール化合物 |
| WO2008033455A2 (en) | 2006-09-13 | 2008-03-20 | The Institutes For Pharmaceutical Discovery, Llc | Biphenyl and heteroaryl phenyl derivatives as protein tyrosine phosphatases inhibitors |
| JP5079011B2 (ja) * | 2006-10-19 | 2012-11-21 | エフ.ホフマン−ラ ロシュ アーゲー | 糖尿病のための11β−HSD1阻害剤としてのイミダゾロン及びイミダゾリジノン誘導体 |
| FR2928924B1 (fr) | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, leur preparation et leur application en therapeutique |
| CN102131801B (zh) | 2008-06-25 | 2015-04-08 | 福拉姆医药股份有限公司 | 1,2-二取代的杂环化合物 |
| KR101662699B1 (ko) | 2009-05-07 | 2016-10-05 | 포럼 파마슈티칼즈 인크. | 페녹시메틸 헤테로고리 화합물 |
| IN2012DN02493A (https=) | 2009-09-03 | 2015-08-28 | Allergan Inc | |
| ES2879314T3 (es) | 2010-08-18 | 2021-11-22 | Biosplice Therapeutics Inc | Dicetonas e hidroxicetonas como activadores de la vía de señalización de catenina |
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- 2009-06-24 KR KR1020117001942A patent/KR20110031355A/ko not_active Abandoned
- 2009-06-24 MX MX2011000175A patent/MX2011000175A/es active IP Right Grant
- 2009-06-24 WO PCT/US2009/048426 patent/WO2009158393A1/en not_active Ceased
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- 2009-06-24 EP EP09770926.5A patent/EP2297133B1/en active Active
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- 2009-06-25 CN CN2009801332730A patent/CN102131800A/zh active Pending
- 2009-06-25 KR KR1020117001893A patent/KR20110029153A/ko not_active Withdrawn
- 2009-06-25 CA CA2729275A patent/CA2729275A1/en not_active Abandoned
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- 2009-06-25 US US13/001,359 patent/US8481534B2/en not_active Expired - Fee Related
- 2009-06-25 WO PCT/US2009/048617 patent/WO2009158473A1/en not_active Ceased
- 2009-06-25 TW TW103127120A patent/TWI542590B/zh not_active IP Right Cessation
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- 2011-11-07 US US13/290,527 patent/US8466148B2/en not_active Expired - Fee Related
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- 2013-06-17 US US13/919,516 patent/US20140038965A1/en not_active Abandoned
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