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
- C07D471/04—Ortho-condensed systems
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Applications Claiming Priority (8)
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| US7559408P | 2008-06-25 | 2008-06-25 | |
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| 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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| BRPI0914772A2 (pt) | 2008-06-25 | 2015-10-20 | Envivo Pharmaceuticals Inc | compostos heterocíclicos 1,2-dissubstituídos |
| CN105125547A (zh) * | 2009-05-07 | 2015-12-09 | 费瑞姆医药有限公司 | 苯氧基甲基杂环化合物 |
| WO2010149755A1 (en) | 2009-06-26 | 2010-12-29 | Novartis Ag | 1, 3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17 |
| US9029536B2 (en) * | 2010-08-04 | 2015-05-12 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compounds |
| EP2602255B1 (en) | 2010-08-04 | 2017-04-26 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring compound |
| EP2619208B1 (en) | 2010-09-20 | 2016-11-09 | Ironwood Pharmaceuticals, Inc. | Imidazotriazinone compounds |
| US8765760B2 (en) | 2011-01-11 | 2014-07-01 | Sunovion Pharmaceuticals, Inc. | [1,2,4] triazol [1,5-a] pyrazines useful as inhibitors of phosphodiesterases |
| CA2827724A1 (en) | 2011-02-18 | 2012-08-23 | Allergan, Inc. | Substituted 6,7-dialkoxy-3-isoquinolinol derivatives as inhibitors of phosphodiesterase 10 (pde10a) |
| US9029399B2 (en) | 2011-04-28 | 2015-05-12 | Novartis Ag | 17α-hydroxylase/C17,20-lyase inhibitors |
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| 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 |
| DK3013813T3 (da) | 2013-06-27 | 2019-06-03 | Pfizer | Heteroaromatiske forbindelser og anvendelse deraf som dopamin-d1-ligander |
| US10039764B2 (en) | 2013-07-12 | 2018-08-07 | 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 |
| WO2016183266A1 (en) | 2015-05-13 | 2016-11-17 | Enanta Pharmaceuticals, Inc. | Ehpatitis b antiviral agents |
| US10179131B2 (en) * | 2015-07-13 | 2019-01-15 | Enanta Pharmaceuticals, Inc. | Hepatitis B antiviral agents |
| KR102398439B1 (ko) | 2016-03-07 | 2022-05-16 | 이난타 파마슈티칼스, 인코포레이티드 | B형 간염 항바이러스제 |
| WO2019005241A1 (en) | 2017-03-23 | 2019-01-03 | Clavius Pharmaceuticals, Llc | TRI-SUBSTITUTED IMIDAZOLES FOR INHIBITION OF TGF-BETA AND METHODS OF TREATMENT |
| WO2018195155A1 (en) | 2017-04-18 | 2018-10-25 | Celgene Quanticel Research, Inc. | Therapeutic compounds |
| SG11202001685TA (en) | 2017-08-28 | 2020-03-30 | Enanta Pharm 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 |
| WO2020041562A1 (en) | 2018-08-22 | 2020-02-27 | Clavius Pharmaceuticals, Llc | Substituted imidazoles for the inhibition of tgf-beta and methods of treatment |
| JP2022500466A (ja) | 2018-09-21 | 2022-01-04 | 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 | 抗ウイルス剤としての官能化複素環 |
| IL283190B2 (en) | 2018-11-21 | 2025-08-01 | Enanta Pharm Inc | Functionalized heterocycles as antiviral agents |
| CA3121202A1 (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 |
| WO2020247575A1 (en) | 2019-06-04 | 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 |
| 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 |
| EP4626878A1 (en) | 2022-12-02 | 2025-10-08 | Neumora Therapeutics, Inc. | Methods of treating neurological disorders |
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| CA2417277A1 (en) * | 2000-07-27 | 2002-02-07 | F. Hoffmann-La Roche Ag | 3-indolyl-4-phenyl-1h-pyrrole-2,5-dione derivatives as inhibitors of glycogen synthase kinase-3.beta. |
| US20030032579A1 (en) * | 2001-04-20 | 2003-02-13 | Pfizer Inc. | Therapeutic use of selective PDE10 inhibitors |
| WO2004002484A1 (ja) | 2002-06-26 | 2004-01-08 | Kyowa Hakko Kogyo Co., Ltd. | ホスホジエステラーゼ阻害剤 |
| KR100896380B1 (ko) | 2005-01-07 | 2009-05-08 | 화이자 프로덕츠 인코포레이티드 | 헤테로방향족 퀴놀린 화합물 및 pde10 저해제로서의그의 용도 |
| 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 |
| US20090176829A1 (en) | 2006-05-02 | 2009-07-09 | Pfizer Inc | Bicyclic heteroaryl compounds as pde10 inhibitors |
| WO2008033455A2 (en) | 2006-09-13 | 2008-03-20 | The Institutes For Pharmaceutical Discovery, Llc | Biphenyl and heteroaryl phenyl derivatives as protein tyrosine phosphatases inhibitors |
| CN101553474B (zh) * | 2006-10-19 | 2013-02-27 | 霍夫曼-拉罗奇有限公司 | 作为糖尿病用11b-HSD1抑制剂的咪唑啉酮和咪唑烷酮衍生物 |
| 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 |
| BRPI0914772A2 (pt) | 2008-06-25 | 2015-10-20 | Envivo Pharmaceuticals Inc | compostos heterocíclicos 1,2-dissubstituídos |
| CN105125547A (zh) * | 2009-05-07 | 2015-12-09 | 费瑞姆医药有限公司 | 苯氧基甲基杂环化合物 |
| AU2010289353B2 (en) * | 2009-09-03 | 2016-12-08 | Allergan, Inc. | Compounds as tyrosine kinase modulators |
| RU2592694C2 (ru) * | 2010-08-18 | 2016-07-27 | СЭМЬЮМЕД, ЭлЭлСи | Дикетоны и гидроксикетоны в качестве активатора сигнального пути катенина |
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2009
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- 2009-06-24 KR KR1020117001942A patent/KR20110031355A/ko not_active Abandoned
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- 2009-06-24 CN CN200980133288.7A patent/CN102131801B/zh not_active Expired - Fee Related
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- 2009-06-24 EP EP09770926.5A patent/EP2297133B1/en active Active
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- 2009-06-24 WO PCT/US2009/048426 patent/WO2009158393A1/en not_active Ceased
- 2009-06-25 EP EP09771005A patent/EP2303863A1/en not_active Withdrawn
- 2009-06-25 TW TW103127120A patent/TWI542590B/zh not_active IP Right Cessation
- 2009-06-25 US US13/001,359 patent/US8481534B2/en not_active Expired - Fee Related
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- 2009-06-25 TW TW098121521A patent/TWI458723B/zh not_active IP Right Cessation
- 2009-06-25 CA CA2729275A patent/CA2729275A1/en not_active Abandoned
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- 2009-06-25 CN CN2009801332730A patent/CN102131800A/zh active Pending
- 2009-06-25 WO PCT/US2009/048617 patent/WO2009158473A1/en not_active Ceased
- 2009-06-25 BR BRPI0913958A patent/BRPI0913958A2/pt not_active IP Right Cessation
- 2009-06-25 JP JP2011516650A patent/JP2011526295A/ja active Pending
- 2009-06-25 KR KR1020117001893A patent/KR20110029153A/ko not_active Withdrawn
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- 2011-11-07 US US13/290,527 patent/US8466148B2/en not_active Expired - Fee Related
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2013
- 2013-06-17 US US13/919,516 patent/US20140038965A1/en not_active Abandoned
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2014
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