JP6955482B2 - Tnfアルファの修飾因子として有用なヘテロ環化合物 - Google Patents
Tnfアルファの修飾因子として有用なヘテロ環化合物 Download PDFInfo
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- JP6955482B2 JP6955482B2 JP2018506144A JP2018506144A JP6955482B2 JP 6955482 B2 JP6955482 B2 JP 6955482B2 JP 2018506144 A JP2018506144 A JP 2018506144A JP 2018506144 A JP2018506144 A JP 2018506144A JP 6955482 B2 JP6955482 B2 JP 6955482B2
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- Prior art keywords
- chloro
- amino
- ethyl
- quinoline
- pyrimidin
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- 0 **Ic1c2nc(*)nc(*)c2nc(*)c1* Chemical compound **Ic1c2nc(*)nc(*)c2nc(*)c1* 0.000 description 4
- YFEBQTVOEZGSMG-UHFFFAOYSA-N Brc1cnc(C2=CCCC2)nc1 Chemical compound Brc1cnc(C2=CCCC2)nc1 YFEBQTVOEZGSMG-UHFFFAOYSA-N 0.000 description 1
- SBWHZSGCGUCUMO-UHFFFAOYSA-N CC(C)(c(nc1)ncc1-c(ccc1nc(C(Nc2cccnc2)=O)c2Cl)cc1c2Cl)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1nc(C(Nc2cccnc2)=O)c2Cl)cc1c2Cl)O SBWHZSGCGUCUMO-UHFFFAOYSA-N 0.000 description 1
- SJXPIQHATIAKHP-UHFFFAOYSA-N CC(C)(c(nc1)ncc1-c(ccc1nc(C)c2Cl)cc1c2NCc(cc(C=C)cc1)c1F)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1nc(C)c2Cl)cc1c2NCc(cc(C=C)cc1)c1F)O SJXPIQHATIAKHP-UHFFFAOYSA-N 0.000 description 1
- FQQUQAIHJQUNEH-UHFFFAOYSA-N CC(C)(c(nc1)ncc1-c(ccc1nc(C)c2Cl)cc1c2NCc(cc(CCO)cc1)c1F)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1nc(C)c2Cl)cc1c2NCc(cc(CCO)cc1)c1F)O FQQUQAIHJQUNEH-UHFFFAOYSA-N 0.000 description 1
- OVZRAIKEAOFZAQ-UHFFFAOYSA-N CC(C)(c(nc1)ncc1-c(ccc1nc(C)c2Cl)cc1c2NCc(cc(cc1)C(C)=O)c1F)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1nc(C)c2Cl)cc1c2NCc(cc(cc1)C(C)=O)c1F)O OVZRAIKEAOFZAQ-UHFFFAOYSA-N 0.000 description 1
- OMYIRGIQYPVPLE-LODFRUGASA-N CC(C)(c(nc1)ncc1-c(ccc1ncc2Cl)cc1c2NCc(cc(/C=N/O)cc1)c1F)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1ncc2Cl)cc1c2NCc(cc(/C=N/O)cc1)c1F)O OMYIRGIQYPVPLE-LODFRUGASA-N 0.000 description 1
- JJCIFPDUGJAQDX-UHFFFAOYSA-N CC(C)(c(nc1)ncc1-c(ccc1ncc2Cl)cc1c2NCc(cc(cc1)C#Cc2ccccc2)c1F)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1ncc2Cl)cc1c2NCc(cc(cc1)C#Cc2ccccc2)c1F)O JJCIFPDUGJAQDX-UHFFFAOYSA-N 0.000 description 1
- MWYQRUVZEOZNDV-UHFFFAOYSA-N CC(C)(c(nc1)ncc1-c(ccc1ncc2Cl)cc1c2NCc(cc(cc1)C(C)=O)c1F)O Chemical compound CC(C)(c(nc1)ncc1-c(ccc1ncc2Cl)cc1c2NCc(cc(cc1)C(C)=O)c1F)O MWYQRUVZEOZNDV-UHFFFAOYSA-N 0.000 description 1
- ICJQELZRENMBHU-BZSJEYESSA-N CC([C@H](CCC1)CN1C(N)=O)Nc1c(cc(cc2)-c3cnc(C(C)(C)O)nc3)c2ncc1Cl Chemical compound CC([C@H](CCC1)CN1C(N)=O)Nc1c(cc(cc2)-c3cnc(C(C)(C)O)nc3)c2ncc1Cl ICJQELZRENMBHU-BZSJEYESSA-N 0.000 description 1
- SYTCWMIORUIBRU-UHFFFAOYSA-N CC(c(cccc1)c1F)Nc1c(cc(-c2cnc(N3CCN(CC(O)=O)CC3)nc2)nc2)c2ncc1Cl Chemical compound CC(c(cccc1)c1F)Nc1c(cc(-c2cnc(N3CCN(CC(O)=O)CC3)nc2)nc2)c2ncc1Cl SYTCWMIORUIBRU-UHFFFAOYSA-N 0.000 description 1
- OQWARZRXFUWOIC-UHFFFAOYSA-N CC(c(cccc1)c1F)Nc1c(cc(c(Cl)c2)Br)c2ncc1Cl Chemical compound CC(c(cccc1)c1F)Nc1c(cc(c(Cl)c2)Br)c2ncc1Cl OQWARZRXFUWOIC-UHFFFAOYSA-N 0.000 description 1
- UFFNJIPLLOIGNR-UHFFFAOYSA-N CC(c(cccc1)c1F)Nc1c(cc(nc2)OC)c2ncc1Cl Chemical compound CC(c(cccc1)c1F)Nc1c(cc(nc2)OC)c2ncc1Cl UFFNJIPLLOIGNR-UHFFFAOYSA-N 0.000 description 1
- KUEQPBVADBEHPL-UHFFFAOYSA-N CC(c(nc(C(CO)O)cc1)c1F)Nc1c(cc(cc2)Br)c2ncc1 Chemical compound CC(c(nc(C(CO)O)cc1)c1F)Nc1c(cc(cc2)Br)c2ncc1 KUEQPBVADBEHPL-UHFFFAOYSA-N 0.000 description 1
- SNVXEUIVNATGEP-UHFFFAOYSA-N CCC(c(nc(cc1)C(N)=O)c1F)N Chemical compound CCC(c(nc(cc1)C(N)=O)c1F)N SNVXEUIVNATGEP-UHFFFAOYSA-N 0.000 description 1
- XFANWRJXACPLCS-UHFFFAOYSA-N COC(CN(CC1)CCN1c(nc1)ncc1Br)=O Chemical compound COC(CN(CC1)CCN1c(nc1)ncc1Br)=O XFANWRJXACPLCS-UHFFFAOYSA-N 0.000 description 1
- WTFYRNSXWBFWSP-SGZRZGDHSA-N C[C@H](c(cc(cc1)Br)c1F)Nc1c(cc(cc2)C3=CNC(C(C)(C)O)N=C3)c2nc(C)c1Cl Chemical compound C[C@H](c(cc(cc1)Br)c1F)Nc1c(cc(cc2)C3=CNC(C(C)(C)O)N=C3)c2nc(C)c1Cl WTFYRNSXWBFWSP-SGZRZGDHSA-N 0.000 description 1
- HJOJGOQYSKUFAZ-MRXNPFEDSA-N C[C@H](c(cccc1)c1F)Nc1c(cc(cc2)-c3cnc(C(C)(C)O)nc3)c2ncc1C Chemical compound C[C@H](c(cccc1)c1F)Nc1c(cc(cc2)-c3cnc(C(C)(C)O)nc3)c2ncc1C HJOJGOQYSKUFAZ-MRXNPFEDSA-N 0.000 description 1
- WJWRJYKUXCTVBH-CQSZACIVSA-N C[C@H](c1cc(CC(O)=O)ccc1F)Nc1c(cc(cc2)-c3cnc(C(C)(C)O)nc3)c2nc(C)c1Cl Chemical compound C[C@H](c1cc(CC(O)=O)ccc1F)Nc1c(cc(cc2)-c3cnc(C(C)(C)O)nc3)c2nc(C)c1Cl WJWRJYKUXCTVBH-CQSZACIVSA-N 0.000 description 1
- YQZHKDURSGPROF-UHFFFAOYSA-N O=CCC(c(cccc1)c1F)N(C(c1c2cccc1)=O)C2=O Chemical compound O=CCC(c(cccc1)c1F)N(C(c1c2cccc1)=O)C2=O YQZHKDURSGPROF-UHFFFAOYSA-N 0.000 description 1
- ICHXPSPFWNZVTI-UHFFFAOYSA-N OC1(CCCC1)c(nc1)ncc1Br Chemical compound OC1(CCCC1)c(nc1)ncc1Br ICHXPSPFWNZVTI-UHFFFAOYSA-N 0.000 description 1
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562200424P | 2015-08-03 | 2015-08-03 | |
| US62/200,424 | 2015-08-03 | ||
| PCT/US2016/045110 WO2017023905A1 (en) | 2015-08-03 | 2016-08-02 | Heterocyclic compounds useful as modulators of tnf alpha |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018525379A JP2018525379A (ja) | 2018-09-06 |
| JP2018525379A5 JP2018525379A5 (OSRAM) | 2019-08-15 |
| JP6955482B2 true JP6955482B2 (ja) | 2021-10-27 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018506144A Active JP6955482B2 (ja) | 2015-08-03 | 2016-08-02 | Tnfアルファの修飾因子として有用なヘテロ環化合物 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US10865191B2 (OSRAM) |
| EP (1) | EP3331871A1 (OSRAM) |
| JP (1) | JP6955482B2 (OSRAM) |
| KR (1) | KR102697810B1 (OSRAM) |
| CN (1) | CN108137547B (OSRAM) |
| AR (1) | AR105575A1 (OSRAM) |
| AU (1) | AU2016302144B2 (OSRAM) |
| BR (1) | BR112018001960A2 (OSRAM) |
| CA (1) | CA2994717A1 (OSRAM) |
| CL (1) | CL2018000293A1 (OSRAM) |
| CO (1) | CO2018002061A2 (OSRAM) |
| EA (1) | EA033686B1 (OSRAM) |
| HK (1) | HK1252623A1 (OSRAM) |
| IL (1) | IL257154A (OSRAM) |
| MA (1) | MA43512A (OSRAM) |
| MX (1) | MX375341B (OSRAM) |
| PE (1) | PE20181366A1 (OSRAM) |
| SG (1) | SG10201911831RA (OSRAM) |
| TW (1) | TW201718536A (OSRAM) |
| UY (1) | UY36838A (OSRAM) |
| WO (1) | WO2017023905A1 (OSRAM) |
| ZA (1) | ZA201800716B (OSRAM) |
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| US20160304496A1 (en) | 2015-04-17 | 2016-10-20 | Abbvie Inc. | Indazolones as modulators of tnf signaling |
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| US9856253B2 (en) | 2015-04-17 | 2018-01-02 | Abbvie, Inc. | Tricyclic modulators of TNF signaling |
| GB201510758D0 (en) | 2015-06-18 | 2015-08-05 | Ucb Biopharma Sprl | Novel TNFa structure for use in therapy |
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| CN108026050B (zh) | 2015-08-03 | 2021-04-30 | 格兰马克药品股份有限公司 | 作为RORγ调节剂的新型化合物 |
| GB201621907D0 (en) | 2016-12-21 | 2017-02-01 | Ucb Biopharma Sprl And Sanofi | Antibody epitope |
| JOP20190257A1 (ar) * | 2017-04-28 | 2019-10-28 | Novartis Ag | مركبات أريل غير متجانسة ثنائية الحلقة مندمجة 6-6 واستخدامها كمثبطات lats |
| CN111868036A (zh) | 2018-02-09 | 2020-10-30 | 美国政府健康与人类服务部 | 杂环p2y14受体拮抗剂 |
| CN108658977A (zh) * | 2018-04-12 | 2018-10-16 | 苏州康润医药有限公司 | 一种7-溴-1,5-萘啶-3-甲酸的合成方法 |
| BR112022023550A2 (pt) | 2020-05-19 | 2023-01-03 | Bayer Cropscience Ag | (tio)amidas azabicíclicas como compostos fungicidas |
| WO2021249995A1 (en) | 2020-06-10 | 2021-12-16 | Bayer Aktiengesellschaft | Azabicyclyl-substituted heterocycles as fungicides |
| EP4167982A4 (en) | 2020-06-22 | 2024-08-07 | PMV Pharmaceuticals, Inc. | METHODS AND COMPOUNDS FOR RESTORING FUNCTION OF P53 MUTANTS |
| CN115803085A (zh) | 2020-06-27 | 2023-03-14 | 新月生物科学 | 新型细胞代谢调节化合物及用途 |
| ES3026782T3 (en) * | 2020-11-27 | 2025-06-12 | Chiesi Farm Spa | (aza)quinoline 4-amines derivatives as p2x3 inhibitors |
| KR20230155422A (ko) * | 2020-12-22 | 2023-11-10 | 메카니스틱 테라퓨틱스 엘엘씨 | Egfr 및/또는 pi3k 억제제로서의 치환된 아미노벤질헤테로아릴 화합물 |
| EP4410790A4 (en) * | 2021-09-29 | 2025-12-17 | Haihe Biopharma Co Ltd | SOS1 inhibitors with a hexagonal pyridor ring structure |
| WO2023067546A1 (en) * | 2021-10-21 | 2023-04-27 | Satyarx Pharma Innovations Pvt Ltd | Novel bicyclic heteroaryl derivatives as sos1:kras proteinprotein interaction inhibitors |
| US12138243B2 (en) | 2021-12-31 | 2024-11-12 | Crescenta Biosciences | Antiviral use of FABP4 modulating compounds |
| CN114605409B (zh) * | 2022-04-01 | 2024-04-02 | 苏州睿尔思科技有限公司 | 一种4-羟基-1,5-萘啶类配体的生产制备方法 |
| CN114751858B (zh) * | 2022-04-20 | 2023-09-12 | 沈阳药科大学 | 含有喹啉基的氨甲环酸衍生物及其制备与应用 |
| CN117024404A (zh) * | 2022-05-10 | 2023-11-10 | 四川汇宇制药股份有限公司 | 苯并吡啶衍生物及其用途 |
| AR133582A1 (es) * | 2023-08-18 | 2025-10-15 | Incyte Corp | Heterociclos bicíclicos como antagonistas de mrgprx2 |
| WO2025147600A1 (en) * | 2024-01-05 | 2025-07-10 | Dewpoint Therapeutics, Inc. | Amino quinoline compounds and uses thereof |
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| US856095A (en) * | 1906-09-01 | 1907-06-04 | Railway Safety Signal Company | Electric semaphore. |
| EP0282959A3 (en) * | 1987-03-17 | 1989-05-31 | Hoechst-Roussel Pharmaceuticals Incorporated | Substituted 9-amino-tetrahydro-acridines and related compounds, a process for their preparation and their use as medicaments |
| DE3917232A1 (de) * | 1989-05-26 | 1990-11-29 | Basf Ag | 4-arylmethamino-2,3-dialkyl-chinoline, ihre verwendung und daraus hergestellte arzneimittel |
| SK14142003A3 (sk) * | 2001-05-31 | 2005-03-04 | Sanofi-Aventis | Aminochinolínové a aminopyridínové deriváty a ich použitie ako adenozínových A3 ligandov |
| WO2003024899A2 (en) * | 2001-09-17 | 2003-03-27 | Bristol-Myers Squibb Company | CYCLIC HYDROXAMIC ACIDS AS INHIBITORS OF MATRIX METALLOPROTEINASES AND/OR TNF-α CONVERTING ENZYME (TACE) |
| WO2003053941A2 (en) * | 2001-12-20 | 2003-07-03 | Bristol-Myers Squibb Company | Barbituric acid derivatives as inhibitors of tnf-alpha converting enzyme (tace) and/or matrix metalloproteinases |
| HUP0105406A3 (en) | 2001-12-21 | 2003-12-29 | Sanofi Aventis | Imidazo[1,2-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
| WO2005009969A1 (en) | 2003-07-31 | 2005-02-03 | Sanofi-Aventis | Aminoquinoline derivatives and their use as adenosine a3 ligands |
| TW200815447A (en) | 2006-06-14 | 2008-04-01 | Astrazeneca Ab | Novel compounds IV |
| CA2725014C (en) * | 2008-05-30 | 2014-06-17 | Amgen Inc. | Inhibitors of pi3 kinase |
| MX342879B (es) * | 2010-07-30 | 2016-10-14 | Oncotherapy Science Inc * | Derivados de quinolina e inhibidores de cinasa de cremallera de leucina embrionica materna que los contienen. |
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| CN104619709B (zh) * | 2012-07-13 | 2016-11-09 | Ucb生物制药私人有限公司 | 作为tnf活性调节剂的咪唑并吡啶衍生物 |
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| US9695179B2 (en) * | 2013-03-14 | 2017-07-04 | Convergene Llc | Methods and compositions for inhibition of bromodomain-containing proteins |
| AR105556A1 (es) | 2015-08-03 | 2017-10-18 | Hoffmann La Roche | Derivados de etinilo |
| CN108026050B (zh) | 2015-08-03 | 2021-04-30 | 格兰马克药品股份有限公司 | 作为RORγ调节剂的新型化合物 |
| GB201513742D0 (en) | 2015-08-03 | 2015-09-16 | Heptares Therapeutics Ltd | Muscarinic agonists |
| EP3436459B1 (en) | 2016-04-01 | 2021-08-25 | UCB Biopharma SRL | Fused pentacyclic imidazole derivatives as modulators of tnf activity |
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| BR112018001960A2 (pt) | 2018-09-18 |
| CN108137547B (zh) | 2021-11-12 |
| US20180222883A1 (en) | 2018-08-09 |
| HK1252623A1 (zh) | 2019-05-31 |
| AU2016302144A1 (en) | 2018-03-22 |
| WO2017023905A1 (en) | 2017-02-09 |
| KR20180031772A (ko) | 2018-03-28 |
| IL257154A (en) | 2018-03-29 |
| EP3331871A1 (en) | 2018-06-13 |
| EA201890165A1 (ru) | 2018-07-31 |
| SG10201911831RA (en) | 2020-02-27 |
| ZA201800716B (en) | 2019-07-31 |
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