JP2019534261A5 - - Google Patents
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- Publication number
- JP2019534261A5 JP2019534261A5 JP2019518440A JP2019518440A JP2019534261A5 JP 2019534261 A5 JP2019534261 A5 JP 2019534261A5 JP 2019518440 A JP2019518440 A JP 2019518440A JP 2019518440 A JP2019518440 A JP 2019518440A JP 2019534261 A5 JP2019534261 A5 JP 2019534261A5
- Authority
- JP
- Japan
- Prior art keywords
- cancer
- salt
- compound according
- acceptable
- methyl
- 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.)
- Granted
Links
- 0 CCC*(CC**c1n*(*)c(C(*=C2)=**2N*)[n]1)C(C(*)(*)*(CC1)CC1(CC*1C2=*CC(C(**)=**3(C)C)=C3C=C2)C1=O)=O Chemical compound CCC*(CC**c1n*(*)c(C(*=C2)=**2N*)[n]1)C(C(*)(*)*(CC1)CC1(CC*1C2=*CC(C(**)=**3(C)C)=C3C=C2)C1=O)=O 0.000 description 3
- MBVCTQKXEGCCCL-UHFFFAOYSA-N CC(O1)=NN(C)C1=O Chemical compound CC(O1)=NN(C)C1=O MBVCTQKXEGCCCL-UHFFFAOYSA-N 0.000 description 1
- HZMBHUAOZYMRMM-UHFFFAOYSA-N CCCN(CCC(N(CC)c(nc12)ccc1[nH]nc2-c1ccc2[nH]nc(C)c2c1)=O)CC(N(CC1)CC=C1c(cc1)ccc1-c1n[n](C)cn1)=O Chemical compound CCCN(CCC(N(CC)c(nc12)ccc1[nH]nc2-c1ccc2[nH]nc(C)c2c1)=O)CC(N(CC1)CC=C1c(cc1)ccc1-c1n[n](C)cn1)=O HZMBHUAOZYMRMM-UHFFFAOYSA-N 0.000 description 1
- GNZLMOPUFWAWCM-UHFFFAOYSA-N CCN(C(C1(C)CN(CC(N(CC2)CC=C2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)ccc1OC(C)C Chemical compound CCN(C(C1(C)CN(CC(N(CC2)CC=C2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)ccc1OC(C)C GNZLMOPUFWAWCM-UHFFFAOYSA-N 0.000 description 1
- QXAXJRFSRONTIN-RMVMEJTISA-N CCN(C(C1)C=Cc2c1c(-c(nc1)ccc1[F]C)n[nH]2)C([C@H]1CN(CC(N(CC2)CCN2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O Chemical compound CCN(C(C1)C=Cc2c1c(-c(nc1)ccc1[F]C)n[nH]2)C([C@H]1CN(CC(N(CC2)CCN2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O QXAXJRFSRONTIN-RMVMEJTISA-N 0.000 description 1
- DCSWJQOSZKSFEZ-UHFFFAOYSA-N CCN(C(C1=CN(CC(N(CC2)CCN2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cn1)ccc1OC Chemical compound CCN(C(C1=CN(CC(N(CC2)CCN2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cn1)ccc1OC DCSWJQOSZKSFEZ-UHFFFAOYSA-N 0.000 description 1
- IAYZAOMOUHPOLI-UHFFFAOYSA-N CCN(C(C1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c1ccc2[o]nc(C)c2c1 Chemical compound CCN(C(C1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c1ccc2[o]nc(C)c2c1 IAYZAOMOUHPOLI-UHFFFAOYSA-N 0.000 description 1
- RUBGBTVEESZOCD-QASNXKAYSA-N CCN(C(C1[C@@H](C)CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)C1)=O)c(nc12)ccc1[nH]nc2-c(c(F)c1)ccc1[ClH]C Chemical compound CCN(C(C1[C@@H](C)CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)C1)=O)c(nc12)ccc1[nH]nc2-c(c(F)c1)ccc1[ClH]C RUBGBTVEESZOCD-QASNXKAYSA-N 0.000 description 1
- NDPMJKQHUDUIKM-SSEXGKCCSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc(C(c(cc2)ccc2OC(C)C)=N)c1N Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc(C(c(cc2)ccc2OC(C)C)=N)c1N NDPMJKQHUDUIKM-SSEXGKCCSA-N 0.000 description 1
- ITMAOYQVJCZFGA-SSEXGKCCSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)cc(OC)c1OC(C)C Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)cc(OC)c1OC(C)C ITMAOYQVJCZFGA-SSEXGKCCSA-N 0.000 description 1
- DVYAVLSWFJARNY-MUUNZHRXSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc12)ccc1[nH]nc2-c(nc1OC)ccc1OC1CC1 Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc12)ccc1[nH]nc2-c(nc1OC)ccc1OC1CC1 DVYAVLSWFJARNY-MUUNZHRXSA-N 0.000 description 1
- MDKYGHNCPWMSJJ-WJOKGBTCSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=N)=O)CC1)=O)c(cc1)cc2c1[nH]nc2-c(cc1)ccc1OC(C)C Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=N)=O)CC1)=O)c(cc1)cc2c1[nH]nc2-c(cc1)ccc1OC(C)C MDKYGHNCPWMSJJ-WJOKGBTCSA-N 0.000 description 1
- CULMORASYYAQGQ-GDLZYMKVSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=N)=O)CC1)=O)c(cc1)cc2c1[nH]nc2-c(nc1N2CCCC2)ccc1F Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=N)=O)CC1)=O)c(cc1)cc2c1[nH]nc2-c(nc1N2CCCC2)ccc1F CULMORASYYAQGQ-GDLZYMKVSA-N 0.000 description 1
- HSLXVKOJYMNMNE-SSEXGKCCSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=N)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)ccc1C#[N]C Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=N)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)ccc1C#[N]C HSLXVKOJYMNMNE-SSEXGKCCSA-N 0.000 description 1
- RRAOYXXXEMFIES-MUUNZHRXSA-O CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=[NH2+])=O)CC1)=O)c(cc12)ccc1[nH]nc2-c(nc1)ccc1C#N Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(/N=C\NC)=[NH2+])=O)CC1)=O)c(cc12)ccc1[nH]nc2-c(nc1)ccc1C#N RRAOYXXXEMFIES-MUUNZHRXSA-O 0.000 description 1
- LYEJXIHOCDMNLO-HHHXNRCGSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(O2)=NN(C)C2=O)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c1ccc(C)nc1 Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c(cc2)ccc2C(O2)=NN(C)C2=O)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c1ccc(C)nc1 LYEJXIHOCDMNLO-HHHXNRCGSA-N 0.000 description 1
- HAJBINBHTWYDAK-MUUNZHRXSA-N CCN(C([C@H]1CN(CC(N(CC2)CC=C2c2ccc(-c3n[n](C)cn3)nc2)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c(cc1)ccc1OC(C)C Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CC=C2c2ccc(-c3n[n](C)cn3)nc2)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c(cc1)ccc1OC(C)C HAJBINBHTWYDAK-MUUNZHRXSA-N 0.000 description 1
- WTKZDLSBVYKJJB-RUZDIDTESA-N CCN(C([C@H]1CN(CC(N(CC2)CCN2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c1ccnc(C)c1 Chemical compound CCN(C([C@H]1CN(CC(N(CC2)CCN2c(nc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c1ccnc(C)c1 WTKZDLSBVYKJJB-RUZDIDTESA-N 0.000 description 1
- KJUGBSAKKMBCRD-LBNVMWSVSA-N CCN(C([C@H]1CN(CC(N(CC2)[C@@H](C)CN2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c(cc1)cnc1OC(C)C Chemical compound CCN(C([C@H]1CN(CC(N(CC2)[C@@H](C)CN2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(nc12)ccc1[nH]nc2-c(cc1)cnc1OC(C)C KJUGBSAKKMBCRD-LBNVMWSVSA-N 0.000 description 1
- KJUGBSAKKMBCRD-LEAFIULHSA-N CCN(C([C@H]1CN(CC(N(CC2)[C@H](C)CN2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)cnc1OC(C)C Chemical compound CCN(C([C@H]1CN(CC(N(CC2)[C@H](C)CN2c(cc2)ccc2-c2n[n](C)cn2)=O)CC1)=O)c(cc1)nc2c1[nH]nc2-c(cc1)cnc1OC(C)C KJUGBSAKKMBCRD-LEAFIULHSA-N 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021154677A JP2021193138A (ja) | 2016-10-05 | 2021-09-22 | スピロ環化合物 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662404668P | 2016-10-05 | 2016-10-05 | |
| US62/404,668 | 2016-10-05 | ||
| PCT/US2017/054865 WO2018067512A1 (en) | 2016-10-05 | 2017-10-03 | Spirocyclic compounds |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021154677A Division JP2021193138A (ja) | 2016-10-05 | 2021-09-22 | スピロ環化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019534261A JP2019534261A (ja) | 2019-11-28 |
| JP2019534261A5 true JP2019534261A5 (enExample) | 2020-11-12 |
| JP6949952B2 JP6949952B2 (ja) | 2021-10-13 |
Family
ID=61831517
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019518440A Expired - Fee Related JP6949952B2 (ja) | 2016-10-05 | 2017-10-03 | スピロ環化合物 |
| JP2021154677A Pending JP2021193138A (ja) | 2016-10-05 | 2021-09-22 | スピロ環化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021154677A Pending JP2021193138A (ja) | 2016-10-05 | 2021-09-22 | スピロ環化合物 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US10934304B2 (enExample) |
| EP (1) | EP3523306A4 (enExample) |
| JP (2) | JP6949952B2 (enExample) |
| KR (1) | KR20190075931A (enExample) |
| CN (1) | CN109890827A (enExample) |
| AU (1) | AU2017339890A1 (enExample) |
| BR (1) | BR112019005305A2 (enExample) |
| CA (1) | CA3037064A1 (enExample) |
| IL (1) | IL265752A (enExample) |
| MX (1) | MX2019003938A (enExample) |
| RU (1) | RU2019107667A (enExample) |
| TW (1) | TW201817732A (enExample) |
| WO (1) | WO2018067512A1 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS58514B1 (sr) | 2012-06-13 | 2019-04-30 | Incyte Holdings Corp | Supstituisana triciklična jedinjenja kao inhibitori fgfr |
| PH12015502383B1 (en) | 2013-04-19 | 2023-02-03 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| TWI712601B (zh) | 2015-02-20 | 2020-12-11 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| MX379622B (es) | 2015-04-03 | 2025-03-11 | Recurium Ip Holdings Llc | Compuestos espirociclicos |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| HRP20241288T1 (hr) | 2018-05-04 | 2024-12-06 | Incyte Corporation | Čvrsti oblici fgfr inhibitora i postupci za njihovu proizvodnju |
| AU2019262579B2 (en) | 2018-05-04 | 2024-09-12 | Incyte Corporation | Salts of an FGFR inhibitor |
| CN112654396B (zh) * | 2018-09-07 | 2025-07-01 | 默克专利股份公司 | 5-吗啉-4-基-吡唑并[4,3-b]吡啶衍生物 |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CA3157361A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| JP7832891B2 (ja) | 2019-12-04 | 2026-03-18 | インサイト・コーポレイション | Ｆｇｆｒ阻害剤の誘導体 |
| CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| CN110922421B (zh) * | 2019-12-17 | 2023-05-05 | 安徽英特美科技有限公司 | 一种n-甲基-1,2,5,6-四氢吡啶-4-硼酸频哪醇酯的合成方法 |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2022221170A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| CA3220155A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| US11939331B2 (en) | 2021-06-09 | 2024-03-26 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| AU2024374279A1 (en) * | 2023-10-31 | 2026-03-12 | C4 Therapeutics, Inc. | Compounds for the degradation of mutant braf |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA84930C2 (ru) | 2004-05-14 | 2008-12-10 | Вертекс Фармасьютикалс Инкорпорейтед | Пиррольные соединения как ингибиторы протеинкиназ erk, их синтез и соответствующие промежуточные соединения |
| KR101417136B1 (ko) * | 2005-12-13 | 2014-08-07 | 머크 샤프 앤드 돔 코포레이션 | Ｅｒｋ 억제제인 폴리사이클릭 인다졸 유도체 및 이를 포함하는 약제학적 조성물 |
| WO2008063609A2 (en) | 2006-11-17 | 2008-05-29 | Polyera Corporation | Diimide-based semiconductor materials and methods of preparing and using the same |
| CA2691417A1 (en) * | 2007-06-18 | 2008-12-24 | Schering Corporation | Heterocyclic compounds and use thereof as erk inhibitors |
| EP2318388A2 (en) | 2008-07-23 | 2011-05-11 | Schering Corporation | Tricyclic spirocycle derivatives and methods of use thereof |
| EP3296398A1 (en) | 2009-12-07 | 2018-03-21 | Arbutus Biopharma Corporation | Compositions for nucleic acid delivery |
| US8664213B2 (en) * | 2011-08-29 | 2014-03-04 | Bristol-Myers Squibb Company | Spiro bicyclic diamine derivatives as HIV attachment inhibitors |
| CN103130775B (zh) | 2011-11-22 | 2015-09-30 | 山东亨利医药科技有限责任公司 | 作为酪氨酸激酶抑制剂的吲哚满酮衍生物 |
| US8987264B2 (en) | 2012-11-09 | 2015-03-24 | Bristol-Myers Squibb Company | 1,3,5-triazine derivatives of spiro bicyclic oxalamide-compounds for treatment of hepatitis C |
| US9447026B2 (en) | 2013-03-14 | 2016-09-20 | Kalyra Pharmaceuticals, Inc. | Bicyclic analgesic compounds |
| US9879029B2 (en) | 2014-12-22 | 2018-01-30 | Eli Lilly And Company | ERK inhibitors |
| CN105732636B (zh) * | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | 杂芳化合物及其在药物中的应用 |
| MX379622B (es) | 2015-04-03 | 2025-03-11 | Recurium Ip Holdings Llc | Compuestos espirociclicos |
-
2017
- 2017-10-03 AU AU2017339890A patent/AU2017339890A1/en not_active Abandoned
- 2017-10-03 EP EP17858989.1A patent/EP3523306A4/en not_active Withdrawn
- 2017-10-03 CN CN201780067175.6A patent/CN109890827A/zh active Pending
- 2017-10-03 KR KR1020197012021A patent/KR20190075931A/ko not_active Ceased
- 2017-10-03 BR BR112019005305A patent/BR112019005305A2/pt not_active Application Discontinuation
- 2017-10-03 US US16/336,854 patent/US10934304B2/en not_active Expired - Fee Related
- 2017-10-03 MX MX2019003938A patent/MX2019003938A/es unknown
- 2017-10-03 JP JP2019518440A patent/JP6949952B2/ja not_active Expired - Fee Related
- 2017-10-03 RU RU2019107667A patent/RU2019107667A/ru not_active Application Discontinuation
- 2017-10-03 WO PCT/US2017/054865 patent/WO2018067512A1/en not_active Ceased
- 2017-10-03 CA CA3037064A patent/CA3037064A1/en not_active Abandoned
- 2017-10-05 TW TW106134299A patent/TW201817732A/zh unknown
-
2019
- 2019-04-01 IL IL265752A patent/IL265752A/en unknown
-
2020
- 2020-12-18 US US17/127,710 patent/US20210115058A1/en not_active Abandoned
-
2021
- 2021-09-22 JP JP2021154677A patent/JP2021193138A/ja active Pending
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