JP6912039B2 - 置換ベンゾイミダゾール、それらの調製及び医薬品としてのそれらの使用 - Google Patents
置換ベンゾイミダゾール、それらの調製及び医薬品としてのそれらの使用 Download PDFInfo
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- JP6912039B2 JP6912039B2 JP2018506999A JP2018506999A JP6912039B2 JP 6912039 B2 JP6912039 B2 JP 6912039B2 JP 2018506999 A JP2018506999 A JP 2018506999A JP 2018506999 A JP2018506999 A JP 2018506999A JP 6912039 B2 JP6912039 B2 JP 6912039B2
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- 0 *c([n](*)c1c2*)nc1c(*)c(*)c2C(C(*)=C1*)=C(*)N(*)C1=O Chemical compound *c([n](*)c1c2*)nc1c(*)c(*)c2C(C(*)=C1*)=C(*)N(*)C1=O 0.000 description 4
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- LZNWLEPJPMWRAU-UHFFFAOYSA-N CC1=CC(c(cc2)cc(NCCOCC(F)(F)F)c2[N+]([O-])=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)cc(NCCOCC(F)(F)F)c2[N+]([O-])=O)=CN(C)C1=O LZNWLEPJPMWRAU-UHFFFAOYSA-N 0.000 description 2
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- PXZKFECAINECTN-UHFFFAOYSA-N CC(C)(CC(c(cc1)cc(NCCOC(F)(F)F)c1N)=CN1C)C1=O Chemical compound CC(C)(CC(c(cc1)cc(NCCOC(F)(F)F)c1N)=CN1C)C1=O PXZKFECAINECTN-UHFFFAOYSA-N 0.000 description 1
- XSEWRPXQLCGDQL-NTEUORMPSA-N CC(C)OC/C(/C)=N/c(cc(cc1)Br)c1[N+]([O-])=O Chemical compound CC(C)OC/C(/C)=N/c(cc(cc1)Br)c1[N+]([O-])=O XSEWRPXQLCGDQL-NTEUORMPSA-N 0.000 description 1
- RETZKOVMQQKTET-UHFFFAOYSA-N CC(C)OCCNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1N Chemical compound CC(C)OCCNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1N RETZKOVMQQKTET-UHFFFAOYSA-N 0.000 description 1
- XCYVXDCJCCRFQM-UHFFFAOYSA-N CC(C)OCCNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1[N+]([O-])=O Chemical compound CC(C)OCCNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1[N+]([O-])=O XCYVXDCJCCRFQM-UHFFFAOYSA-N 0.000 description 1
- PHCNFIFMPMPDQX-CQSZACIVSA-N CC(C)OC[C@@H](C)Nc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1[N+]([O-])=O Chemical compound CC(C)OC[C@@H](C)Nc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1[N+]([O-])=O PHCNFIFMPMPDQX-CQSZACIVSA-N 0.000 description 1
- CHZCPIPXCVHABA-UHFFFAOYSA-N CC1=CC(c(cc2)cc(NCCC(F)(F)F)c2[N+]([O-])=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)cc(NCCC(F)(F)F)c2[N+]([O-])=O)=CN(C)C1=O CHZCPIPXCVHABA-UHFFFAOYSA-N 0.000 description 1
- VAYRDQOBRYXFLR-UHFFFAOYSA-N CC1=CC(c(cc2)cc(NCCOC(F)(F)F)c2NC(C2CCOCC2)=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)cc(NCCOC(F)(F)F)c2NC(C2CCOCC2)=O)=CN(C)C1=O VAYRDQOBRYXFLR-UHFFFAOYSA-N 0.000 description 1
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- MGUONTZTOXWFRF-UHFFFAOYSA-N CC1=CC(c(cc2)cc3c2nc(C2CCCCC2)[n]3CCOC)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)cc3c2nc(C2CCCCC2)[n]3CCOC)=CN(C)C1=O MGUONTZTOXWFRF-UHFFFAOYSA-N 0.000 description 1
- MYXRAGJJJUOGSZ-UHFFFAOYSA-N CC1=CC(c(cc2NCCOC)ccc2N)=CN(C)C1=O Chemical compound CC1=CC(c(cc2NCCOC)ccc2N)=CN(C)C1=O MYXRAGJJJUOGSZ-UHFFFAOYSA-N 0.000 description 1
- IOPDSZLMUOSZHZ-UHFFFAOYSA-N CCOCCNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1N Chemical compound CCOCCNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1N IOPDSZLMUOSZHZ-UHFFFAOYSA-N 0.000 description 1
- ZFRDNEQQDDWQHJ-KRWDZBQOSA-N CCO[C@@H](C)C[n]1c(cc(cc2)C(C=C3C)=CN(C)C3=O)c2nc1C(CC1)CCC1(F)F Chemical compound CCO[C@@H](C)C[n]1c(cc(cc2)C(C=C3C)=CN(C)C3=O)c2nc1C(CC1)CCC1(F)F ZFRDNEQQDDWQHJ-KRWDZBQOSA-N 0.000 description 1
- KUBZLZAZMNELCG-MRVPVSSYSA-N CCO[C@H](C)CNc(cc(cc1)Br)c1N Chemical compound CCO[C@H](C)CNc(cc(cc1)Br)c1N KUBZLZAZMNELCG-MRVPVSSYSA-N 0.000 description 1
- QMWWEMLJYVJWOS-MRVPVSSYSA-N CCO[C@H](C)CNc(cc(cc1)Br)c1[N+]([O-])=O Chemical compound CCO[C@H](C)CNc(cc(cc1)Br)c1[N+]([O-])=O QMWWEMLJYVJWOS-MRVPVSSYSA-N 0.000 description 1
- BBUARUBIXANZIS-CYBMUJFWSA-N CCO[C@H](C)CNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1N Chemical compound CCO[C@H](C)CNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1N BBUARUBIXANZIS-CYBMUJFWSA-N 0.000 description 1
- OSBPHVXQBVVYMK-OAHLLOKOSA-N CCO[C@H](C)CNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1NC(C(C1)CC1(F)F)=O Chemical compound CCO[C@H](C)CNc(cc(cc1)C(C=C2C)=CN(C)C2=O)c1NC(C(C1)CC1(F)F)=O OSBPHVXQBVVYMK-OAHLLOKOSA-N 0.000 description 1
- WIZDANJNJRRRQZ-INIZCTEOSA-N C[C@@H](COC)[n]1c(cc(cc2)C(C=C3C)=CN(C)C3=O)c2nc1C(CC1)CCC1(F)F Chemical compound C[C@@H](COC)[n]1c(cc(cc2)C(C=C3C)=CN(C)C3=O)c2nc1C(CC1)CCC1(F)F WIZDANJNJRRRQZ-INIZCTEOSA-N 0.000 description 1
- RGFKQNCZZJVQFC-UHFFFAOYSA-N Cc([n](CCOC(F)(F)F)c1c2)nc1ccc2C(C=C1C)=CN(C)C1=O Chemical compound Cc([n](CCOC(F)(F)F)c1c2)nc1ccc2C(C=C1C)=CN(C)C1=O RGFKQNCZZJVQFC-UHFFFAOYSA-N 0.000 description 1
- ILYVDFJXCZLQOG-UHFFFAOYSA-N Cc1nc(ccc(Br)c2)c2[n]1CCOC(F)(F)F Chemical compound Cc1nc(ccc(Br)c2)c2[n]1CCOC(F)(F)F ILYVDFJXCZLQOG-UHFFFAOYSA-N 0.000 description 1
- VOJANFHOLSIPBC-UHFFFAOYSA-N FC(CC1)(CCC1c([nH]c1c2)nc1ccc2Br)F Chemical compound FC(CC1)(CCC1c([nH]c1c2)nc1ccc2Br)F VOJANFHOLSIPBC-UHFFFAOYSA-N 0.000 description 1
- GXZZKJRWIAZFFL-UHFFFAOYSA-N [O-][N+](c(ccc(Br)c1)c1NCCOCC(F)(F)F)=O Chemical compound [O-][N+](c(ccc(Br)c1)c1NCCOCC(F)(F)F)=O GXZZKJRWIAZFFL-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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
- C07D401/10—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 linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/14—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 three or more hetero rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Obesity (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562204178P | 2015-08-12 | 2015-08-12 | |
| US62/204,178 | 2015-08-12 | ||
| US201662358101P | 2016-07-04 | 2016-07-04 | |
| US62/358,101 | 2016-07-04 | ||
| PCT/CA2016/050952 WO2017024412A1 (en) | 2015-08-12 | 2016-08-12 | Substituted benzimidazoles, their preparation and their use as pharmaceuticals |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018522925A JP2018522925A (ja) | 2018-08-16 |
| JP2018522925A5 JP2018522925A5 (https=) | 2019-09-26 |
| JP6912039B2 true JP6912039B2 (ja) | 2021-07-28 |
Family
ID=57982882
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018506999A Active JP6912039B2 (ja) | 2015-08-12 | 2016-08-12 | 置換ベンゾイミダゾール、それらの調製及び医薬品としてのそれらの使用 |
Country Status (11)
| Country | Link |
|---|---|
| US (4) | US10703740B2 (https=) |
| EP (1) | EP3334719B1 (https=) |
| JP (1) | JP6912039B2 (https=) |
| KR (1) | KR102784592B1 (https=) |
| CN (2) | CN114605387A (https=) |
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| KR102784592B1 (ko) * | 2015-08-12 | 2025-03-19 | 에피제네틱스, 인크. | 치환된 벤즈이미다졸, 그의 제조법 및 제약으로서의 그의 용도 |
| GB201617627D0 (en) | 2016-10-18 | 2016-11-30 | Cellcentric Ltd | Pharmaceutical compounds |
| GB201617630D0 (en) | 2016-10-18 | 2016-11-30 | Cellcentric Ltd | Pharmaceutical compounds |
| JP7165501B2 (ja) * | 2017-03-15 | 2022-11-04 | 住友ファーマ株式会社 | 新規ベンズイミダゾール化合物からなる医薬 |
| WO2018207882A1 (ja) * | 2017-05-12 | 2018-11-15 | 武田薬品工業株式会社 | 複素環化合物 |
| GB201806320D0 (en) | 2018-04-18 | 2018-05-30 | Cellcentric Ltd | Process |
| WO2020093162A1 (en) * | 2018-11-07 | 2020-05-14 | Neomed Institute | Treatment of bet inhibitor-resistant cancers and other diseases responsive to dual bet and cbp/ep300 inhibition therapy |
| JP2022053557A (ja) * | 2019-02-08 | 2022-04-06 | マルホ株式会社 | ピリドン誘導体 |
| CN112174945B (zh) * | 2019-07-02 | 2022-06-07 | 四川大学 | 具有抗癌作用的吲唑类化合物及其制备方法和用途 |
| CN115232074A (zh) * | 2022-08-22 | 2022-10-25 | 湖南复瑞生物医药技术有限责任公司 | 一种1-烷基取代-2-甲基-5-溴苯并咪唑的合成方法 |
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| US20210107893A1 (en) | 2021-04-15 |
| KR20180039669A (ko) | 2018-04-18 |
| EP3334719B1 (en) | 2021-09-15 |
| CA2994478C (en) | 2023-10-03 |
| HK1256752A1 (en) | 2019-10-04 |
| US20180237417A1 (en) | 2018-08-23 |
| IL257340A (en) | 2018-03-29 |
| CN114605387A (zh) | 2022-06-10 |
| EP3334719A1 (en) | 2018-06-20 |
| CN108137539B (zh) | 2022-01-11 |
| US11365186B2 (en) | 2022-06-21 |
| EP3334719A4 (en) | 2019-02-06 |
| CA2994478A1 (en) | 2017-02-16 |
| US20240425481A1 (en) | 2024-12-26 |
| US20230120413A1 (en) | 2023-04-20 |
| US10703740B2 (en) | 2020-07-07 |
| IL257340B1 (en) | 2023-06-01 |
| BR112018002547A2 (pt) | 2018-09-18 |
| JP2018522925A (ja) | 2018-08-16 |
| ES2904258T3 (es) | 2022-04-04 |
| MX2018001756A (es) | 2018-09-06 |
| KR102784592B1 (ko) | 2025-03-19 |
| CN108137539A (zh) | 2018-06-08 |
| AU2021200147A1 (en) | 2021-03-18 |
| WO2017024412A1 (en) | 2017-02-16 |
| AU2016305515A1 (en) | 2018-03-08 |
| US11981657B2 (en) | 2024-05-14 |
| MX382832B (es) | 2025-03-13 |
| AU2021200147B2 (en) | 2022-09-08 |
| IL257340B2 (en) | 2023-10-01 |
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