KR20170005861A - 항당뇨병 트리시클릭 화합물 - Google Patents
항당뇨병 트리시클릭 화합물 Download PDFInfo
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- KR20170005861A KR20170005861A KR1020167035452A KR20167035452A KR20170005861A KR 20170005861 A KR20170005861 A KR 20170005861A KR 1020167035452 A KR1020167035452 A KR 1020167035452A KR 20167035452 A KR20167035452 A KR 20167035452A KR 20170005861 A KR20170005861 A KR 20170005861A
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- alkyl
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- 0 *C1C2(*)C3=C*CCC=[U]*=C3C(*)(*)C12 Chemical compound *C1C2(*)C3=C*CCC=[U]*=C3C(*)(*)C12 0.000 description 4
- YULMNMJFAZWLLN-UHFFFAOYSA-N C=C1CCCCC1 Chemical compound C=C1CCCCC1 YULMNMJFAZWLLN-UHFFFAOYSA-N 0.000 description 1
- KUGXJBUNFYDCOR-ZHKQWDMFSA-N CC(C)(C)OC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc(cc([C@@H](CC1N(C)C)C2C=CC=CC2(C)C(F)(F)F)c1c1)c1F)=O Chemical compound CC(C)(C)OC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc(cc([C@@H](CC1N(C)C)C2C=CC=CC2(C)C(F)(F)F)c1c1)c1F)=O KUGXJBUNFYDCOR-ZHKQWDMFSA-N 0.000 description 1
- ZBYUOQNWTLONQL-FQNJNTOFSA-N CC(C)(C)OC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc1cc([n](Cc2c(C(F)(F)F)cccc2)cc2)c2cc1F)=O Chemical compound CC(C)(C)OC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc1cc([n](Cc2c(C(F)(F)F)cccc2)cc2)c2cc1F)=O ZBYUOQNWTLONQL-FQNJNTOFSA-N 0.000 description 1
- JTABZYBBJOMLFD-UHFFFAOYSA-N CC(C)(CC(O)=O)c(cc1Br)ccc1F Chemical compound CC(C)(CC(O)=O)c(cc1Br)ccc1F JTABZYBBJOMLFD-UHFFFAOYSA-N 0.000 description 1
- LSKBTOWHXVGDAG-WVQWTBLQSA-N CC(C)(CC1)c(ccc(COC2=C[IH]C=C([C@@H]([C@H]3C4)[C@H]3C(O)=O)C4=C2)c2F)c2N1c1ccccc1C(F)(F)F Chemical compound CC(C)(CC1)c(ccc(COC2=C[IH]C=C([C@@H]([C@H]3C4)[C@H]3C(O)=O)C4=C2)c2F)c2N1c1ccccc1C(F)(F)F LSKBTOWHXVGDAG-WVQWTBLQSA-N 0.000 description 1
- QHUNHFMFBPDBLU-KXNZWBDNSA-N CC(C)(CC1c2c(C(F)(F)F)cccc2)c2c1cc(COc1ncc([C@@H]([C@H]3C4)[C@H]3C(O)=O)c4c1)cc2 Chemical compound CC(C)(CC1c2c(C(F)(F)F)cccc2)c2c1cc(COc1ncc([C@@H]([C@H]3C4)[C@H]3C(O)=O)c4c1)cc2 QHUNHFMFBPDBLU-KXNZWBDNSA-N 0.000 description 1
- RLMINEBEFJOFRZ-UHFFFAOYSA-N CC(C)(CNC1c2ccccc2C(F)(F)F)c2c1c(F)c(CBr)cc2 Chemical compound CC(C)(CNC1c2ccccc2C(F)(F)F)c2c1c(F)c(CBr)cc2 RLMINEBEFJOFRZ-UHFFFAOYSA-N 0.000 description 1
- SGYZQJSKGPLNNE-BQFBPARGSA-N CC(C)(OC1)OCC1(C1)c2ccc(COC3=NCC([C@H]([C@H]4C(O)=O)C4=C4)C4=C3)cc2C1c1c(C(F)(F)F)cccc1 Chemical compound CC(C)(OC1)OCC1(C1)c2ccc(COC3=NCC([C@H]([C@H]4C(O)=O)C4=C4)C4=C3)cc2C1c1c(C(F)(F)F)cccc1 SGYZQJSKGPLNNE-BQFBPARGSA-N 0.000 description 1
- OTNMIPUOVRLFAK-UHFFFAOYSA-N CCOC(C(C(C)(C)c(cc1Br)ccc1F)C#N)=O Chemical compound CCOC(C(C(C)(C)c(cc1Br)ccc1F)C#N)=O OTNMIPUOVRLFAK-UHFFFAOYSA-N 0.000 description 1
- NNGPFXVOEQHKCV-MIJFFNJWSA-N CCOC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc(cc(C(c1ccccc1C(F)(F)F)N(CC1(C)C)C(OC(C)(C)C)=O)c1c1)c1F)=O Chemical compound CCOC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc(cc(C(c1ccccc1C(F)(F)F)N(CC1(C)C)C(OC(C)(C)C)=O)c1c1)c1F)=O NNGPFXVOEQHKCV-MIJFFNJWSA-N 0.000 description 1
- KGIBUNRTPMIHAE-RJICFPRKSA-N CCOC([C@@H]([C@@H]1Cc2c3)[C@H]1c2cnc3OCc(cc(C(Cc1ccccc1C(F)(F)F)N(CC1(C)C)C(OC(C)(C)C)=O)c1c1)c1F)=O Chemical compound CCOC([C@@H]([C@@H]1Cc2c3)[C@H]1c2cnc3OCc(cc(C(Cc1ccccc1C(F)(F)F)N(CC1(C)C)C(OC(C)(C)C)=O)c1c1)c1F)=O KGIBUNRTPMIHAE-RJICFPRKSA-N 0.000 description 1
- HBNSUTKNYIPLLW-UHFFFAOYSA-N CCOC(c(cc(C(CC1=O)c2ccccc2C(F)(F)F)c1c1)c1F)=O Chemical compound CCOC(c(cc(C(CC1=O)c2ccccc2C(F)(F)F)c1c1)c1F)=O HBNSUTKNYIPLLW-UHFFFAOYSA-N 0.000 description 1
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- SUYNNKFECKOSDE-UHFFFAOYSA-N CCOC(c(ccc1c2C(c3c(C(F)(F)F)cccc3)=NCC1(C)C)c2F)=O Chemical compound CCOC(c(ccc1c2C(c3c(C(F)(F)F)cccc3)=NCC1(C)C)c2F)=O SUYNNKFECKOSDE-UHFFFAOYSA-N 0.000 description 1
- HRRQDCXJSUQFNB-UHFFFAOYSA-N CCOC(c1cc(C(c2ccccc2C(F)(F)F)=NCC2(C)C)c2cc1F)=O Chemical compound CCOC(c1cc(C(c2ccccc2C(F)(F)F)=NCC2(C)C)c2cc1F)=O HRRQDCXJSUQFNB-UHFFFAOYSA-N 0.000 description 1
- RGIZDZXUWUKCDC-UHFFFAOYSA-N CCOC(c1ccc(C(C)(C)CC2=O)c2c1)=O Chemical compound CCOC(c1ccc(C(C)(C)CC2=O)c2c1)=O RGIZDZXUWUKCDC-UHFFFAOYSA-N 0.000 description 1
- BAKLBGDXZNTXSJ-UHFFFAOYSA-N CCOC(c1ccc(C(C)(C)CNC(c2c(C(F)(F)F)cccc2)=O)cc1F)=O Chemical compound CCOC(c1ccc(C(C)(C)CNC(c2c(C(F)(F)F)cccc2)=O)cc1F)=O BAKLBGDXZNTXSJ-UHFFFAOYSA-N 0.000 description 1
- LVVKREHDHBJXTI-UHFFFAOYSA-N Nc(cc1)cc(C(F)(F)F)c1-[n]1ncc(cc2F)c1cc2Br Chemical compound Nc(cc1)cc(C(F)(F)F)c1-[n]1ncc(cc2F)c1cc2Br LVVKREHDHBJXTI-UHFFFAOYSA-N 0.000 description 1
- RMJORVCOJCYPCG-QFWMQHCXSA-N OC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc(cc1)cc2c1OCCN2c1ccccc1)=O Chemical compound OC([C@@H]([C@@H]1C2)[C@H]1c(cn1)c2cc1OCc(cc1)cc2c1OCCN2c1ccccc1)=O RMJORVCOJCYPCG-QFWMQHCXSA-N 0.000 description 1
- FCVLCBZLNVLZKI-ISZHWKRNSA-N OC([C@@H]([C@@H]1Cc2c3)[C@H]1c2cnc3OCc1ccc(C(CC2c3c(C(F)(F)F)cccc3)c3ccccc3)c2c1)=O Chemical compound OC([C@@H]([C@@H]1Cc2c3)[C@H]1c2cnc3OCc1ccc(C(CC2c3c(C(F)(F)F)cccc3)c3ccccc3)c2c1)=O FCVLCBZLNVLZKI-ISZHWKRNSA-N 0.000 description 1
- NNNALTDIIRCPKD-ZMCJUPGHSA-N OC([C@@](C1)(C2)[C@@H]1Cc1c2cnc(OCc2ccc(C3(COC3)CC3c4ccccc4C(F)(F)F)c3c2)c1)=O Chemical compound OC([C@@](C1)(C2)[C@@H]1Cc1c2cnc(OCc2ccc(C3(COC3)CC3c4ccccc4C(F)(F)F)c3c2)c1)=O NNNALTDIIRCPKD-ZMCJUPGHSA-N 0.000 description 1
- YJJMXGWNAMHBSJ-UHFFFAOYSA-N OCc1cc([n](Cc2c(C(F)(F)F)cccc2)cc2)c2cc1F Chemical compound OCc1cc([n](Cc2c(C(F)(F)F)cccc2)cc2)c2cc1F YJJMXGWNAMHBSJ-UHFFFAOYSA-N 0.000 description 1
- VNLOUSYIWHGZEJ-UHFFFAOYSA-N [O-][N+](c(cc1)cc(C(F)(F)F)c1-[n]1ncc(cc2F)c1cc2Br)=O Chemical compound [O-][N+](c(cc1)cc(C(F)(F)F)c1-[n]1ncc(cc2F)c1cc2Br)=O VNLOUSYIWHGZEJ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/16—Ring systems of three rings containing carbocyclic rings other than six-membered
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
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- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
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- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
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- C07C61/39—Unsaturated compounds containing six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—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
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- C07D215/14—Radicals substituted by oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- 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
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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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- 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
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- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
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- Y10S514/866—
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- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2014/078104 WO2015176267A1 (en) | 2014-05-22 | 2014-05-22 | Antidiabetic tricyclic compounds |
| CNPCT/CN2014/078104 | 2014-05-22 | ||
| PCT/CN2015/079262 WO2015176640A1 (en) | 2014-05-22 | 2015-05-19 | Antidiabetic tricyclic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20170005861A true KR20170005861A (ko) | 2017-01-16 |
Family
ID=54553222
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| KR1020167035452A Withdrawn KR20170005861A (ko) | 2014-05-22 | 2015-05-19 | 항당뇨병 트리시클릭 화합물 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10000454B2 (OSRAM) |
| EP (1) | EP3145915B1 (OSRAM) |
| JP (1) | JP2017516771A (OSRAM) |
| KR (1) | KR20170005861A (OSRAM) |
| CN (1) | CN106458913A (OSRAM) |
| AU (1) | AU2015263620B2 (OSRAM) |
| CA (1) | CA2947781A1 (OSRAM) |
| ES (1) | ES3016636T3 (OSRAM) |
| MX (1) | MX2016015182A (OSRAM) |
| RU (1) | RU2016150413A (OSRAM) |
| WO (2) | WO2015176267A1 (OSRAM) |
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| CN106588673B (zh) * | 2016-12-20 | 2018-06-26 | 金凯(辽宁)化工有限公司 | 一种2-甲基-5-氨基三氟甲苯的制备方法 |
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| CN111712494A (zh) | 2018-02-13 | 2020-09-25 | 吉利德科学公司 | Pd-1/pd-l1抑制剂 |
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| CA3101832A1 (en) | 2018-05-31 | 2019-12-05 | Hua Medicine (Shanghai) Ltd. | Pharmaceutical combination, composition and formulation containing glucokinase activator and a-glucosidase inhibitor, preparation methods and uses thereof |
| KR20230159715A (ko) | 2018-07-13 | 2023-11-21 | 길리애드 사이언시즈, 인코포레이티드 | Pd-1/pd-l1 억제제 |
| US11590161B2 (en) | 2018-08-13 | 2023-02-28 | Viscera Labs, Inc. | Therapeutic composition and methods |
| US11524029B2 (en) | 2018-08-13 | 2022-12-13 | Viscera Labs, Inc. | Therapeutic composition and methods |
| AU2019366355B2 (en) | 2018-10-24 | 2022-10-13 | Gilead Sciences, Inc. | PD-1/PD-L1 inhibitors |
| CN116159052B (zh) * | 2019-03-18 | 2025-04-11 | 深圳微芯生物科技股份有限公司 | 联合用药应用以及一种药用组合物及其应用 |
| CN112574122B (zh) * | 2019-09-27 | 2024-05-31 | 上海天慈国际药业有限公司 | 一种奥拉帕尼关键中间体的制备方法 |
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| BR112022017039A2 (pt) | 2020-02-28 | 2022-11-16 | Kallyope Inc | Agonistas de gpr40 |
| JP2023526625A (ja) | 2020-05-19 | 2023-06-22 | キャリーオペ,インク. | Ampkアクチベーター |
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| CN114249724B (zh) * | 2020-09-25 | 2023-05-26 | 鲁南制药集团股份有限公司 | 一种唑吡坦中间体的制备方法 |
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-
2014
- 2014-05-22 WO PCT/CN2014/078104 patent/WO2015176267A1/en not_active Ceased
-
2015
- 2015-05-19 CA CA2947781A patent/CA2947781A1/en not_active Abandoned
- 2015-05-19 ES ES15795833T patent/ES3016636T3/es active Active
- 2015-05-19 WO PCT/CN2015/079262 patent/WO2015176640A1/en not_active Ceased
- 2015-05-19 EP EP15795833.1A patent/EP3145915B1/en active Active
- 2015-05-19 CN CN201580026394.0A patent/CN106458913A/zh active Pending
- 2015-05-19 US US15/310,488 patent/US10000454B2/en active Active
- 2015-05-19 AU AU2015263620A patent/AU2015263620B2/en not_active Ceased
- 2015-05-19 JP JP2016568635A patent/JP2017516771A/ja active Pending
- 2015-05-19 RU RU2016150413A patent/RU2016150413A/ru not_active Application Discontinuation
- 2015-05-19 MX MX2016015182A patent/MX2016015182A/es unknown
- 2015-05-19 KR KR1020167035452A patent/KR20170005861A/ko not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CA2947781A1 (en) | 2015-11-26 |
| RU2016150413A3 (OSRAM) | 2018-11-16 |
| RU2016150413A (ru) | 2018-06-26 |
| EP3145915A4 (en) | 2017-11-01 |
| EP3145915B1 (en) | 2025-03-19 |
| WO2015176267A1 (en) | 2015-11-26 |
| AU2015263620B2 (en) | 2019-02-07 |
| WO2015176640A1 (en) | 2015-11-26 |
| AU2015263620A8 (en) | 2017-02-02 |
| US20170081287A1 (en) | 2017-03-23 |
| AU2015263620A1 (en) | 2016-10-20 |
| MX2016015182A (es) | 2017-03-03 |
| US10000454B2 (en) | 2018-06-19 |
| EP3145915A1 (en) | 2017-03-29 |
| JP2017516771A (ja) | 2017-06-22 |
| ES3016636T3 (en) | 2025-05-09 |
| CN106458913A (zh) | 2017-02-22 |
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