CN106535890A - 5‑取代的吲唑‑3‑羧酰胺及其制备和应用 - Google Patents
5‑取代的吲唑‑3‑羧酰胺及其制备和应用 Download PDFInfo
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- CN106535890A CN106535890A CN201580026082.XA CN201580026082A CN106535890A CN 106535890 A CN106535890 A CN 106535890A CN 201580026082 A CN201580026082 A CN 201580026082A CN 106535890 A CN106535890 A CN 106535890A
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- Prior art keywords
- pyridin
- carboxylic acid
- acid amides
- bases
- methyl
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- 0 C*(C)CCCNC Chemical compound C*(C)CCCNC 0.000 description 31
- OXHJXUOYSPSTOU-UHFFFAOYSA-N CC(C)CN(C1)CC1NC(C(C1C2)=NNC1=C=C=C2c1cncc(F)c1)=O Chemical compound CC(C)CN(C1)CC1NC(C(C1C2)=NNC1=C=C=C2c1cncc(F)c1)=O OXHJXUOYSPSTOU-UHFFFAOYSA-N 0.000 description 1
- IPBVMBFTMMTZPK-UHFFFAOYSA-N CC(C)CN(CC1)CCC1NC(c(c1c2)n[nH]c1ccc2-c(cccc1F)c1F)=O Chemical compound CC(C)CN(CC1)CCC1NC(c(c1c2)n[nH]c1ccc2-c(cccc1F)c1F)=O IPBVMBFTMMTZPK-UHFFFAOYSA-N 0.000 description 1
- ZTADWDFEENXOJJ-UHFFFAOYSA-N CC(C)NC(c1n[nH]c(cc2)c1cc2-c1cncc2c1cccc2)=O Chemical compound CC(C)NC(c1n[nH]c(cc2)c1cc2-c1cncc2c1cccc2)=O ZTADWDFEENXOJJ-UHFFFAOYSA-N 0.000 description 1
- QWXGMMPJHDIFKI-UHFFFAOYSA-N CC(C)Oc(nc1)ccc1NC(c(c1c2)n[nH]c1ccc2-c1cncc(CN2CCCCC2)c1)=O Chemical compound CC(C)Oc(nc1)ccc1NC(c(c1c2)n[nH]c1ccc2-c1cncc(CN2CCCCC2)c1)=O QWXGMMPJHDIFKI-UHFFFAOYSA-N 0.000 description 1
- XYLMBLGUIHNROA-OGSNPNQZSA-N CC/C(/c(cc1)cc2c1[nH]nc2C(Nc(cc1)cnc1Oc(cccc1)c1F)=O)=C\C(\CN1CCCCC1)=C/N Chemical compound CC/C(/c(cc1)cc2c1[nH]nc2C(Nc(cc1)cnc1Oc(cccc1)c1F)=O)=C\C(\CN1CCCCC1)=C/N XYLMBLGUIHNROA-OGSNPNQZSA-N 0.000 description 1
- ATGLNCFOYSXHFN-UHFFFAOYSA-N CN(C1)CC1(CC1)CCC1NC(c1n[nH]c(cc2)c1cc2-c1cncc(F)c1)=O Chemical compound CN(C1)CC1(CC1)CCC1NC(c1n[nH]c(cc2)c1cc2-c1cncc(F)c1)=O ATGLNCFOYSXHFN-UHFFFAOYSA-N 0.000 description 1
- YIPUNAJVDQWMHW-UHFFFAOYSA-N Cc1c(C(NCCN2CCOCC2)=O)c2cc(C3=CC=CNC3)ccc2[nH]1 Chemical compound Cc1c(C(NCCN2CCOCC2)=O)c2cc(C3=CC=CNC3)ccc2[nH]1 YIPUNAJVDQWMHW-UHFFFAOYSA-N 0.000 description 1
- LFBFXALMTINNJN-UHFFFAOYSA-N Clc1cncc(-c(cc2)cc3c2[nH]nc3C(NC2CCCC2)=[U])c1 Chemical compound Clc1cncc(-c(cc2)cc3c2[nH]nc3C(NC2CCCC2)=[U])c1 LFBFXALMTINNJN-UHFFFAOYSA-N 0.000 description 1
- DSIBUAUKJAXSDG-UHFFFAOYSA-N FC(CN(CC1)CCC1NC(c(c1c2)n[nH]c1ccc2-c1cnccc1)=[U])F Chemical compound FC(CN(CC1)CCC1NC(c(c1c2)n[nH]c1ccc2-c1cnccc1)=[U])F DSIBUAUKJAXSDG-UHFFFAOYSA-N 0.000 description 1
- ZBSQRSAMKYIVHH-UHFFFAOYSA-N Nc1cc(N2CCCC2)ncc1 Chemical compound Nc1cc(N2CCCC2)ncc1 ZBSQRSAMKYIVHH-UHFFFAOYSA-N 0.000 description 1
- NUABVQASABNFKF-UHFFFAOYSA-N O=C(c(c1c2)n[nH]c1ccc2-c1cncc(CN2CCCCC2)c1)NC1C=NC(C(F)(F)F)=NC1 Chemical compound O=C(c(c1c2)n[nH]c1ccc2-c1cncc(CN2CCCCC2)c1)NC1C=NC(C(F)(F)F)=NC1 NUABVQASABNFKF-UHFFFAOYSA-N 0.000 description 1
- MUJCJYXCJZCTGK-DIAVIDTQSA-N O=C(c(c1c2)n[nH]c1ccc2-c1cnccc1)NC(C1)[C@H]1c1ccccc1 Chemical compound O=C(c(c1c2)n[nH]c1ccc2-c1cnccc1)NC(C1)[C@H]1c1ccccc1 MUJCJYXCJZCTGK-DIAVIDTQSA-N 0.000 description 1
- CUPLUWNGXPNDOB-UHFFFAOYSA-N OCC(CO)(C1)CN1c(nc1)ccc1NC(c1n[nH]c(cc2)c1cc2C1=CC(CN2CCCCC2)CN=C1)=O Chemical compound OCC(CO)(C1)CN1c(nc1)ccc1NC(c1n[nH]c(cc2)c1cc2C1=CC(CN2CCCCC2)CN=C1)=O CUPLUWNGXPNDOB-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- 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
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- C07B59/002—Heterocyclic compounds
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- 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
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- 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
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- C07D498/08—Bridged systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Dermatology (AREA)
- Psychology (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
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- Child & Adolescent Psychology (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461968350P | 2014-03-20 | 2014-03-20 | |
| US61/968,350 | 2014-03-20 | ||
| PCT/US2015/021847 WO2015143380A1 (en) | 2014-03-20 | 2015-03-20 | 5-substituted indazole-3-carboxamides and preparation and use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106535890A true CN106535890A (zh) | 2017-03-22 |
Family
ID=54141450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201580026082.XA Pending CN106535890A (zh) | 2014-03-20 | 2015-03-20 | 5‑取代的吲唑‑3‑羧酰胺及其制备和应用 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US9745271B2 (https=) |
| EP (1) | EP3119393A4 (https=) |
| JP (1) | JP6586104B2 (https=) |
| KR (1) | KR20160135283A (https=) |
| CN (1) | CN106535890A (https=) |
| BR (1) | BR112016021626A2 (https=) |
| CA (1) | CA2942687A1 (https=) |
| CL (1) | CL2016002364A1 (https=) |
| IL (1) | IL247713A0 (https=) |
| MA (1) | MA39763A (https=) |
| MX (1) | MX2016012208A (https=) |
| PE (1) | PE20170127A1 (https=) |
| PH (1) | PH12016501835A1 (https=) |
| RU (1) | RU2016141088A (https=) |
| SG (2) | SG11201607816UA (https=) |
| WO (1) | WO2015143380A1 (https=) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112020501A (zh) * | 2018-02-23 | 2020-12-01 | 萨穆梅德有限公司 | 5-杂芳基取代的吲唑-3-基甲酰胺类及其制备和用途 |
| CN112135821A (zh) * | 2018-05-07 | 2020-12-25 | 方济各安吉利克化学联合股份有限公司 | 作为糖原合酶激酶3β抑制剂的1H-吲唑-3-甲酰胺化合物 |
| CN113735798A (zh) * | 2021-09-27 | 2021-12-03 | 安徽美致诚药业有限公司 | 一种盐酸罗沙替丁醋酸酯的制备方法 |
| WO2022052861A1 (zh) * | 2020-09-09 | 2022-03-17 | 成都奥睿药业有限公司 | 5-取代吲哚3-酰胺衍生物及其制备方法和用途 |
| CN114867718A (zh) * | 2019-12-16 | 2022-08-05 | 韩国化学研究院 | 新型吲唑衍生物及其用途 |
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| CN114867718A (zh) * | 2019-12-16 | 2022-08-05 | 韩国化学研究院 | 新型吲唑衍生物及其用途 |
| CN114867718B (zh) * | 2019-12-16 | 2024-10-01 | 韩国化学研究院 | 新型吲唑衍生物及其用途 |
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| US20180127377A1 (en) | 2018-05-10 |
| WO2015143380A1 (en) | 2015-09-24 |
| BR112016021626A2 (pt) | 2018-05-15 |
| EP3119393A4 (en) | 2018-02-28 |
| EP3119393A1 (en) | 2017-01-25 |
| KR20160135283A (ko) | 2016-11-25 |
| US20150266825A1 (en) | 2015-09-24 |
| US9745271B2 (en) | 2017-08-29 |
| SG11201607816UA (en) | 2016-10-28 |
| US10669240B2 (en) | 2020-06-02 |
| MX2016012208A (es) | 2017-01-26 |
| JP6586104B2 (ja) | 2019-10-02 |
| CL2016002364A1 (es) | 2017-06-23 |
| PE20170127A1 (es) | 2017-03-30 |
| RU2016141088A (ru) | 2018-04-25 |
| PH12016501835A1 (en) | 2017-01-09 |
| RU2016141088A3 (https=) | 2018-11-20 |
| IL247713A0 (en) | 2016-11-30 |
| JP2017508763A (ja) | 2017-03-30 |
| MA39763A (fr) | 2017-01-25 |
| CA2942687A1 (en) | 2015-09-24 |
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Application publication date: 20170322 |