AU2008241692B2 - DPP-IV inhibitor including beta-amino group, preparation method thereof and pharmaceutical composition containing the same for preventing and treating a diabetes or an obesity - Google Patents
DPP-IV inhibitor including beta-amino group, preparation method thereof and pharmaceutical composition containing the same for preventing and treating a diabetes or an obesity Download PDFInfo
- Publication number
- AU2008241692B2 AU2008241692B2 AU2008241692A AU2008241692A AU2008241692B2 AU 2008241692 B2 AU2008241692 B2 AU 2008241692B2 AU 2008241692 A AU2008241692 A AU 2008241692A AU 2008241692 A AU2008241692 A AU 2008241692A AU 2008241692 B2 AU2008241692 B2 AU 2008241692B2
- Authority
- AU
- Australia
- Prior art keywords
- amino
- piperazin
- trifluorophenyl
- butanoyl
- compound
- 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.)
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- 238000002360 preparation method Methods 0.000 title claims description 35
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 18
- 206010012601 diabetes mellitus Diseases 0.000 title claims description 15
- 208000008589 Obesity Diseases 0.000 title claims description 13
- 235000020824 obesity Nutrition 0.000 title claims description 13
- 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 title description 67
- 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 title description 67
- 239000003112 inhibitor Substances 0.000 title description 18
- 150000001875 compounds Chemical class 0.000 claims description 153
- 150000003839 salts Chemical class 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 22
- -1 tert-butylthio Chemical group 0.000 claims description 15
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 claims description 14
- 238000011282 treatment Methods 0.000 claims description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 13
- 239000004480 active ingredient Substances 0.000 claims description 13
- 239000003814 drug Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
- 239000012453 solvate Substances 0.000 claims description 8
- 230000002265 prevention Effects 0.000 claims description 7
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 6
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 claims description 5
- LCDDAGSJHKEABN-MLGOLLRUSA-N Evogliptin Chemical compound C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F LCDDAGSJHKEABN-MLGOLLRUSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 229940049920 malate Drugs 0.000 claims description 4
- ARRSMTOBGAEBNU-BWTUWSSMSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(methoxymethyl)piperazin-2-one;hydrochloride Chemical compound Cl.C1CNC(=O)[C@@H](COC)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F ARRSMTOBGAEBNU-BWTUWSSMSA-N 0.000 claims description 3
- ACHKJXIEWPVFMN-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(propan-2-yloxymethyl)piperazin-2-one;hydrochloride Chemical compound Cl.C1CNC(=O)[C@@H](COC(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F ACHKJXIEWPVFMN-VQZRABBESA-N 0.000 claims description 3
- OOIZCGTVXPRMED-KKJWGQAZSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(tert-butylsulfanylmethyl)piperazin-2-one;hydrochloride Chemical compound Cl.C1CNC(=O)[C@H](CSC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F OOIZCGTVXPRMED-KKJWGQAZSA-N 0.000 claims description 3
- RBBXDAJRSNHIJZ-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)C(O)C(O)C(O)=O.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F RBBXDAJRSNHIJZ-VQZRABBESA-N 0.000 claims description 3
- MXGQQJCNCWYMHY-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one;butanedioic acid Chemical compound OC(=O)CCC(O)=O.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F MXGQQJCNCWYMHY-VQZRABBESA-N 0.000 claims description 3
- QHQXWMKKQNSBTC-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one;hydrochloride Chemical compound Cl.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F QHQXWMKKQNSBTC-VQZRABBESA-N 0.000 claims description 3
- XTHKWIKZDKDZOZ-BWDBLHBDSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[[ethyl(methyl)amino]methyl]piperazin-2-one;dihydrochloride Chemical compound Cl.Cl.C1CNC(=O)[C@@H](CN(C)CC)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F XTHKWIKZDKDZOZ-BWDBLHBDSA-N 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- ICEMCUCTLWJVRT-ZIAGYGMSSA-N (3r)-3-amino-1-[(2r)-2-[(2-methylpropan-2-yl)oxymethyl]piperazin-1-yl]-4-(2,4,5-trifluorophenyl)butan-1-one Chemical compound CC(C)(C)OC[C@H]1CNCCN1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F ICEMCUCTLWJVRT-ZIAGYGMSSA-N 0.000 claims description 2
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- UCHZSEWTMHMOTL-IAQYHMDHSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(ethoxymethyl)piperazin-2-one Chemical compound C1CNC(=O)[C@@H](COCC)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F UCHZSEWTMHMOTL-IAQYHMDHSA-N 0.000 claims description 2
- AOPBAUCNNSNYLA-OJYPLKCUSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(morpholin-4-ylmethyl)piperazin-2-one;dihydrochloride Chemical compound Cl.Cl.C([C@@H]1C(=O)NCCN1C(=O)C[C@H](N)CC=1C(=CC(F)=C(F)C=1)F)N1CCOCC1 AOPBAUCNNSNYLA-OJYPLKCUSA-N 0.000 claims description 2
- QTOODYCFKSZLPB-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F QTOODYCFKSZLPB-VQZRABBESA-N 0.000 claims description 2
- XZLNPSGPUSDWQD-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one;hexanedioic acid Chemical compound OC(=O)CCCCC(O)=O.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F XZLNPSGPUSDWQD-VQZRABBESA-N 0.000 claims description 2
- 241000124008 Mammalia Species 0.000 claims description 2
- ICEMCUCTLWJVRT-KGLIPLIRSA-N N[C@@H](CC(=O)N1[C@@H](CNCC1)COC(C)(C)C)CC1=C(C=C(C(=C1)F)F)F Chemical compound N[C@@H](CC(=O)N1[C@@H](CNCC1)COC(C)(C)C)CC1=C(C=C(C(=C1)F)F)F ICEMCUCTLWJVRT-KGLIPLIRSA-N 0.000 claims description 2
- TWOAUKUMWHDKDQ-VQZRABBESA-N acetic acid;(3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one Chemical compound CC(O)=O.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F TWOAUKUMWHDKDQ-VQZRABBESA-N 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
- C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Diabetes (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Hematology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Obesity (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20070038462 | 2007-04-19 | ||
| KR10-2007-0038462 | 2007-04-19 | ||
| PCT/KR2008/002203 WO2008130151A1 (en) | 2007-04-19 | 2008-04-18 | Dpp-iv inhibitor including beta-amino group, preparation method thereof and pharmaceutical composition containing the same for preventing and treating a diabetes or an obesity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2008241692A1 AU2008241692A1 (en) | 2008-10-30 |
| AU2008241692B2 true AU2008241692B2 (en) | 2011-02-10 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2008241692A Active AU2008241692B2 (en) | 2007-04-19 | 2008-04-18 | DPP-IV inhibitor including beta-amino group, preparation method thereof and pharmaceutical composition containing the same for preventing and treating a diabetes or an obesity |
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|---|---|
| US (1) | US8030315B2 (enExample) |
| EP (1) | EP2142519B1 (enExample) |
| JP (1) | JP5148686B2 (enExample) |
| KR (1) | KR101007497B1 (enExample) |
| CN (2) | CN101663282B (enExample) |
| AU (1) | AU2008241692B2 (enExample) |
| BR (1) | BRPI0810246B1 (enExample) |
| CA (1) | CA2683696C (enExample) |
| ES (1) | ES2526338T3 (enExample) |
| IL (1) | IL201524A (enExample) |
| MX (1) | MX2009011276A (enExample) |
| NZ (1) | NZ580701A (enExample) |
| PT (1) | PT2142519E (enExample) |
| RU (1) | RU2419615C1 (enExample) |
| WO (1) | WO2008130151A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101054911B1 (ko) * | 2008-10-17 | 2011-08-05 | 동아제약주식회사 | 디펩티딜펩티다아제-ⅳ의 활성을 저해하는 화합물 및 다른 항당뇨 또는 항비만 약물을 유효성분으로 함유하는 당뇨 또는 비만의 예방 및 치료용 약학적 조성물 |
| CN102378751B (zh) * | 2009-03-30 | 2014-08-20 | 东亚St株式会社 | 用于制备二肽基肽酶-iv抑制剂和中间体的改进方法 |
| SG174973A1 (en) * | 2009-03-30 | 2011-11-28 | Dong A Pharm Co Ltd | Improved method for manufacturing dipeptidyl peptidase-iv inhibitor and intermediate |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| KR20110107287A (ko) * | 2010-03-24 | 2011-09-30 | 동아제약주식회사 | 비알콜성 지방간 질환의 예방 및 치료용 약학적 조성물 |
| KR101180174B1 (ko) | 2010-04-23 | 2012-09-05 | 동아제약주식회사 | 신규한 벤즈아미드 유도체 |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| KR101290029B1 (ko) | 2011-01-20 | 2013-07-30 | 에스티팜 주식회사 | 시타글립틴의 중간체 제조방법 |
| CN102321014A (zh) * | 2011-05-27 | 2012-01-18 | 沈阳亿灵医药科技有限公司 | 新型双苯基吡啶类衍生物 |
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| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
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| BR112015032410B8 (pt) * | 2013-06-26 | 2021-10-26 | Dong A St Co Ltd | Uso de uma composição farmacêutica compreendendo inibidores de dpp-iv no preparo de um medicamento para prevenção ou tratamento de doenças renais |
| EP3273981B1 (en) | 2015-03-24 | 2020-04-29 | INSERM - Institut National de la Santé et de la Recherche Médicale | Method and pharmaceutical composition for use in the treatment of diabetes |
| KR101709127B1 (ko) | 2015-06-16 | 2017-02-22 | 경동제약 주식회사 | Dpp-iv 억제제의 제조를 위한 신규 중간체, 이의 제조방법 및 이를 이용한 dpp-iv 억제제의 제조방법 |
| CN107382757A (zh) * | 2017-08-11 | 2017-11-24 | 苏州信恩医药科技有限公司 | 不对称烯丙基取代反应在依格列汀中间体合成中的应用 |
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| NZ580701A (en) | 2011-07-29 |
| PT2142519E (pt) | 2014-12-11 |
| CN102516184A (zh) | 2012-06-27 |
| BRPI0810246B1 (pt) | 2021-11-30 |
| US8030315B2 (en) | 2011-10-04 |
| AU2008241692A1 (en) | 2008-10-30 |
| WO2008130151A1 (en) | 2008-10-30 |
| BRPI0810246A2 (pt) | 2015-08-18 |
| HK1138272A1 (en) | 2010-08-20 |
| CA2683696C (en) | 2012-05-22 |
| HK1172613A1 (en) | 2013-04-26 |
| CN101663282A (zh) | 2010-03-03 |
| RU2419615C1 (ru) | 2011-05-27 |
| EP2142519A4 (en) | 2011-07-13 |
| JP2011500508A (ja) | 2011-01-06 |
| CN101663282B (zh) | 2012-02-15 |
| EP2142519A1 (en) | 2010-01-13 |
| US20100120790A1 (en) | 2010-05-13 |
| CA2683696A1 (en) | 2008-10-30 |
| IL201524A (en) | 2014-09-30 |
| MX2009011276A (es) | 2010-01-15 |
| JP5148686B2 (ja) | 2013-02-20 |
| EP2142519B1 (en) | 2014-09-24 |
| ES2526338T3 (es) | 2015-01-09 |
| IL201524A0 (en) | 2010-05-31 |
| KR20080094604A (ko) | 2008-10-23 |
| CN102516184B (zh) | 2015-03-25 |
| KR101007497B1 (ko) | 2011-01-12 |
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