JP2011500508A5 - - Google Patents
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- Publication number
- JP2011500508A5 JP2011500508A5 JP2010503979A JP2010503979A JP2011500508A5 JP 2011500508 A5 JP2011500508 A5 JP 2011500508A5 JP 2010503979 A JP2010503979 A JP 2010503979A JP 2010503979 A JP2010503979 A JP 2010503979A JP 2011500508 A5 JP2011500508 A5 JP 2011500508A5
- Authority
- JP
- Japan
- Prior art keywords
- amino
- butanoyl
- trifluorophenyl
- piperazin
- butoxymethyl
- 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
- 150000001875 compounds Chemical class 0.000 claims 17
- 239000000126 substance Substances 0.000 claims 8
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 claims 4
- 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 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 208000008589 Obesity Diseases 0.000 claims 3
- 206010012601 diabetes mellitus Diseases 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 235000020824 obesity Nutrition 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 239000012453 solvate Substances 0.000 claims 3
- AUPBGIVXZWXYCZ-VQZRABBESA-N (3R)-4-[(3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[[ethyl(methyl)amino]methyl]piperazin-2-one hydrochloride Chemical compound Cl.C1CNC(=O)[C@@H](CN(C)CC)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F AUPBGIVXZWXYCZ-VQZRABBESA-N 0.000 claims 2
- WCPBTTHTFYQGSW-QRGZVCNKSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(cyclopentyloxymethyl)piperazin-2-one;hydrochloride Chemical compound Cl.C([C@@H]1C(=O)NCCN1C(=O)C[C@H](N)CC=1C(=CC(F)=C(F)C=1)F)OC1CCCC1 WCPBTTHTFYQGSW-QRGZVCNKSA-N 0.000 claims 2
- PVLCCYCIVCNISH-OJYPLKCUSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(diethylaminomethyl)piperazin-2-one;dihydrochloride Chemical compound Cl.Cl.C1CNC(=O)[C@@H](CN(CC)CC)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F PVLCCYCIVCNISH-OJYPLKCUSA-N 0.000 claims 2
- ZSVLYYHXBXVIGU-GPKQSYPGSA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(ethoxymethyl)piperazin-2-one;hydrochloride Chemical compound Cl.C1CNC(=O)[C@@H](COCC)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F ZSVLYYHXBXVIGU-GPKQSYPGSA-N 0.000 claims 2
- 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 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 2
- 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 2
- 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 2
- 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 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 2
- 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 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 2
- 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 2
- YKEVRQCVHCQUBO-VQZRABBESA-N (3r)-4-[(3r)-3-amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-[(2-methylpropan-2-yl)oxymethyl]piperazin-2-one;phosphoric acid Chemical compound OP(O)(O)=O.C1CNC(=O)[C@@H](COC(C)(C)C)N1C(=O)C[C@H](N)CC1=CC(F)=C(F)C=C1F YKEVRQCVHCQUBO-VQZRABBESA-N 0.000 claims 2
- QHQXWMKKQNSBTC-KKJWGQAZSA-N (3s)-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-KKJWGQAZSA-N 0.000 claims 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 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229940049920 malate Drugs 0.000 claims 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- -1 tert-butoxy, methoxy, ethoxy, isopropoxy, cyclopentyloxy, diethylamino, ethylmethylamino, morpholino Chemical group 0.000 claims 2
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 230000003449 preventive effect Effects 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 150000001420 substituted heterocyclic compounds Chemical class 0.000 claims 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR10-2007-0038462 | 2007-04-19 | ||
| KR20070038462 | 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 (3)
| Publication Number | Publication Date |
|---|---|
| JP2011500508A JP2011500508A (ja) | 2011-01-06 |
| JP2011500508A5 true JP2011500508A5 (enExample) | 2011-07-21 |
| JP5148686B2 JP5148686B2 (ja) | 2013-02-20 |
Family
ID=39875638
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010503979A Active JP5148686B2 (ja) | 2007-04-19 | 2008-04-18 | β−アミノ基を含むＤＰＰ−ＩＶ阻害剤、その製造方法及びそれを有効成分として含む糖尿または肥満予防及び治療用医薬組成物 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8030315B2 (enExample) |
| EP (1) | EP2142519B1 (enExample) |
| JP (1) | JP5148686B2 (enExample) |
| KR (1) | KR101007497B1 (enExample) |
| CN (2) | CN102516184B (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) |
Families Citing this family (23)
| 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 |
| JP5475864B2 (ja) * | 2009-03-30 | 2014-04-16 | ドン ア ファーマシューティカル カンパニー リミテッド | ジペプチジルペプチダーゼ−ｉｖ阻害剤及び中間体の改良された製造方法 |
| SG174974A1 (en) | 2009-03-30 | 2011-11-28 | Dong A Pharm Co Ltd | Improved method for preparing 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 |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| 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 |
| US20140336196A1 (en) * | 2011-05-27 | 2014-11-13 | Merck Sharp & Dohme Corp. | Phosphoric acid salts of sitagliptin |
| WO2012170702A1 (en) | 2011-06-08 | 2012-12-13 | Arena Pharmaceuticals, Inc. | Modulators of the gpr119 receptor and the treatment of disorders related thereto |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| CN105142621A (zh) | 2012-10-24 | 2015-12-09 | 国家健康科学研究所 | 用于预防或治疗糖尿病和促进β-细胞存活的TPL2激酶抑制剂 |
| CN105555275B (zh) * | 2013-06-26 | 2021-04-20 | 东亚St株式会社 | 含有dpp-iv抑制剂的用于预防和治疗肾脏疾病的组合物 |
| 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 |
| CN107417554A (zh) * | 2017-08-15 | 2017-12-01 | 苏州信恩医药科技有限公司 | 一种依格列汀中间体的合成方法 |
| KR20220165346A (ko) | 2021-06-08 | 2022-12-15 | 동아에스티 주식회사 | 에보글립틴의 안정성이 개선된 제제 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1187342C (zh) * | 2000-05-25 | 2005-02-02 | 弗·哈夫曼-拉罗切有限公司 | 取代的1－氨基烷基内酰胺化合物及其作为毒蕈碱受体拮抗剂的用途 |
| DE60114413T2 (de) * | 2000-05-25 | 2006-07-27 | F. Hoffmann-La Roche Ag | Substituierte 1-aminoalkyl-lactame und deren verwendung als muscarinrezeptor-antagonisten |
| JP2002088070A (ja) * | 2000-09-18 | 2002-03-27 | Mitsubishi Rayon Co Ltd | 新規ピペラジノン誘導体およびその製造方法 |
| WO2004032836A2 (en) * | 2002-10-07 | 2004-04-22 | Merck & Co., Inc. | Antidiabetic beta-amino heterocylcic dipeptidyl peptidase inhibitors |
| HRP20050343A2 (en) | 2002-10-18 | 2007-03-31 | Merck & Co. Inc. | Beta-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CN1882551A (zh) | 2003-07-31 | 2006-12-20 | 麦克公司 | 用作用于治疗或预防糖尿病的二肽基肽酶－iv酶抑制剂的六氢二氮杂吖庚因酮 |
| EP1541143A1 (en) * | 2003-12-09 | 2005-06-15 | Graffinity Pharmaceuticals Aktiengesellschaft | Dpp-iv inhibitors |
| WO2005056541A1 (ja) * | 2003-12-11 | 2005-06-23 | Mitsubishi Pharma Corporation | α-アミノ酸誘導体及びその医薬用途 |
| EP1593671A1 (en) * | 2004-03-05 | 2005-11-09 | Graffinity Pharmaceuticals AG | DPP-IV inhibitors |
| EP1604989A1 (en) * | 2004-06-08 | 2005-12-14 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | DPP-IV inhibitors |
| GB0413389D0 (en) | 2004-06-16 | 2004-07-21 | Astrazeneca Ab | Chemical compounds |
| WO2006104997A2 (en) | 2005-03-29 | 2006-10-05 | Merck & Co., Inc. | Tartaric acid salts of a dipeptidyl peptidase-iv inhibitor |
| JP2008031064A (ja) * | 2006-07-27 | 2008-02-14 | Astellas Pharma Inc | ジアシルピペラジン誘導体 |
-
2008
- 2008-04-18 WO PCT/KR2008/002203 patent/WO2008130151A1/en not_active Ceased
- 2008-04-18 AU AU2008241692A patent/AU2008241692B2/en active Active
- 2008-04-18 PT PT87414488T patent/PT2142519E/pt unknown
- 2008-04-18 KR KR1020080036052A patent/KR101007497B1/ko active Active
- 2008-04-18 CN CN201110329468.1A patent/CN102516184B/zh active Active
- 2008-04-18 JP JP2010503979A patent/JP5148686B2/ja active Active
- 2008-04-18 ES ES08741448.8T patent/ES2526338T3/es active Active
- 2008-04-18 RU RU2009142602/04A patent/RU2419615C1/ru active
- 2008-04-18 NZ NZ580701A patent/NZ580701A/en unknown
- 2008-04-18 US US12/596,281 patent/US8030315B2/en active Active
- 2008-04-18 CN CN2008800126267A patent/CN101663282B/zh active Active
- 2008-04-18 MX MX2009011276A patent/MX2009011276A/es active IP Right Grant
- 2008-04-18 BR BRPI0810246-5A patent/BRPI0810246B1/pt active IP Right Grant
- 2008-04-18 CA CA2683696A patent/CA2683696C/en active Active
- 2008-04-18 EP EP08741448.8A patent/EP2142519B1/en active Active
-
2009
- 2009-10-14 IL IL201524A patent/IL201524A/en not_active IP Right Cessation
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