DK2513053T3 - PYRROLIDINCARBOXYLIC ACID DERIVATIVES, PHARMACEUTICAL COMPOSITION AND METHODS OF USE IN TREATMENT OF METABOLIC DISORDERS AS AGONISTS OF G-PROTEIN CONNECTED RECEPTOR 43 (GPR43) - Google Patents
PYRROLIDINCARBOXYLIC ACID DERIVATIVES, PHARMACEUTICAL COMPOSITION AND METHODS OF USE IN TREATMENT OF METABOLIC DISORDERS AS AGONISTS OF G-PROTEIN CONNECTED RECEPTOR 43 (GPR43) Download PDFInfo
- Publication number
- DK2513053T3 DK2513053T3 DK10792934.1T DK10792934T DK2513053T3 DK 2513053 T3 DK2513053 T3 DK 2513053T3 DK 10792934 T DK10792934 T DK 10792934T DK 2513053 T3 DK2513053 T3 DK 2513053T3
- Authority
- DK
- Denmark
- Prior art keywords
- carboxylsyre
- pyrrolidin
- chlorphenyl
- biphenyl
- carbonyl
- Prior art date
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- 208000030159 metabolic disease Diseases 0.000 title abstract description 3
- 238000000034 method Methods 0.000 title description 25
- 238000011282 treatment Methods 0.000 title description 21
- 239000000556 agonist Substances 0.000 title description 14
- 239000008194 pharmaceutical composition Substances 0.000 title description 7
- NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 title 1
- -1 hydroxycarbamoyl Chemical group 0.000 claims description 1030
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 246
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 231
- 125000003118 aryl group Chemical group 0.000 claims description 210
- 125000000217 alkyl group Chemical group 0.000 claims description 194
- 125000001153 fluoro group Chemical group F* 0.000 claims description 194
- 125000005843 halogen group Chemical group 0.000 claims description 173
- 125000001072 heteroaryl group Chemical group 0.000 claims description 168
- 125000003545 alkoxy group Chemical group 0.000 claims description 156
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 148
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 144
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 133
- 125000001188 haloalkyl group Chemical group 0.000 claims description 115
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 103
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 99
- 125000000623 heterocyclic group Chemical group 0.000 claims description 97
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 96
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 95
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 93
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 93
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 92
- 150000003839 salts Chemical class 0.000 claims description 91
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 89
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims description 87
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 83
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 75
- 125000004104 aryloxy group Chemical group 0.000 claims description 67
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 claims description 65
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 64
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 63
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 61
- 125000003282 alkyl amino group Chemical group 0.000 claims description 59
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 57
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 55
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 54
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 52
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 51
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 50
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 49
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 49
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 claims description 49
- 125000004664 haloalkylsulfonylamino group Chemical group 0.000 claims description 49
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 47
- 239000004305 biphenyl Substances 0.000 claims description 46
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 45
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 44
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 41
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 40
- 125000005326 heteroaryloxy alkyl group Chemical group 0.000 claims description 36
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims description 35
- 125000005114 heteroarylalkoxy group Chemical group 0.000 claims description 35
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 34
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims description 34
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 31
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 31
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 29
- 235000010290 biphenyl Nutrition 0.000 claims description 28
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims description 28
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 28
- 125000004043 oxo group Chemical group O=* 0.000 claims description 27
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 26
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 20
- 125000005116 aryl carbamoyl group Chemical group 0.000 claims description 19
- 125000005199 aryl carbonyloxy group Chemical group 0.000 claims description 19
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 19
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims description 19
- 125000005226 heteroaryloxycarbonyl group Chemical group 0.000 claims description 19
- 125000005419 heteroarylsulfonylamino group Chemical group 0.000 claims description 19
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 19
- 125000005204 heteroarylcarbonyloxy group Chemical group 0.000 claims description 18
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 16
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 15
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims description 15
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- 206010018429 Glucose tolerance impaired Diseases 0.000 claims description 9
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 9
- 208000011580 syndromic disease Diseases 0.000 claims description 9
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 8
- 206010002383 Angina Pectoris Diseases 0.000 claims description 8
- 208000002705 Glucose Intolerance Diseases 0.000 claims description 8
- 206010022562 Intermittent claudication Diseases 0.000 claims description 8
- 208000007976 Ketosis Diseases 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- XAKBSHICSHRJCL-UHFFFAOYSA-N [CH2]C(=O)C1=CC=CC=C1 Chemical group [CH2]C(=O)C1=CC=CC=C1 XAKBSHICSHRJCL-UHFFFAOYSA-N 0.000 claims description 7
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 7
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims description 7
- 239000002671 adjuvant Substances 0.000 claims description 3
- XKTYXVDYIKIYJP-UHFFFAOYSA-N 3h-dioxole Chemical compound C1OOC=C1 XKTYXVDYIKIYJP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- VVIRTERHQQEALX-KEKNWZKVSA-N methyl (2s)-1-benzoyl-5-(2,4,6-triethylphenyl)pyrrolidine-2-carboxylate Chemical compound CCC1=CC(CC)=CC(CC)=C1C1N(C(=O)C=2C=CC=CC=2)[C@H](C(=O)OC)CC1 VVIRTERHQQEALX-KEKNWZKVSA-N 0.000 claims description 2
- PYGKYIGMDLJBJZ-KZUDCZAMSA-N methyl (2s)-1-benzoyl-5-propylpyrrolidine-2-carboxylate Chemical compound CCCC1CC[C@@H](C(=O)OC)N1C(=O)C1=CC=CC=C1 PYGKYIGMDLJBJZ-KZUDCZAMSA-N 0.000 claims description 2
- VHTLQGZJSMSREM-DLBZAZTESA-N methyl (2s,5r)-5-tert-butyl-1-(4-phenylbutanoyl)pyrrolidine-2-carboxylate Chemical compound COC(=O)[C@@H]1CC[C@H](C(C)(C)C)N1C(=O)CCCC1=CC=CC=C1 VHTLQGZJSMSREM-DLBZAZTESA-N 0.000 claims description 2
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 101100452374 Mus musculus Ikbke gene Proteins 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 206010003210 Arteriosclerosis Diseases 0.000 claims 1
- 208000004930 Fatty Liver Diseases 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 102000003817 Fos-related antigen 1 Human genes 0.000 claims 1
- 108090000123 Fos-related antigen 1 Proteins 0.000 claims 1
- PYGKYIGMDLJBJZ-KGLIPLIRSA-N methyl (2s,5r)-1-benzoyl-5-propylpyrrolidine-2-carboxylate Chemical compound CCC[C@@H]1CC[C@@H](C(=O)OC)N1C(=O)C1=CC=CC=C1 PYGKYIGMDLJBJZ-KGLIPLIRSA-N 0.000 claims 1
- BGRKNJSEAXMFPZ-MSOLQXFVSA-N methyl (2s,5r)-5-(2-chlorophenyl)-1-(3-methoxybenzoyl)pyrrolidine-2-carboxylate Chemical compound N1([C@H](CC[C@H]1C(=O)OC)C=1C(=CC=CC=1)Cl)C(=O)C1=CC=CC(OC)=C1 BGRKNJSEAXMFPZ-MSOLQXFVSA-N 0.000 claims 1
- NXGVTLNAIIXQHU-PKTZIBPZSA-N methyl (2s,5r)-5-(2-chlorophenyl)-1-[4-(2-methoxyphenyl)benzoyl]pyrrolidine-2-carboxylate Chemical compound N1([C@H](CC[C@H]1C(=O)OC)C=1C(=CC=CC=1)Cl)C(=O)C(C=C1)=CC=C1C1=CC=CC=C1OC NXGVTLNAIIXQHU-PKTZIBPZSA-N 0.000 claims 1
- PYGKYIGMDLJBJZ-KBPBESRZSA-N methyl (2s,5s)-1-benzoyl-5-propylpyrrolidine-2-carboxylate Chemical compound CCC[C@H]1CC[C@@H](C(=O)OC)N1C(=O)C1=CC=CC=C1 PYGKYIGMDLJBJZ-KBPBESRZSA-N 0.000 claims 1
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 30
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Classifications
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- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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| PCT/EP2010/070040 WO2011073376A1 (en) | 2009-12-18 | 2010-12-17 | Pyrrolidine or thiazolidine carboxylic acid derivatives, pharmaceutical composition and methods for use in treating metabolic disordersas as agonists of g- protein coupled receptor 43 (gpr43) |
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| US9828345B2 (en) | 2013-02-28 | 2017-11-28 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent ROCK1 and ROCK2 inhibitors |
| DK3074008T3 (da) * | 2013-11-27 | 2019-10-21 | Epics Therapeutics | Forbindelser, farmaceutisk sammensætning og fremgangsmåder til anvendelse i behandling af inflammation |
| CN107108581B (zh) * | 2014-08-21 | 2020-06-23 | 百时美施贵宝公司 | 作为强效rock抑制剂的回接苯甲酰胺衍生物 |
| KR101656662B1 (ko) | 2014-11-18 | 2016-09-12 | 한국생명공학연구원 | 2-옥소-1,2,3,4-테트라하이드로피리미딘-5-카르복사미드 유도체를 유효성분으로 함유하는 대사성 질환 예방 또는 치료용 약학적 조성물 |
| CN107033015B (zh) * | 2017-06-02 | 2019-04-30 | 南京欧信医药技术有限公司 | 一种药物中间体的合成方法 |
| TWI796596B (zh) | 2018-02-13 | 2023-03-21 | 美商基利科學股份有限公司 | Pd‐1/pd‐l1抑制劑 |
| KR102591947B1 (ko) | 2018-04-19 | 2023-10-25 | 길리애드 사이언시즈, 인코포레이티드 | Pd-1/pd-l1 억제제 |
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| KR20210145787A (ko) | 2019-04-02 | 2021-12-02 | 알리고스 테라퓨틱스 인코포레이티드 | Prmt5를 표적으로 하는 화합물 |
| WO2021018786A1 (en) | 2019-07-26 | 2021-02-04 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Use of ffar2 agonists for the treatment of bacterial superinfections post-viral infection |
| CN110981779B (zh) * | 2019-11-23 | 2021-02-26 | 武汉理工大学 | R-2-(2,5-二氟苯基)吡咯烷的合成方法 |
| US12528769B2 (en) | 2020-06-10 | 2026-01-20 | Epics Therapeutics | Synthesis of (2S,5R)-5-(2-chlorophenyl)-1-(2′-methoxy-[1,1′-biphenyl]-4-carbonyl)pyrrolidine-2-carboxylic acid |
| JP2023540344A (ja) | 2020-09-03 | 2023-09-22 | センテッサ ファーマシューティカルズ (オレキシア) リミテッド | 二環式複素環誘導体およびオレキシン-2受容体アゴニストとしてのそれらの使用 |
| CN120077024A (zh) | 2022-10-11 | 2025-05-30 | 艾匹克治疗公司 | (2s,5r)-5-(2-氯苯基)-1-(2'-甲氧基-[1,1'-联苯]-4-羰基)吡咯烷-2-羧酸的多晶型物及其制备方法 |
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| US3542788A (en) | 1968-06-12 | 1970-11-24 | Searle & Co | 1-amino-5-phenyl-2-pyrrolepropionic acid and congeners |
| US4006075A (en) | 1975-01-06 | 1977-02-01 | Exxon Research And Engineering Company | Method of regenerating a cracking catalyst with substantially complete combustion of carbon monoxide |
| DE3421295A1 (de) | 1984-06-08 | 1985-12-12 | Basf Ag, 6700 Ludwigshafen | Neue pyrrolidincarbonsaeurederivative, verfahren zu ihrer herstellung |
| JPH06104658B2 (ja) * | 1988-06-23 | 1994-12-21 | 三菱化成株式会社 | ピロールカルボン酸誘導体 |
| FR2678938B1 (fr) * | 1991-07-10 | 1993-10-08 | Rhone Poulenc Rorer Sa | Derives de pyrrolidine, leur preparation et les medicaments les contenant. |
| GB9206757D0 (en) | 1992-03-27 | 1992-05-13 | Ferring Bv | Novel peptide receptor ligands |
| AU1856997A (en) | 1996-02-02 | 1997-08-22 | Merck & Co., Inc. | Method for raising hdl cholesterol levels |
| JP3005469B2 (ja) | 1996-06-05 | 2000-01-31 | 住友軽金属工業株式会社 | 内面スズめっき長尺銅管の製造方法 |
| US6177464B1 (en) | 1997-03-14 | 2001-01-23 | Sepracor, Inc. | Ring opening metathesis of alkenes |
| WO2001085720A1 (en) | 2000-05-05 | 2001-11-15 | Smithkline Beecham Corporation | Novel anti-infectives |
| US7105556B2 (en) * | 2001-05-30 | 2006-09-12 | Bristol-Myers Squibb Company | Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method |
| EP1440069B1 (en) | 2001-11-02 | 2007-08-15 | Glaxo Group Limited | 4-(6-membered)-heteroaryl acyl pyrrolidine derivatives as hcv inhibitors |
| FI20030014A0 (fi) * | 2003-01-03 | 2003-01-03 | Orion Corp | Prolyylioligopeptidaasia inhiboivaa aktiivisuutta omaavia yhdisteitä |
| US20040142379A1 (en) * | 2003-01-16 | 2004-07-22 | Carlsberg Research Laboratory | Affinity fishing for ligands and proteins receptors |
| US7459472B2 (en) * | 2003-08-08 | 2008-12-02 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds, compositions, and methods of use |
| AU2004263508A1 (en) | 2003-08-08 | 2005-02-17 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds, compositions, and methods of use |
| TW200528107A (en) * | 2003-11-25 | 2005-09-01 | Nissan Chemical Ind Ltd | T-type calcium channel inhibitor |
| WO2005122379A2 (en) * | 2004-05-27 | 2005-12-22 | The Regents Of The University Of California | Alpha-4 beta-1 integrin ligands for imaging and therapy |
| SG155896A1 (en) | 2004-09-22 | 2009-10-29 | Arena Pharm Inc | Gpr43 and modulators thereof for the treatment of metabolic-related disorders |
| US7759337B2 (en) | 2005-03-03 | 2010-07-20 | Amgen Inc. | Phthalazine compounds and methods of use |
| US7425633B2 (en) * | 2005-08-26 | 2008-09-16 | National Health Research Institutes | Pyrrolidine compounds |
| US8202902B2 (en) * | 2006-05-05 | 2012-06-19 | The Regents Of The University Of Michigan | Bivalent SMAC mimetics and the uses thereof |
| US20090004140A1 (en) * | 2007-06-26 | 2009-01-01 | Yao-Ling Qiu | 4-substituted pyrrolidine as anti-infectives |
| US20090233972A1 (en) | 2008-03-12 | 2009-09-17 | Yat Sun Or | Substituted heterocycles as anti-infectives |
| US20100074863A1 (en) | 2008-09-17 | 2010-03-25 | Yat Sun Or | Anti-infective pyrrolidine derivatives and analogs |
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