JP6163695B2 - 新しいインダニルオキシフェニルシクロプロパンカルボン酸 - Google Patents
新しいインダニルオキシフェニルシクロプロパンカルボン酸 Download PDFInfo
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- JP6163695B2 JP6163695B2 JP2015514446A JP2015514446A JP6163695B2 JP 6163695 B2 JP6163695 B2 JP 6163695B2 JP 2015514446 A JP2015514446 A JP 2015514446A JP 2015514446 A JP2015514446 A JP 2015514446A JP 6163695 B2 JP6163695 B2 JP 6163695B2
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- alkyl
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- cycloalkyl
- phenyl
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- 0 CC**C([C@](C1)C1c(cc1)ccc1OC(C)(C)C)=O Chemical compound CC**C([C@](C1)C1c(cc1)ccc1OC(C)(C)C)=O 0.000 description 14
- CPZDJYXAKHRXQU-UHFFFAOYSA-N O=C(CCc1c2Br)c1ccc2OS(C(F)(F)F)(=O)=O Chemical compound O=C(CCc1c2Br)c1ccc2OS(C(F)(F)F)(=O)=O CPZDJYXAKHRXQU-UHFFFAOYSA-N 0.000 description 2
- DXCSNTMGLACOBQ-VIFPVBQESA-N Bc(c(CC[C@@H]1O)c1cc1)c1C#N Chemical compound Bc(c(CC[C@@H]1O)c1cc1)c1C#N DXCSNTMGLACOBQ-VIFPVBQESA-N 0.000 description 1
- WNPFWXJJJBWXEL-UHFFFAOYSA-N CC(C)(C(N)=O)Oc(cc1C)cc(C)c1Br Chemical compound CC(C)(C(N)=O)Oc(cc1C)cc(C)c1Br WNPFWXJJJBWXEL-UHFFFAOYSA-N 0.000 description 1
- PXBAOGPIENNIPR-UHFFFAOYSA-N CC(C)(C(O)=O)Oc(cc1C)cc(C)c1Br Chemical compound CC(C)(C(O)=O)Oc(cc1C)cc(C)c1Br PXBAOGPIENNIPR-UHFFFAOYSA-N 0.000 description 1
- GRFNSWBVXHLTCI-UHFFFAOYSA-N CC(C)(C)Oc1ccc(C=C)cc1 Chemical compound CC(C)(C)Oc1ccc(C=C)cc1 GRFNSWBVXHLTCI-UHFFFAOYSA-N 0.000 description 1
- DGRAQVSKZQNWGQ-UHFFFAOYSA-N CC(C)(COc(cc1C)cc(C)c1Br)S(C)(=O)=O Chemical compound CC(C)(COc(cc1C)cc(C)c1Br)S(C)(=O)=O DGRAQVSKZQNWGQ-UHFFFAOYSA-N 0.000 description 1
- QOPRWBRNMPANKN-UHFFFAOYSA-N COc(cc1)cc(CC2)c1C2=O Chemical compound COc(cc1)cc(CC2)c1C2=O QOPRWBRNMPANKN-UHFFFAOYSA-N 0.000 description 1
- BTWXCXOIGJXZDW-UHFFFAOYSA-N Cc(cc(cc1C)OCC2(CO)CC2)c1Br Chemical compound Cc(cc(cc1C)OCC2(CO)CC2)c1Br BTWXCXOIGJXZDW-UHFFFAOYSA-N 0.000 description 1
- FKNQCJSGGFJEIZ-UHFFFAOYSA-N Cc1ccncc1 Chemical compound Cc1ccncc1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 description 1
- OYPKKLODLDLDCJ-UHFFFAOYSA-N Cc1n[nH]c(-c(cc2C)cc(C)c2Br)n1 Chemical compound Cc1n[nH]c(-c(cc2C)cc(C)c2Br)n1 OYPKKLODLDLDCJ-UHFFFAOYSA-N 0.000 description 1
- QUBDXQOHSZEIHW-PKTZIBPZSA-N Cc1nc(-c(cc2)ccc2-c2c(CC/C3=[O]\c4ccc([C@@H](C5)[C@H]5C(O)=O)cc4)c3ccc2C(F)(F)F)n[o]1 Chemical compound Cc1nc(-c(cc2)ccc2-c2c(CC/C3=[O]\c4ccc([C@@H](C5)[C@H]5C(O)=O)cc4)c3ccc2C(F)(F)F)n[o]1 QUBDXQOHSZEIHW-PKTZIBPZSA-N 0.000 description 1
- UCDGEZNDKOOCBI-UHFFFAOYSA-N Cc1nc(-c(cc2C)cc(C)c2Br)n[n]1C Chemical compound Cc1nc(-c(cc2C)cc(C)c2Br)n[n]1C UCDGEZNDKOOCBI-UHFFFAOYSA-N 0.000 description 1
- OYWPFIUVDKHHGQ-UHFFFAOYSA-N Ic1cnccn1 Chemical compound Ic1cnccn1 OYWPFIUVDKHHGQ-UHFFFAOYSA-N 0.000 description 1
- GDONYXQZICYUPZ-UHFFFAOYSA-N N#Cc(ccc1c2CCC1=O)c2Br Chemical compound N#Cc(ccc1c2CCC1=O)c2Br GDONYXQZICYUPZ-UHFFFAOYSA-N 0.000 description 1
- ICSNLGPSRYBMBD-UHFFFAOYSA-N Nc1ccccn1 Chemical compound Nc1ccccn1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 1
- CUYKNJBYIJFRCU-UHFFFAOYSA-N Nc1cccnc1 Chemical compound Nc1cccnc1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 description 1
- LETVJWLLIMJADE-UHFFFAOYSA-N Nc1cccnn1 Chemical compound Nc1cccnn1 LETVJWLLIMJADE-UHFFFAOYSA-N 0.000 description 1
- UMBMJVDACOHHAY-FULLSBAXSA-N OC1(COc(cc2)ccc2-c2c(CC[C@H]3Oc4ccc([C@@H](C5)[C@H]5C(O)=O)cc4)c3ccc2C(F)(F)F)CCOCC1 Chemical compound OC1(COc(cc2)ccc2-c2c(CC[C@H]3Oc4ccc([C@@H](C5)[C@H]5C(O)=O)cc4)c3ccc2C(F)(F)F)CCOCC1 UMBMJVDACOHHAY-FULLSBAXSA-N 0.000 description 1
- PTPAIKGALUBHCW-UHFFFAOYSA-N Oc(c(Br)c1CC2)ccc1C2=O Chemical compound Oc(c(Br)c1CC2)ccc1C2=O PTPAIKGALUBHCW-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A61K31/425—Thiazoles
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- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
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- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
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- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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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- C07D309/10—Oxygen atoms
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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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- 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
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| EP3177282B1 (en) | 2014-08-08 | 2021-10-06 | Merck Sharp & Dohme Corp. | Antidiabetic bicyclic compounds |
| WO2016019587A1 (en) | 2014-08-08 | 2016-02-11 | Merck Sharp & Dohme Corp. | [7, 6]-fused bicyclic antidiabetic compounds |
| US10968193B2 (en) | 2014-08-08 | 2021-04-06 | Merck Sharp & Dohme Corp. | Antidiabetic bicyclic compounds |
| US10100042B2 (en) | 2014-08-08 | 2018-10-16 | Merck Sharp & Dohme Corp. | [5,6]—fused bicyclic antidiabetic compounds |
| MX389591B (es) | 2014-08-29 | 2025-03-20 | Tes Pharma S R L | INHIBIDORES DE ACIDO A-AMINO-ß-CARBOXIMUCONICO SEMIALDEHIDO DESCARBOXILASA |
| JP6816107B2 (ja) * | 2015-08-07 | 2021-01-20 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | インダニルアミノピリジルシクロプロパンカルボン酸、医薬組成物及びこれらの使用 |
| CN107216317B (zh) * | 2016-03-21 | 2020-04-07 | 上海医药工业研究院 | 一种阿法替尼中间体的制备方法 |
| WO2018077699A1 (en) | 2016-10-25 | 2018-05-03 | Boehringer Ingelheim International Gmbh | Benzylaminopyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof |
| EP3544958B1 (en) | 2016-11-28 | 2021-03-24 | Boehringer Ingelheim International GmbH | Indanylaminopyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof |
| KR102007633B1 (ko) | 2016-12-15 | 2019-08-06 | 일동제약(주) | 신규 페닐 프로피온 산 유도체 및 이의 용도 |
| WO2018138029A1 (en) | 2017-01-26 | 2018-08-02 | Boehringer Ingelheim International Gmbh | Benzyloxypyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof |
| JP7049349B2 (ja) * | 2017-01-26 | 2022-04-06 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ベンジルアミノピラジニルシクロプロパンカルボン酸、その医薬組成物及び使用 |
| WO2018138030A1 (en) * | 2017-01-26 | 2018-08-02 | Boehringer Ingelheim International Gmbh | Benzyloxypyrazinylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof |
| US10919859B2 (en) | 2017-01-26 | 2021-02-16 | Boehringer Ingelheim International Gmbh | Benzylaminopyridylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof |
| EP3573965B1 (en) * | 2017-01-26 | 2021-06-23 | Boehringer Ingelheim International GmbH | Indanylaminopyrazinylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof |
| US10550127B1 (en) | 2017-02-08 | 2020-02-04 | Boehringer Ingelheim International Gmbh | Indanylaminoazadihydrobenzofuranylacetic acids, pharmaceutical compositions for the treatment of diabetes |
| JOP20180040A1 (ar) * | 2017-04-20 | 2019-01-30 | Gilead Sciences Inc | مثبطات pd-1/pd-l1 |
| KR102708681B1 (ko) | 2018-02-13 | 2024-09-26 | 길리애드 사이언시즈, 인코포레이티드 | Pd-1/pd-l1 억제제 |
| US12083118B2 (en) | 2018-03-29 | 2024-09-10 | Arbutus Biopharma Corporation | Substituted 1,1′-biphenyl compounds, analogues thereof, and methods using same |
| EP3781556B1 (en) | 2018-04-19 | 2025-06-18 | Gilead Sciences, Inc. | Pd-1/pd-l1 inhibitors |
| CN118221646A (zh) | 2018-07-13 | 2024-06-21 | 吉利德科学公司 | Pd-1/pd-l1抑制剂 |
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| US628476A (en) | 1898-03-18 | 1899-07-11 | Joseph Howard Kirk | Junction of cycle, motor-car, or other frames, &c. |
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| US7834013B2 (en) * | 2003-11-19 | 2010-11-16 | Glaxosmithkline Llc | Aminophenylcyclopropyl carboxylic acids and derivatives as agonists to GPR40 |
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| WO2005063729A1 (en) | 2003-12-25 | 2005-07-14 | Takeda Pharmaceutical Company Limited | 3-(4-benzyloxyphenyl)propanoic acid derivatives |
| WO2005087710A1 (ja) * | 2004-03-15 | 2005-09-22 | Takeda Pharmaceutical Company Limited | アミノフェニルプロパン酸誘導体 |
| DE102004017930A1 (de) | 2004-04-14 | 2005-11-03 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
| ATE517867T1 (de) | 2005-02-15 | 2011-08-15 | Glaxo Group Ltd | Verbindungen, die den glutamatrezeptor verstärken und anwendungen davon in der medizin |
| EP1866278A1 (en) | 2005-03-28 | 2007-12-19 | Pfizer, Inc. | Substituted aryloxoethyl cyclopropanecarboxamide compounds as vr1 receptor antagonists |
| ES2424651T3 (es) | 2005-08-24 | 2013-10-07 | Eisai R&D Management Co., Ltd. | Nuevo derivado de piridina y derivado de pirimidina (3) |
| CA2621949A1 (en) | 2005-09-14 | 2007-03-22 | Amgen Inc. | Conformationally constrained 3- (4-hydroxy-phenyl) - substituted-propanoic acids useful for treating metabolic disorders |
| JP2009530237A (ja) | 2006-03-15 | 2009-08-27 | ノイロサーチ アクティーゼルスカブ | キナゾリノン及びカリウムチャネル活性化剤としてのその使用 |
| CN101489984B (zh) | 2006-07-18 | 2013-04-03 | 安斯泰来制药株式会社 | 氨基茚满衍生物或其盐 |
| WO2009157418A1 (ja) * | 2008-06-25 | 2009-12-30 | 第一三共株式会社 | カルボン酸化合物 |
| US8586607B2 (en) * | 2008-07-28 | 2013-11-19 | Syddansk Universitet | Compounds for the treatment of metabolic diseases |
| US20110269783A1 (en) | 2008-11-10 | 2011-11-03 | Neurosearch A/S | Novel 2,3-diamino-quinazolinone derivatives and their medical use |
| KR20110117146A (ko) | 2009-01-22 | 2011-10-26 | 라퀄리아 파마 인코포레이티드 | Cb2 수용체 효능활성이 있는 n-치환 포화 헤테로사이클릭 술폰 화합물 |
| US8389580B2 (en) * | 2009-06-02 | 2013-03-05 | Duke University | Arylcyclopropylamines and methods of use |
| US20120172351A1 (en) * | 2009-06-09 | 2012-07-05 | Nobuyuki Negoro | Novel fused cyclic compound and use thereof |
| WO2011094890A1 (en) | 2010-02-02 | 2011-08-11 | Argusina Inc. | Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators |
| WO2011103189A1 (en) | 2010-02-16 | 2011-08-25 | Uwm Research Foundation, Inc. | Methods of reducing virulence in bacteria |
| JP5780528B2 (ja) | 2010-02-19 | 2015-09-16 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 三環式ピリジン誘導体、このような化合物を含有する医薬、それらの使用、およびそれらの調製方法 |
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| US8633182B2 (en) | 2014-01-21 |
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