WO2002017912A1 - Antagonistes de l'endotheline - Google Patents
Antagonistes de l'endotheline Download PDFInfo
- Publication number
- WO2002017912A1 WO2002017912A1 PCT/US2001/027220 US0127220W WO0217912A1 WO 2002017912 A1 WO2002017912 A1 WO 2002017912A1 US 0127220 W US0127220 W US 0127220W WO 0217912 A1 WO0217912 A1 WO 0217912A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- trans
- benzodioxol
- carboxylic acid
- ethyl
- pyrrohdine
- Prior art date
Links
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- SSSXDHHNMURNSW-PCLYUOBCSA-N CCCCN(CCC[N](C)(C)C)C(CN(C[C@@H]1[C@H]2C=C(CCO3)C3=CC2)[C@@H](CCCN(CCC2)C2O)[C@@H]1C(O)=O)=O Chemical compound CCCCN(CCC[N](C)(C)C)C(CN(C[C@@H]1[C@H]2C=C(CCO3)C3=CC2)[C@@H](CCCN(CCC2)C2O)[C@@H]1C(O)=O)=O SSSXDHHNMURNSW-PCLYUOBCSA-N 0.000 description 1
- KIVNREGYHAPVKE-SZZWIKJPSA-N CCCCN(CCC[N](C)(C)C)C(CN(C[C@@H]1c(cc2)cc3c2OCO3)[C@@H](CCOc(cccc2)c2OC)[C@@H]1C(O)=O)=O Chemical compound CCCCN(CCC[N](C)(C)C)C(CN(C[C@@H]1c(cc2)cc3c2OCO3)[C@@H](CCOc(cccc2)c2OC)[C@@H]1C(O)=O)=O KIVNREGYHAPVKE-SZZWIKJPSA-N 0.000 description 1
- QRNULSMBKZIWQM-UHFFFAOYSA-N CCCCN(CCI)S(CCCC(F)(F)F)(I)=O Chemical compound CCCCN(CCI)S(CCCC(F)(F)F)(I)=O QRNULSMBKZIWQM-UHFFFAOYSA-N 0.000 description 1
- SJCBCYXDKYRDLB-RTWAWAEBSA-N CCCCN(CCN)C(CN(C1)[C@@H](CCN(CCC(N2C)=O)C2=O)C[C@H]1c1ccc2OCOc2c1)=O Chemical compound CCCCN(CCN)C(CN(C1)[C@@H](CCN(CCC(N2C)=O)C2=O)C[C@H]1c1ccc2OCOc2c1)=O SJCBCYXDKYRDLB-RTWAWAEBSA-N 0.000 description 1
- FBLWVXOQNWICAO-MQRABVPWSA-N CCCCN(CCN)C(CN(C[C@@H]1c(cc2)cc3c2OCC3)[C@@H](CCN(C(C2)=O)c3c2cccc3)[C@@H]1C(O)=O)=O Chemical compound CCCCN(CCN)C(CN(C[C@@H]1c(cc2)cc3c2OCC3)[C@@H](CCN(C(C2)=O)c3c2cccc3)[C@@H]1C(O)=O)=O FBLWVXOQNWICAO-MQRABVPWSA-N 0.000 description 1
- IIDJDIHXHRCMJG-QNONIOJKSA-N CCCCN(CCN)C(CN(C[C@@H]1c(cc2)cc3c2OCO3)[C@@H](CCN(CC)C(C)O)[C@@H]1C(O)=O)=O Chemical compound CCCCN(CCN)C(CN(C[C@@H]1c(cc2)cc3c2OCO3)[C@@H](CCN(CC)C(C)O)[C@@H]1C(O)=O)=O IIDJDIHXHRCMJG-QNONIOJKSA-N 0.000 description 1
- PTXWZLBBFOOHKM-UHFFFAOYSA-N CCCCOc(c(C)ccc1)c1NC(CI)=O Chemical compound CCCCOc(c(C)ccc1)c1NC(CI)=O PTXWZLBBFOOHKM-UHFFFAOYSA-N 0.000 description 1
- OQGOVIOQTFNAKR-UHFFFAOYSA-N CCCCc1c(cccc2)c2ccc1NC(CCC)=O Chemical compound CCCCc1c(cccc2)c2ccc1NC(CCC)=O OQGOVIOQTFNAKR-UHFFFAOYSA-N 0.000 description 1
- HEEKCEDVCMPUIV-CSIQULDISA-N CCCN(C(CN(C1)[C@@H](CCC2OCCCC2)C[C@H]1c(cc1)cc2c1OCC2)=O)OCCC Chemical compound CCCN(C(CN(C1)[C@@H](CCC2OCCCC2)C[C@H]1c(cc1)cc2c1OCC2)=O)OCCC HEEKCEDVCMPUIV-CSIQULDISA-N 0.000 description 1
- NBMINPUNEPGVRH-QFYHAUMRSA-N CCCN(C(CN(CCC1(C2)C=C(CCO3)C3=CC1)C(COc1ccccc1OC)[C@@H]2C(O)=O)=O)OCCC Chemical compound CCCN(C(CN(CCC1(C2)C=C(CCO3)C3=CC1)C(COc1ccccc1OC)[C@@H]2C(O)=O)=O)OCCC NBMINPUNEPGVRH-QFYHAUMRSA-N 0.000 description 1
- NMSCGMGOYYSFOZ-WOGSGDASSA-N CCCN(C(CN(C[C@@H]1C2=CC(OC)=C3OCOC3C2C)C2(C(CC3=CC(C)CC=N3)C2)[C@@H]1C(O)=O)=O)OCCC Chemical compound CCCN(C(CN(C[C@@H]1C2=CC(OC)=C3OCOC3C2C)C2(C(CC3=CC(C)CC=N3)C2)[C@@H]1C(O)=O)=O)OCCC NMSCGMGOYYSFOZ-WOGSGDASSA-N 0.000 description 1
- FFGXGLLMJOVTPM-MQRABVPWSA-N CCCN(C(CN(C[C@@H]1c(cc2)cc3c2OCC3)[C@@H](CCN(C(C2)=O)c3c2cccc3)[C@@H]1C(O)=O)=O)OCCC Chemical compound CCCN(C(CN(C[C@@H]1c(cc2)cc3c2OCC3)[C@@H](CCN(C(C2)=O)c3c2cccc3)[C@@H]1C(O)=O)=O)OCCC FFGXGLLMJOVTPM-MQRABVPWSA-N 0.000 description 1
- YLBXYRZHQMQVJK-UHFFFAOYSA-N CCCN(Cc1cc(OC)ccc1)C(CI)=O Chemical compound CCCN(Cc1cc(OC)ccc1)C(CI)=O YLBXYRZHQMQVJK-UHFFFAOYSA-N 0.000 description 1
- HZAPWWAYTHXHRN-UHFFFAOYSA-N CCCOC1(C)C(C)=CC=CC1NC(CI)=O Chemical compound CCCOC1(C)C(C)=CC=CC1NC(CI)=O HZAPWWAYTHXHRN-UHFFFAOYSA-N 0.000 description 1
- XRJYMHASJFSHRH-UHFFFAOYSA-N CCc(c(OC)c1)ccc1OC Chemical compound CCc(c(OC)c1)ccc1OC XRJYMHASJFSHRH-UHFFFAOYSA-N 0.000 description 1
- LAGWZWJDSQHXQZ-UHFFFAOYSA-N CCc(cc1)cc(Cl)c1Cl Chemical compound CCc(cc1)cc(Cl)c1Cl LAGWZWJDSQHXQZ-UHFFFAOYSA-N 0.000 description 1
- OGYDVZMTGABPAA-UHFFFAOYSA-N CCc(nc(C)nc1)c1F Chemical compound CCc(nc(C)nc1)c1F OGYDVZMTGABPAA-UHFFFAOYSA-N 0.000 description 1
- FYXJYERDXXUGDP-UHFFFAOYSA-N CCc1nc(C)ncc1 Chemical compound CCc1nc(C)ncc1 FYXJYERDXXUGDP-UHFFFAOYSA-N 0.000 description 1
- DWSUJONSJJTODA-UHFFFAOYSA-N ClCc(cc1)cc2c1OCO2 Chemical compound ClCc(cc1)cc2c1OCO2 DWSUJONSJJTODA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Abstract
L'invention concerne un composé correspondant à la formule (I), ou un sel pharmaceutiquement acceptable de ce composé, ainsi que des procédés et des intermédiaires pour la préparation de ce composé. L'invention concerne également un procédé pour lutter contre l'action de l'endothéline.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/653,563 US7208517B1 (en) | 1994-08-19 | 2000-08-31 | Endothelin antagonists |
US09/653,563 | 2000-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002017912A1 true WO2002017912A1 (fr) | 2002-03-07 |
Family
ID=24621388
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/027220 WO2002017912A1 (fr) | 2000-08-31 | 2001-08-31 | Antagonistes de l'endotheline |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2002017912A1 (fr) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006034085A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline de l’hydrochlorure d’atrasentan |
WO2006034084A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline 2 de l’hydrochlorure d’atrasentan |
WO2006034234A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline 3 de l’hydrochlorure d’atrasentan |
WO2006034094A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline 1 de l’hydrochlorure d’atrasentan |
WO2011114103A1 (fr) | 2010-03-18 | 2011-09-22 | Biolipox Ab | Pyrimidinones pour usage médicamenteux |
US8569341B2 (en) | 2010-06-04 | 2013-10-29 | Amgen Inc. | Piperidinone derivatives as MDM2 inhibitors for the treatment of cancer |
US8623819B2 (en) | 2007-08-22 | 2014-01-07 | AbbVie Deutschland GmbH & Co. KG | Therapy for complications of diabetes |
US8952036B2 (en) | 2013-02-28 | 2015-02-10 | Amgen Inc. | Benzoic acid derivative MDM2 inhibitor for the treatment of cancer |
US9376386B2 (en) | 2013-06-10 | 2016-06-28 | Amgen, Inc. | Processes of making and crystalline forms of a MDM2 inhibitor |
US9376425B2 (en) | 2011-09-27 | 2016-06-28 | Amgen, Inc. | Heterocyclic compounds as MDM2 inhibitors for the treatment of cancer |
CN105745204A (zh) * | 2013-09-12 | 2016-07-06 | 艾伯维公司 | 用于治疗肾脏疾病的阿曲生坦扁桃酸盐 |
US9758495B2 (en) | 2013-03-14 | 2017-09-12 | Amgen Inc. | Heteroaryl acid morpholinone compounds as MDM2 inhibitors for the treatment of cancer |
WO2018010656A1 (fr) * | 2016-07-12 | 2018-01-18 | 南京明德新药研发股份有限公司 | Dérivé de pyrrolidine servant d'agoniste de ppar |
US11396493B2 (en) | 2017-12-21 | 2022-07-26 | Guangdong Raynovent Biotech Co., Ltd. | Amorphous pyrrolidine derivative as PPAR agonist and preparation method thereof |
US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996006095A1 (fr) * | 1994-08-19 | 1996-02-29 | Abbott Laboratories | Antagonistes d'endotheline |
WO1997030046A1 (fr) * | 1996-02-13 | 1997-08-21 | Abbott Laboratories | Derives d'acide 4-(benzo-1,3-dioxolyl)-pyrrolidine-3-carboxylique utilises comme antagonistes de l'endotheline |
WO1997030045A1 (fr) * | 1996-02-13 | 1997-08-21 | Abbott Laboratories | Derives de pyrrolidine a substitution benzo-1,3-dioxolyl et benzofuranyl servant d'antagonistes de l'endotheline |
-
2001
- 2001-08-31 WO PCT/US2001/027220 patent/WO2002017912A1/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996006095A1 (fr) * | 1994-08-19 | 1996-02-29 | Abbott Laboratories | Antagonistes d'endotheline |
WO1997030046A1 (fr) * | 1996-02-13 | 1997-08-21 | Abbott Laboratories | Derives d'acide 4-(benzo-1,3-dioxolyl)-pyrrolidine-3-carboxylique utilises comme antagonistes de l'endotheline |
WO1997030045A1 (fr) * | 1996-02-13 | 1997-08-21 | Abbott Laboratories | Derives de pyrrolidine a substitution benzo-1,3-dioxolyl et benzofuranyl servant d'antagonistes de l'endotheline |
Non-Patent Citations (1)
Title |
---|
LIU, GANG ET AL: "Design, Synthesis, and Activity of a Series of Pyrrolidine-3- carboxylic Acid-Based, Highly Specific, Orally Active ETB Antagonists Containing a Diphenylmethylamine Acetamide Side Chain", J. MED. CHEM. (1999), 42(18), 3679-3689, XP002187525 * |
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9051301B2 (en) | 2004-09-17 | 2015-06-09 | Abbvie Inc. | Crystalline form of a drug |
WO2006034084A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline 2 de l’hydrochlorure d’atrasentan |
WO2006034234A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline 3 de l’hydrochlorure d’atrasentan |
WO2006034094A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline 1 de l’hydrochlorure d’atrasentan |
JP2008513481A (ja) * | 2004-09-17 | 2008-05-01 | アボット・ラボラトリーズ | アトラセンタン塩酸塩の結晶形2 |
WO2006034085A1 (fr) * | 2004-09-17 | 2006-03-30 | Abbott Laboratories | Forme cristalline de l’hydrochlorure d’atrasentan |
US8865650B2 (en) | 2007-08-22 | 2014-10-21 | AbbVie Deutschland GmbH & Co. KG | Therapy for complications of diabetes |
US8623819B2 (en) | 2007-08-22 | 2014-01-07 | AbbVie Deutschland GmbH & Co. KG | Therapy for complications of diabetes |
US9592231B2 (en) | 2007-08-22 | 2017-03-14 | AbbVie Deutschland GmbH & Co. KG | Therapy for complications of diabetes |
WO2011114103A1 (fr) | 2010-03-18 | 2011-09-22 | Biolipox Ab | Pyrimidinones pour usage médicamenteux |
US8569341B2 (en) | 2010-06-04 | 2013-10-29 | Amgen Inc. | Piperidinone derivatives as MDM2 inhibitors for the treatment of cancer |
US9296736B2 (en) | 2010-06-04 | 2016-03-29 | Amgen Inc. | Piperidinone derivatives as MDM2 inhibitors for the treatment of cancer |
US9593129B2 (en) | 2010-06-04 | 2017-03-14 | Amgen, Inc. | Piperidinone derivatives as MDM2 inhibitors for the treatment of cancer |
US9376425B2 (en) | 2011-09-27 | 2016-06-28 | Amgen, Inc. | Heterocyclic compounds as MDM2 inhibitors for the treatment of cancer |
US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
US8952036B2 (en) | 2013-02-28 | 2015-02-10 | Amgen Inc. | Benzoic acid derivative MDM2 inhibitor for the treatment of cancer |
US9758495B2 (en) | 2013-03-14 | 2017-09-12 | Amgen Inc. | Heteroaryl acid morpholinone compounds as MDM2 inhibitors for the treatment of cancer |
US9855259B2 (en) | 2013-06-10 | 2018-01-02 | Amgen Inc. | Processes of making and crystalline forms of a MDM2 inhibitor |
US9623018B2 (en) | 2013-06-10 | 2017-04-18 | Amgen Inc. | Processes of making and crystalline forms of a MDM2 inhibitor |
US9757367B2 (en) | 2013-06-10 | 2017-09-12 | Amgen Inc. | Calcium propane-2-sulfinate dihydrate |
US9801867B2 (en) | 2013-06-10 | 2017-10-31 | Amgen Inc. | Processes of making and crystalline forms of a MDM2 inhibitor |
US9376386B2 (en) | 2013-06-10 | 2016-06-28 | Amgen, Inc. | Processes of making and crystalline forms of a MDM2 inhibitor |
CN105745204A (zh) * | 2013-09-12 | 2016-07-06 | 艾伯维公司 | 用于治疗肾脏疾病的阿曲生坦扁桃酸盐 |
WO2018010656A1 (fr) * | 2016-07-12 | 2018-01-18 | 南京明德新药研发股份有限公司 | Dérivé de pyrrolidine servant d'agoniste de ppar |
CN109563032A (zh) * | 2016-07-12 | 2019-04-02 | 广东众生睿创生物科技有限公司 | 作为ppar激动剂的吡咯烷衍生物 |
US10526320B2 (en) | 2016-07-12 | 2020-01-07 | Guangdong Raynovent Biotech Co., Ltd. | Pyrrolidine derivatives as PPAR agonists |
RU2711991C1 (ru) * | 2016-07-12 | 2020-01-23 | Гуандун Рейновент Биотек Ко., Лтд. | Производные пирролидина в качестве агонистов ppar |
CN109563032B (zh) * | 2016-07-12 | 2022-05-20 | 广东众生睿创生物科技有限公司 | 作为ppar激动剂的吡咯烷衍生物 |
US11396493B2 (en) | 2017-12-21 | 2022-07-26 | Guangdong Raynovent Biotech Co., Ltd. | Amorphous pyrrolidine derivative as PPAR agonist and preparation method thereof |
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