PE20080066A1 - BICYCLE DERIVATIVES AS CETP INHIBITORS - Google Patents
BICYCLE DERIVATIVES AS CETP INHIBITORSInfo
- Publication number
- PE20080066A1 PE20080066A1 PE2007000555A PE2007000555A PE20080066A1 PE 20080066 A1 PE20080066 A1 PE 20080066A1 PE 2007000555 A PE2007000555 A PE 2007000555A PE 2007000555 A PE2007000555 A PE 2007000555A PE 20080066 A1 PE20080066 A1 PE 20080066A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- haloalkyl
- amino
- alkyl
- tetrazol
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Abstract
SE REFIERE A COMPUESTOS BICICLICOS DE FORMULA (I) DONDE A ES UN ANILLO CARBOCICLICO(C6-C22) O HETEROCICLICO DE 5 A 14 MIEMBROS OPCIONALMENTE SUSTITUIDOS CON ALQUILO(C1-C7), HALOALQUILO(C1-C7), HALOGENO, ENTRE OTROS SUSTITUYENTES; Ar ES UN RADICAL AROMATICO CARBOCICLICO(C6-C22) OPCIONALMENTE SUSTITUIDO CON ALQUILO(C1-C7), ALCOXILO(C1-C7), HALOGENO, ENTRE OTROS SUSTITUYENTES; R1 ES C(=O)-R3, C(=O)-O-R3, S(O)m-R3, ENTRE OTROS, DONDE R3 ES H, ALQUILO(C1-C7), HALOALQUILO(C1-C7), CICLOALQUILO(C3-C7), ENTRE OTROS; m ES DE 0 A 2; X E Y SON CADA UNO N O CR6, DONDE R6 ES H, HALOGENO, CN, OH, ALQUILO(C1-C7), ENTRE OTROS; R2 ES C(=O)R3, C(=O)-O-R3, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-[(3-{N'-[3,5-BIS-(TRIFLUORO-METIL)-BENCIL]-N'-(2-METIL-2H-TETRAZOL-5-IL)-AMINO}-METIL)-QUINOLIN-2-IL]-N-(CICLOPENTIL-METIL)-ETIL-AMINA, ACIDO TRANS-[4-({N-[3-({N'-[3,5-BIS-(TRIFLUORO-METIL)-BENCIL]-N'-(2-METIL-2H-TETRAZOL-5-IL)-AMINO}-METIL)-QUINOLIN-2-IL]-N-ETIL-AMINO}-METIL)-CICLOHEXIL]-ACETICO, 3-({N-[3,5-BIS-(TRIFLUORO-METIL)-BENCIL]-N-(2-METIL-2H-TETRAZOL-5-IL)-AMINO}-METIL)-2-[N'-(CICLOPENTIL-METIL)-N'-ETIL-AMINO]-QUINOLIN-7-CARBONITRILO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROTEINA DE TRANSFERENCIA DE COLESTERIL-ESTER (CETP) SIENDO UTILES EN EL TRATAMIENTO DE HIPERLIPIDEMIA, ARTERIOESCLEROSIS, CARDIOPATIA CORONARIA, ANGINAREFERS TO BICYCLE COMPOUNDS OF FORMULA (I) WHERE A IS A CARBOCYCLIC RING (C6-C22) OR HETEROCYCLIC RING OF 5 TO 14 MEMBERS OPTIONALLY SUBSTITUTED WITH ALKYL (C1-C7), HALOALKYL (C1-CENTOS), HALOALKYL (C1-CENTOS), HALOALKyl ; Ar IS A CARBOCYCLIC AROMATIC RADICAL (C6-C22) OPTIONALLY SUBSTITUTED WITH ALKYL (C1-C7), ALCOXYL (C1-C7), HALOGEN, AMONG OTHER SUBSTITUENTS; R1 IS C (= O) -R3, C (= O) -O-R3, S (O) m-R3, AMONG OTHERS, WHERE R3 IS H, ALKYL (C1-C7), HALOALKYL (C1-C7), CYCLOALKYL (C3-C7), AMONG OTHERS; m IS 0 TO 2; X AND Y ARE EACH N O CR6, WHERE R6 IS H, HALOGEN, CN, OH, ALKYL (C1-C7), AMONG OTHERS; R2 IS C (= O) R3, C (= O) -O-R3, AMONG OTHERS. PREFERRED COMPOUNDS ARE: N - [(3- {N '- [3,5-BIS- (TRIFLUORO-METHYL) -BENZYL] -N' - (2-METHYL-2H-TETRAZOL-5-IL) -AMINE} - METHYL) -QUINOLIN-2-IL] -N- (CYCLOPENTIL-METHYL) -ETHYL-AMINE, TRANS- [4 - ({N- [3 - ({N '- [3,5-BIS- (TRIFLUORO- METHYL) -BENZYL] -N '- (2-METHYL-2H-TETRAZOL-5-IL) -AMINO} -MEthyl) -QUINOLIN-2-IL] -N-ETHYL-AMINO} -MEthyl) -CYCLOHEXIL] -ACETIC , 3 - ({N- [3,5-BIS- (TRIFLUORO-METHYL) -BENZYL] -N- (2-METHYL-2H-TETRAZOL-5-IL) -AMINO} -MEthyl) -2- [N ' - (CYCLOPENTIL-METHYL) -N'-ETHYL-AMINO] -QUINOLIN-7-CARBONITRILE, AMONG OTHERS. IT ALSO REFERS TO A PHARMACEUTICAL COMPOSITION. SAID COMPOUNDS ARE INHIBITORS OF CHOLESTERYL-ESTER TRANSFER PROTEIN (CETP), BEING USEFUL IN THE TREATMENT OF HYPERLIPIDEMIA, ARTERIOSCLEROSIS, CORONARY CARDIOPATIA, ANGINA
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0609268.8A GB0609268D0 (en) | 2006-05-10 | 2006-05-10 | Organic compounds |
US86648006P | 2006-11-20 | 2006-11-20 | |
US89614207P | 2007-03-21 | 2007-03-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20080066A1 true PE20080066A1 (en) | 2008-03-17 |
Family
ID=36637241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007000555A PE20080066A1 (en) | 2006-05-10 | 2007-05-08 | BICYCLE DERIVATIVES AS CETP INHIBITORS |
Country Status (6)
Country | Link |
---|---|
JP (1) | JP4926241B2 (en) |
CN (1) | CN101622242B (en) |
BR (1) | BRPI0711384A2 (en) |
GB (1) | GB0609268D0 (en) |
PE (1) | PE20080066A1 (en) |
RU (1) | RU2430917C2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4846769B2 (en) * | 2007-07-30 | 2011-12-28 | 田辺三菱製薬株式会社 | Pharmaceutical composition |
JPWO2014017569A1 (en) * | 2012-07-26 | 2016-07-11 | 興和株式会社 | Medicine for lowering blood LDL |
EP2919765A2 (en) * | 2012-11-19 | 2015-09-23 | Dr. Reddy's Laboratories Ltd. | Pharmaceutical compositions of cetp inhibitors |
CN103351354B (en) * | 2013-06-09 | 2015-08-12 | 西安近代化学研究所 | 1-methyl-5-amino tetrazole synthetic method |
CN103524445A (en) * | 2013-09-09 | 2014-01-22 | 南通市华峰化工有限责任公司 | Method for synthetic production of 1-methyl-5-aminotetrazole |
CN107304174B (en) * | 2016-04-21 | 2019-05-10 | 沈阳药科大学 | Disubstituted cycloalkenyl methylamine like derivative of N, N- and its preparation method and application |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003221376A (en) * | 2001-11-21 | 2003-08-05 | Japan Tobacco Inc | Cept activity inhibitor |
BR0306208A (en) * | 2002-08-30 | 2004-10-13 | Japan Tobacco Inc | Dibenzylamine compounds and their pharmaceutical use |
DK1848430T3 (en) * | 2004-12-31 | 2017-11-06 | Dr Reddys Laboratories Ltd | NEW BENZYLAMINE DERIVATIVES AS CETP INHIBITORS |
WO2007075194A1 (en) * | 2005-12-28 | 2007-07-05 | Reddy Us Therapeutics, Inc. | Selective benzylamine derivatives and their utility as cholesterol ester-transfer protein inhibitors |
UY30118A1 (en) * | 2006-01-31 | 2007-06-29 | Tanabe Seiyaku Co | AMIS TRISUSTITUDE COMPUTER |
-
2006
- 2006-05-10 GB GBGB0609268.8A patent/GB0609268D0/en not_active Ceased
-
2007
- 2007-05-08 CN CN2007800205902A patent/CN101622242B/en not_active Expired - Fee Related
- 2007-05-08 JP JP2009508242A patent/JP4926241B2/en not_active Expired - Fee Related
- 2007-05-08 PE PE2007000555A patent/PE20080066A1/en not_active Application Discontinuation
- 2007-05-08 BR BRPI0711384-6A patent/BRPI0711384A2/en not_active IP Right Cessation
- 2007-05-08 RU RU2008148290/04A patent/RU2430917C2/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
BRPI0711384A2 (en) | 2011-11-22 |
GB0609268D0 (en) | 2006-06-21 |
JP2009536172A (en) | 2009-10-08 |
RU2008148290A (en) | 2010-06-20 |
CN101622242B (en) | 2013-07-17 |
RU2430917C2 (en) | 2011-10-10 |
JP4926241B2 (en) | 2012-05-09 |
CN101622242A (en) | 2010-01-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20090982A1 (en) | PIPERIDINE DERIVATIVES AS CHOLESTERYL-ESTER TRANSFER PROTEIN (CETP) INHIBITORS | |
PE20070528A1 (en) | HETEROCYCLIC COMPOUNDS AS LIGANDS OF THE VANYLOID RECEPTOR OF SUBTYPE 1 | |
PE20080066A1 (en) | BICYCLE DERIVATIVES AS CETP INHIBITORS | |
PE20130242A1 (en) | DERIVATIVES OF ISOXAZOLO-PYRIDINE | |
PE20070585A1 (en) | SULFONAMIDE DERIVATIVES AS GLUCOKINASE ACTIVATORS | |
PE20091656A1 (en) | HETEROCYCLIC COMPOUNDS AS INHIBITORS OF RAF KINASE | |
PE20081059A1 (en) | DERIVATIVES OF PYRIMIDINES AS INHIBITORS OF THE ACTIVITY OF BRUTON'S TYROSINE KINASE (BTK) | |
PE20141375A1 (en) | GLUCOKINASE ACTIVATORS | |
PE20090601A1 (en) | PYRIDIN-IL-OXY-PYRIDINES DERIVATIVES AS ALK5 INHIBITORS | |
PE20080069A1 (en) | BICYCLE COMPOUNDS AS AGONISTS OF THE RECEPTOR 40 COUPLED TO PROTEIN G (GPR40) | |
PE20080906A1 (en) | HETEROARYL DERIVATIVES AS CYTOKINE INHIBITORS | |
PE20121050A1 (en) | N- (1- (4- (1H-PYRAZOLE-5-IL) FTALAZIN-1-IL) PIPERIDIN-4-IL) -BENZAMIDE COMPOUNDS SUBSTITUTE AS ANTAGONISTS IN THE HEDGEHOG TRAJECTORY | |
PE20051146A1 (en) | HETEROCYCLIC ANTICITOCIN COMPOUNDS | |
PE20141529A1 (en) | BICYCLE DERIVATIVES [3,2,1] OCTILAMIDE AND ITS USES | |
PE20091842A1 (en) | PYRROLIDINONES AS GLUCOKINASE ACTIVATORS | |
PE20091840A1 (en) | PYRIDYL INHIBITORS FROM THE HEDGEHOG SIGNALING | |
PE20121354A1 (en) | HEPATITIS C VIRUS INHIBITORS | |
PE20070137A1 (en) | BENZAMIDINE-DERIVED COMPOUNDS AS MODULATORS OF HYDROXIESTEROID DEHYDROGENASES | |
PE20080061A1 (en) | AMIDA-DERIVED COMPOUNDS AS INHIBITORS OF THE POTASSIUM CHANNELS TASK-1 AND TASK-3 | |
PE20060727A1 (en) | ANTHRANYLAMIDOPYRIDINES AS INHIBITORS OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR KINASE (VEGF) | |
PE20080077A1 (en) | SULFONYLPHENYL DERIVATIVES AS IL-8 RECEPTOR ANTAGONISTS | |
PE20090641A1 (en) | HETERO CYCLIC AMIDES | |
CL2011002604A1 (en) | Compounds derived from n- (cyanomethyl) -4- (sulfonyl) pyrrolidine-2-carboxamide, cathepsin s or l inhibitors; preparation procedure; pharmaceutical composition; and its use for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurism, peripheral arterial diseases or diabetic nephropathy. | |
PE20081404A1 (en) | SULFONYL-PHENYL-2H- [1,2,4] OXADIAZOL-5-ONA DERIVATIVES AND PROCESSES FOR THEIR PREPARATION | |
PE20091466A1 (en) | DERIVATIVES OF 4,5-DIHYDRO-OXAZOLE-2-IL-AMINE |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |