AR066911A1 - Derivados de piperidina / piperazina - Google Patents
Derivados de piperidina / piperazinaInfo
- Publication number
- AR066911A1 AR066911A1 ARP080102427A ARP080102427A AR066911A1 AR 066911 A1 AR066911 A1 AR 066911A1 AR P080102427 A ARP080102427 A AR P080102427A AR P080102427 A ARP080102427 A AR P080102427A AR 066911 A1 AR066911 A1 AR 066911A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- nrx
- aryl
- het
- optionally substituted
- Prior art date
Links
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical class C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 title 1
- 229940066771 systemic antihistamines piperazine derivative Drugs 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 28
- 125000003545 alkoxy group Chemical group 0.000 abstract 19
- 125000003118 aryl group Chemical group 0.000 abstract 17
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 10
- 229910052717 sulfur Inorganic materials 0.000 abstract 10
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 8
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 5
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000005842 heteroatom Chemical group 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 5
- 125000001624 naphthyl group Chemical group 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 125000000169 tricyclic heterocycle group Chemical group 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000004104 aryloxy group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 3
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 2
- 125000005871 1,3-benzodioxolyl group Chemical group 0.000 abstract 2
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- -1 2,3-dihydrobenzofuranyl Chemical group 0.000 abstract 1
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 102100036869 Diacylglycerol O-acyltransferase 1 Human genes 0.000 abstract 1
- 108050004099 Diacylglycerol O-acyltransferase 1 Proteins 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/205—Radicals derived from carbonic acid
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- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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- C07D213/72—Nitrogen atoms
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Abstract
Además, se refiere a métodos para preparar tales compuestos, composiciones farmacéuticas que comprenden dichos compuestos así como al uso como medicamentos de dichos compuestos, inhibidores de DGAT. Reivindicacion 1: Un compuesto de formula (1) que incluye cualquier forma estereoquímicamente isomérica del mismo, donde A representa CH o N; la línea punteada representa un enlace opcional en el caso en que A represente un átomo de carbono; X representa -C(=O)-; -O-C(=O)-; -C(=O)-C(=O)-; NRx-C(=O)-; -Z1-C(=O)-; -Z1-NRx-C(=O)-, -C(=O)-Z1-; -NRx-C(=O)-Z1, -S(=O)p-; -C(=S)-; -NRx-C(=S)-; -Z1-C(=S)-; -Z1-NRx-C(=S)-; -C(=S)-Z1-; -NRx-C(=S)-Z1-; Z1 representa un radical bivalente seleccionado de alcandiilo C1-6, alquendiilo C2-6 o alquindiilo C2-6; donde cada uno de dicho alcandiilo C1-6, alquendiilo C2-6 o alquindiilo C2-6 puede estar opcionalmente sustituido con hidroxilo o amino; y donde dos átomos de hidrogeno unidos al mismo carbono en el alcandiilo C1-6 pueden opcionalmente reemplazarse con alcandiilo C1-6; Y representa NRx-C(=O)-Z2-; -NRx-C(=O)-Z2-NRy-; -NRx-C(=O)-Z2-NRy-C(=O)-; -NRx-C(=O)-O-Z2-NRy-C(=O)-O-; -NRx-C(=O)-Z2-O-C(=O)-, -NRx-C(=O)-Z2-C(=O)-; -NRx-C(=O)Z2-C(=O)-O-; -NRx-C(=O)-O-Z2-C(=O)-; -NRx-C(=O)-O-Z2-C(=O)-O-, -NRx-C(=O)-O-Z2-O-C(=O)-;-NRx-C(=O)-Z2-C(=O)-NRy-; -NRc-C(=O)-Z2-NRy-C(=O)-NRy-; -C(=O)-Z2-; -C(=O)-Z2-O-; -C(=O)-NRx-Z2; -C(=O)-NRx-Z2-O-; -C(=O)-NRx-Z2-C(=O)-O-; -C(=O)-NRx-Z2-O-C(=O)-; -C(=O)-NRx-O-Z2-; -C(=O)-NRx-Z2-NRy-; -C(=O)-NRx-Z2-NRy-C(=O)-; -C(=O)-NRx-Z2-NRy-C(=O)-O-; Z2 representa un radical bivalente seleccionado de alcandiilo C1-6, alquendiilo C2-6 o alquindiilo C2-6; donde cada uno de dicho alcandiilo C1-6, alquendiilo C2-6 o alquindiilo C2-6 puede estar opcionalmente sustituido con alquiloxi C1-4, alquiltio C1-4, hidroxilo, ciano o arilo; y donde dos átomos de hidrogeno unidos al mismo átomo de carbono en la definicion de Z2 pueden opcionalmente reemplazarse con alcandiilo C1-6; Rx representa hidrogeno o alquilo C1-4; Ry representa hidrogeno; alquilo C1-4 opcionalmente sustituido con cicloalquilo C3-6 o arilo o Het; alquenilo C2-4 o -S(=O)p-ariIo; R1 representa alquilo C1-12 opcionalmente sustituido con ciano, alquiloxi C1-4, alquil-oxi C1-4-alquiloxi C1-4, cicloalquilo C3-6 o arilo; alquenilo C2-6; alquinilo C2-6; cicloalquilo C3-6; adamantanilo; arilo1, aril1alquilo C1-6; Het1 o Het1alquilo C1-6; con la salvedad de que cuando Y representa -NRx-C(=O)Z2-; -NRx-C(=O)Z2-NRy-; -NRx-C(=O)-Z2-C(=O)-NRy-; -C(=O)-Z2-; -NRx-C(=O)-Z2-NRy-C(=O)-NRy-; -C(=O)-NRx-Z2; -C(=O)-NRx-O-Z2-; o -C(=O)-NRx-Z2-NRy-; o entonces R1 puede también representar hidrogeno; R2 representa hidrogeno, alquilo C1-12, alquenilo C2-6 o R3; R3 representa cicloalquilo C3-6, fenilo, naftalenilo, 2,3-dihidro-1,4-benzodioxinilo, 1,3-benzodioxolilo, 2,3-dihidrobenzofuranilo o un heterociclo aromático de 6 miembros que contiene 1 o 2 átomos de N, donde dicho cicloalquilo C3-6, fenilo, naftalenilo, 2,3-dihidro-1,4-benzodioxinilo, 1,3-benzodioxolilo o heterociclo aromático de 6 miembros que contiene 1 o 2 átomos de N puede estar opcionalmente sustituido con al menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, seleccionándose cada sustituyente en forma independiente de hidroxilo; carboxilo; halo; alquilo C1-6 opcionalmente sustituido con hidroxi; polihaloalquilo C1-6; alquiloxi C1-6 opcionalmente sustituido con alquiloxi C1-4; alquiltio C1-6; polihalo-alquiloxi C1-6; alquiloxicarbonilo C1-6 donde alquilo C1-6 puede estar opcionalmente sustituido con arilo; ciano; alquilcarbonilo C1-6; nitro: amino, mono o di(alquil C1-4)amino; alquilcarbonilamino C1-4; -S(=O)p-alquilo C1-4; R5R4N-C(=O)-; R5R4N-alquilo C1-6; cicloalquilo C3-6; cicloalquil C3-6-alquilo C1-4; cicloalquil C3-6-C(=O)-; arilo: ariloxi; arilalquilo C1-4; aril-C(=O)-alquilo C1-4; aril-C(=O)-; Het; Het-alquilo C1-4; Het-C(=O)-alquilo C1-4; Het-C(=O)-; Het-O-; R4 representa hidrogeno; alquilo C1-4 opcionalmente sustituido con hidroxilo o alquiloxi C1-4; R7R6N-alquilo C1-4; alquiloxi C1-4; Het; Het-alquilo C1-4; arilo; R7R6N-C(=O)-alquilo C1-4; R5 representa hidrogeno o alquilo C1-4; R6 representa hidrogeno; alquilo C1-4; alquilcarbonilo C1-4; R7 representa hidrogeno o alquilo C1-4; o R6 y R7 pueden tomarse junto con el nitrogeno al que están unidos para formar un heterociclo monocíclico saturado de 5, 6 o 7 miembros que puede además contener uno o más heteroátomos seleccionados en forma independiente de O, S, S(=O)p o N; y dicho heterociclo puede estar opcionalmente sustituido con alquilo C1-4; R8 representa hidrogeno, halo, alquilo C1-4, alquilo C1-4 sustituido con hidroxilo; arilo representa fenilo o fenilo sustituido con al menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, seleccionándose cada sustituyente en forma independiente de hidroxilo; carboxilo; halo; alquilo C1-6 opcionalmente sustituido con alquiloxi C1-4, amino o mono o di(alquil C1-4)amino; polihaloalquilo C1-6; alquiloxi C1-6 opcionalmente sustituido con alquiloxi C1-4; alquiltio C1-6; polihaloalquiloxi C1-6; alquiloxicarbonilo C1-6; ciano; aminocarbonilo; mono o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono o di(alquil C1-4)amino; -S(=O)-alquilo C1-4; arilo1 representa fenilo, naftalenilo o fluorenilo; cada fenilo, naftalenilo o fluorenilo está opcionalmente sustituido con al menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, seleccionándose cada uno en forma independiente de hidroxilo; oxo; carboxilo; halo; alquilo C1-6 opcionalmente sustituido con carboxilo, alcoxicarbonilo C1-4 o aril-C(=O)-; hidroxialquilo C1-6 opcionalmente sustituido con arilo o aril-C(=O)-; polihaloalquilo C1-6; alquiloxi C1-6 opcionalmente sustituido con alquiloxi C1-4; alquiltio C1-6; polihaloalquiloxi C1-6; alquiloxi C1-6-carbonilo donde alquilo C1-6 puede estar opcionalmente sustituido con arilo; ciano; aminocarbonilo; mono o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono o di(alquil C1-6)amino; R5R4N-alquilo C1-6; cicloalquil C3-6-NRx-; aril-NRx-; Het-NRx-; cicloalquil C3-6-alquil C1-4-NRx-; arilalquil C1-4-NRx; Het-alquil C1-4-NRx; -S(=O)p-alquilo C1-4; cicloalquilo C3-6; cicloalquil C3-6-alquilo C1-4; cicloalquil C3-6-C(=O)-; arilo; ariloxi; arilalquilo C1-4; aril-C(=O)-alquilo C1-4; aril-C(=O)-; Het; Het-alquilo C1-4; Het-C(=O)-alquilo C1-4; Het-C(=O)-; Het-O-; Het representa un heterociclo monocíclico no aromático o aromático que contiene al menos un heteroátomo seleccionado en forma independiente de O, S, S(=O)p o N; o un heterociclo bicíclico o tricíclico no aromático o aromático que contiene al menos un heteroátomo seleccionado en forma independiente de O, S, S(=O)p o N; dicho heterociclo monocíclico o dicho heterociclo bi o tricíclico está opcionalmente sustituido con al menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, seleccionándose cada uno en forma independiente de hidroxilo; oxo; carboxilo; halo; alquilo C1-6 opcionalmente sustituido con alquiloxi C1-4, amino o mono o di(alquil C1-4)amino; polihaloalquilo C1-6; alquiloxi C1-6 opcionalmente sustituido con alquiloxi C1-4; alquiltio C1-6; polihaloalquiloxi C1-6; alquil C1-6-oxicarbonilo; ciano; aminocarbonilo; mono o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono o di(alquil C1-4)amino; -S(=O)p-alquilo C1-4; Het1 representa un heterociclo monocíclico no aromático o aromático que contiene al menos un heteroátomo seleccionado en forma independiente de O, S, S(=O)p- o N; o un heterociclo bicíclico o tricíclico no aromático o aromático que contiene al menos un heteroátomo seleccionado en forma independiente de O, S, S(=O)p o N; dicho heterociclo monocíclico o dicho heterociclo bi o tricíclico está opcionalmente sustituido con al menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, seleccionándose cada uno en forma independiente de hidroxilo: oxo; carboxilo; halo; alquilo C1-6 opcionalmente sustituido con carboxilo, alcoxicarbonilo C1-4 o aril-C(=O)-; hidroxialquilo C1-6 opcionalmente sustituido con arilo o aril-C(=O)-; polihaloalquilo C1-6; alquiloxi C1-6 opcionalmente sustituido con alquiloxi C1-4; alquiltio C1-6; polihaloalquiloxi C1-6; alquiloxi C1-6-carbonilo donde alquilo C1-6 puede estar opcionalmente sustituido con arilo; ciano; aminocarbonilo; mono o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono o di(alquil C1-6)amino; R5R4N-alquilo C1-6; cicloalquil C3-6-NRx-; aril-NRx-; Het-NRx-; cicloalquil C3-6- alquil C1-4-NRx-; arilalquil C1-4-NRx-; Hetalquil C1-4-NRx-; -S(=O)p-alquilo C1-4; cicloalquilo C3-6; cicloalquil C3-6-alquilo C1-4; cicloalquil C3-6-C(=O)-; arilo; ariloxi; arilalquilo C1-4; aril-C(=O)-alquilo C1-4; aril-C(=O)-; Het; Het-alquilo C1-4; Het-C(=O)-alquilo C1-4; Het-C(=O)-; Het-O-; p representa 1 o 2: con la salvedad de que si X representa -O-C(=O)-, entonces R2 representa R3; y con la salvedad de que se excluye el compuesto de formula (2), un N-oxido de los mismos, una sal aceptable para uso farmacéutico de los mismos o un solvato de los mismos.
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| JO2972B1 (en) | 2007-06-08 | 2016-03-15 | جانسين فارماسوتيكا ان. في | Piperidine / piperazine derivatives |
| ES2483898T3 (es) | 2007-06-08 | 2014-08-08 | Janssen Pharmaceutica, N.V. | Derivados de piperidina/piperazina |
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| AU2008258487A1 (en) | 2008-12-11 |
| RU2009148320A (ru) | 2011-07-20 |
| AU2008258487B2 (en) | 2012-11-15 |
| JP2010529089A (ja) | 2010-08-26 |
| WO2008148868A1 (en) | 2008-12-11 |
| WO2008148868A8 (en) | 2009-03-05 |
| CA2687754C (en) | 2015-12-08 |
| CN101678019A (zh) | 2010-03-24 |
| PE20090362A1 (es) | 2009-04-04 |
| CA2687754A1 (en) | 2008-12-11 |
| PA8783601A1 (es) | 2009-01-23 |
| US8981094B2 (en) | 2015-03-17 |
| ES2536406T3 (es) | 2015-05-25 |
| RU2470017C2 (ru) | 2012-12-20 |
| JP5385263B2 (ja) | 2014-01-08 |
| TW200911771A (en) | 2009-03-16 |
| CL2008001671A1 (es) | 2009-07-17 |
| TWI426070B (zh) | 2014-02-11 |
| CN101678019B (zh) | 2016-03-30 |
| EP2152270A1 (en) | 2010-02-17 |
| US20100190789A1 (en) | 2010-07-29 |
| EP2152270B1 (en) | 2015-03-04 |
| BRPI0813331A2 (pt) | 2014-12-23 |
| MX2009013335A (es) | 2010-01-20 |
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