AR107426A1 - DERIVADOS DE N-INDEN-AMIDA COMO MODULADORES DEL mGluR7 - Google Patents
DERIVADOS DE N-INDEN-AMIDA COMO MODULADORES DEL mGluR7Info
- Publication number
- AR107426A1 AR107426A1 ARP170100186A ARP170100186A AR107426A1 AR 107426 A1 AR107426 A1 AR 107426A1 AR P170100186 A ARP170100186 A AR P170100186A AR P170100186 A ARP170100186 A AR P170100186A AR 107426 A1 AR107426 A1 AR 107426A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- alkyl
- heterocyclic ring
- halogen
- cycloalkyl
- Prior art date
Links
- 102100038294 Metabotropic glutamate receptor 7 Human genes 0.000 title 1
- 108010038449 metabotropic glutamate receptor 7 Proteins 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 22
- 229910052757 nitrogen Inorganic materials 0.000 abstract 19
- 125000001424 substituent group Chemical group 0.000 abstract 17
- 229910052736 halogen Inorganic materials 0.000 abstract 16
- 150000002367 halogens Chemical class 0.000 abstract 16
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 14
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 12
- 125000005842 heteroatom Chemical group 0.000 abstract 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 12
- 125000004981 cycloalkylmethyl group Chemical group 0.000 abstract 10
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 10
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 150000002431 hydrogen Chemical class 0.000 abstract 8
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 8
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 8
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 7
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 125000006661 (C4-C6) heterocyclic group Chemical group 0.000 abstract 4
- -1 -CH2OH Chemical group 0.000 abstract 4
- 125000002837 carbocyclic group Chemical group 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 239000011593 sulfur Substances 0.000 abstract 3
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 208000016621 Hearing disease Diseases 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- 229910052731 fluorine Chemical group 0.000 abstract 1
- 239000011737 fluorine Chemical group 0.000 abstract 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- RVTDZOWLSQQSBW-IRXDYDNUSA-N n-[(1s,2s)-1-amino-2,3-dihydro-1h-inden-2-yl]-1-(4-fluorophenyl)cyclopropane-1-carboxamide Chemical compound N([C@@H]1[C@H](C2=CC=CC=C2C1)N)C(=O)C1(C=2C=CC(F)=CC=2)CC1 RVTDZOWLSQQSBW-IRXDYDNUSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/41—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
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- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/36—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/23—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
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Abstract
Procesos para su preparación, composiciones farmacéuticas que los contienen y su uso en la terapia de trastornos auditivos y del SNC. Reivindicación 1: Un compuesto de fórmula (1) donde R¹ representa hidroxilo, -CH₂OH, ciano, -SO₂R¹ᵃ, -(CH₂)ₘ-(O)ₙ-R⁵ o (CH₂)ₚNR⁶R⁷; m es 0 ó 1; n es 0 ó 1; p es 0 ó 1; R¹ᵃ representa alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆; cada uno de R² y R³ representa independientemente hidrógeno, halógeno, fluorometilo, difluorometilo, trifluorometilo, metoxi, fluorometoxi, difluorometoxi o trifluorometoxi; cualquier R⁴ᵃ representa (X)ₜ-(CH₂)ᵛ-R¹⁶ o -CH₂O-R¹⁷ y R⁴ᵇ representa hidrógeno, metilo o flúor, o R⁴ᵃ y R⁴ᵇ, junto con el átomo de carbono al cual se acoplan, forman un anillo heterocíclico o carbocíclico saturado de 3 a 6 miembros, donde el anillo heterocíclico comprende al menos un heteroátomo anular que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo carbocíclico o heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno, oxo, alquilo C₁₋₃, alcoxi C₁₋₃, amino, metilamino, dimetilamino y haloalquilo C₁₋₃; R⁵ representa un grupo cicloalquilo C₃₋₆, un anillo heterocíclico de 4 a 6 miembros que contiene un heteroátomo anular individual que es un átomo de nitrógeno donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente seleccionado de halógeno, alquilo C₁₋₃ y haloalquilo C₁₋₃ o un grupo alquilo C₁₋₆ que no está sustituido o está sustituido con al menos un sustituyente seleccionado de cicloalquilo C₃₋₆, NR²²R²³ y un anillo heterocíclico saturado de 4 a 6 miembros que comprende al menos un heteroátomo anular que se selecciona de átomos de nitrógeno y oxígeno, donde dicho anillo heterocíclico no está sustituido o está sustituido con halógeno; cada uno de R⁶ y R⁷ representa independientemente hidrógeno, -(CH₂)q-R⁸, -SO₂R⁹, alquilo C₁₋₆, alquilcarbonilo C₁₋₆, cicloalquilcarbonilo C₃₋₆ o alcoxicarbonilo C₁₋₆, donde cada uno de los restos alquilo, cicloalquilo o alcoxi en los últimos cuatro sustituyentes no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno, alcoxi C₁₋₄ y -NR¹⁰R¹¹, o R⁶ y R⁷, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado o no saturado de 4 a 7 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de nitrógeno, oxígeno y azufre, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno, ciano, alquilo C₁₋₆, cicloalquilo C₃₋₆, cicloalquilmetilo C₃₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, cicloalquiloxi C₃₋₆, cicloalquilmetiloxi C₃₋₆ y -NR¹²R¹³; q es 0, 1 ó 2; R⁸ representa un anillo carbocíclico o heterocíclico saturado o no saturado de 3 a 6 miembros donde el anillo heterocíclico comprende de 1 a 4 heteroátomos anulares que se seleccionan independientemente de nitrógeno, oxígeno y azufre, donde el anillo carbocíclico o heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno, ciano, alquilo C₁₋₆, cicloalquilo C₃₋₆, cicloalquilmetilo C₃₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, cicloalquiloxi C₃₋₆, cicloalquilmetiloxi C₃₋₆ y -NR¹⁴R¹⁵; R⁹ representa alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, cada uno de los cuales no está sustituido o está sustituido con al menos un átomo de halógeno; cada uno de R¹⁰ y R¹¹ representa independientemente hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, o R¹⁰ y R¹¹, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado de 4 a 6 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alquilo C₁₋₃; cada uno de R¹² y R¹³ representa independientemente hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, o R¹² y R¹³, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado de 4 a 6 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alquilo C₁₋₃; cada uno de R¹⁴ y R¹⁵ representa independientemente hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, o R¹⁴ y R¹⁵, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado de 4 a 6 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alquilo C₁₋₃; t es 0 ó 1; v es 0, 1 ó 2; R¹⁶ representa -R¹⁷, -NR¹⁸R¹⁹ o un anillo heterocíclico saturado o no saturado de 4 a 6 miembros que comprende de 1 a 4 heteroátomos anulares que se seleccionan independientemente de nitrógeno, oxígeno y azufre, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente seleccionado de oxo, halógeno, ciano, fluorometoxi, difluorometoxi, trifluorometoxi, alquilo C₁₋₆, alcoxi C₁₋₆ y haloalquilo C₁₋₆; X es O, NH, -NHC(O)-, -NHC(O)O-, -C(O)NH-, -NHSO₂- o -SO₂NH-, siempre que cuando X sea O, NH, -C(O)NH- o -SO₂NH- y R¹⁶ represente -NR¹⁸R¹⁹, v sea 2; R¹⁷ representa alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, cada uno de los cuales no está sustituido o está sustituido con al menos un sustituyente que se selecciona de hidroxilo, halógeno y -NR²⁰R²¹; cada uno de R¹⁸ y R¹⁹ representa independientemente hidrógeno, alquilo C₁₋₆, alquilcarbonilo C₁₋₆, cicloalquilcarbonilo C₃₋₆, alquilsulfonilo C₁₋₆ o cicloalquilsulfonilo C₃₋₆, donde cada uno de los restos alquilo o cicloalquilo en los últimos cinco sustituyentes no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alcoxi C₁₋₄, o R¹⁸ y R¹⁹, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado de 4 a 6 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alquilo C₁₋₃; cada uno de R²⁰ y R²¹ representa independientemente hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, o R²⁰ y R²¹, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado de 4 a 6 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alquilo C₁₋₃; y cada uno de R²² y R²³ representa independientemente hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₆ o cicloalquilmetilo C₃₋₆, o R²² y R²³, junto con el átomo de nitrógeno al cual se acoplan, forman un anillo heterocíclico saturado de 4 a 6 miembros que comprende opcionalmente un heteroátomo anular adicional que se selecciona de átomos de nitrógeno y oxígeno, donde el anillo heterocíclico no está sustituido o está sustituido con al menos un sustituyente que se selecciona de halógeno y alquilo C₁₋₃; siempre que el compuesto de fórmula (1) no sea N-[(1S,2S)-1-amino-2,3-dihidro-1H-inden-2-il]-1-(4-fluorofenil)ciclopropano-1-carboxamida; o una sal farmacéuticamente aceptable de este.
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| JP7453365B2 (ja) * | 2020-05-29 | 2024-03-19 | 富士フイルム富山化学株式会社 | 高純度のn-(5-メトキシ―2-フェノキシフェニル)メタンスルホンアミド及びその製造方法 |
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| DE4220353A1 (de) * | 1992-06-22 | 1993-12-23 | Boehringer Ingelheim Kg | Verwendung carbocyclisch und heterocyclisch annelierter Dihydropyridine als Mittel mit antiproliferativer Wirkung |
| CA2138788A1 (en) * | 1992-06-22 | 1994-01-06 | Dietrich Arndts | Ring-closed dihydropyridines and their use in the preparation of pharmaceutical compositions |
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| DE10108307A1 (de) * | 2001-02-21 | 2002-08-29 | Gruenenthal Gmbh | Substituierte Propan-1,3-diamin-Derivate |
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| EP1388342A1 (en) * | 2002-08-07 | 2004-02-11 | Aventis Pharma Deutschland GmbH | Acylated, heteroaryl-condensed cycloalkenylamines and their use as pharmaceuticals |
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| Publication number | Publication date |
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| KR20180108600A (ko) | 2018-10-04 |
| EP3408256A1 (en) | 2018-12-05 |
| ECSP18056196A (es) | 2018-08-31 |
| WO2017131221A1 (en) | 2017-08-03 |
| CA3012443A1 (en) | 2017-08-03 |
| UY37084A (es) | 2017-08-31 |
| GB201601301D0 (en) | 2016-03-09 |
| US20190031599A1 (en) | 2019-01-31 |
| CO2018007610A2 (es) | 2018-07-31 |
| MA43922A (fr) | 2018-12-05 |
| JP2019508390A (ja) | 2019-03-28 |
| HK1257091A1 (zh) | 2019-10-11 |
| PE20181333A1 (es) | 2018-08-20 |
| ZA201803520B (en) | 2019-03-27 |
| CN108602760A (zh) | 2018-09-28 |
| CL2018002010A1 (es) | 2019-03-15 |
| MX2018009078A (es) | 2018-11-09 |
| EA201891680A1 (ru) | 2019-01-31 |
| SG11201804899YA (en) | 2018-07-30 |
| TN2018000175A1 (en) | 2019-10-04 |
| AU2017210803A1 (en) | 2018-07-19 |
| TW201733977A (zh) | 2017-10-01 |
| PH12018501563A1 (en) | 2019-05-15 |
| BR112018015247A2 (pt) | 2018-12-18 |
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