AR116939A1 - 2-amino-n-heteroaril-nicotinamidas como inhibidores de nav1.8 - Google Patents
2-amino-n-heteroaril-nicotinamidas como inhibidores de nav1.8Info
- Publication number
- AR116939A1 AR116939A1 ARP190103169A ARP190103169A AR116939A1 AR 116939 A1 AR116939 A1 AR 116939A1 AR P190103169 A ARP190103169 A AR P190103169A AR P190103169 A ARP190103169 A AR P190103169A AR 116939 A1 AR116939 A1 AR 116939A1
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- Prior art keywords
- 6alkyl
- heteroaryl
- aryl
- 6alkenyl
- group
- Prior art date
Links
- 101000654356 Homo sapiens Sodium channel protein type 10 subunit alpha Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102100031374 Sodium channel protein type 10 subunit alpha Human genes 0.000 title 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 18
- 125000001072 heteroaryl group Chemical group 0.000 abstract 17
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 150000002367 halogens Chemical class 0.000 abstract 13
- 125000003118 aryl 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 9
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 9
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- -1 cycloheteroalkyl Chemical group 0.000 abstract 5
- 150000002431 hydrogen Chemical class 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 abstract 2
- 208000002193 Pain Diseases 0.000 abstract 2
- 125000002619 bicyclic group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 206010065390 Inflammatory pain Diseases 0.000 abstract 1
- 208000003251 Pruritus Diseases 0.000 abstract 1
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 230000001154 acute effect Effects 0.000 abstract 1
- 208000005298 acute pain Diseases 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000007803 itching Effects 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 229960003966 nicotinamide Drugs 0.000 abstract 1
- 235000005152 nicotinamide Nutrition 0.000 abstract 1
- 239000011570 nicotinamide Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
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- 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
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
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- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- C07D213/00—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
- C07D213/02—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
- 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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- 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
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Abstract
Compuestos derivados de nicotinamida como inhibidores de la actividad de los canales de sodio Naᵛ1.8, composiciones farmacéuticas que los comprenden y su uso en el tratamiento o prevención del dolor, tales como el dolor agudo, dolor neuropático, dolor inflamatorio y trastornos de picazón aguda y crónica. Reivindicación 1: Un compuesto de la fórmula estructural [1], o una sal farmacéuticamente aceptable del mismo, en donde A es heteroarilo o heteroarilo fusionado con un anillo de 5 ó 6 miembros saturado o insaturado que contiene 0 - 3 heteroátomos seleccionados independientemente de O, S y N(Rʰ)q, en donde cada heteroarilo, anillo de 5 miembros y anillo de 6 miembros no está sustituido o está sustituido con uno a cinco sustituyentes seleccionados de Rᵃ; B es heteroarilo, en donde el heteroarilo no está sustituido o está sustituido con uno a tres sustituyentes seleccionados de Rᵇ; R¹ se selecciona del grupo que consiste en: (1) hidrógeno, (2) -SO₃H, (3) -SO₂NH₂, (4) -SO₂NRᵉC₁₋₆alquilo, (5) -SO₂NRᵉC(O)C₁₋₆alquilo, (6) -SO₂NRᵉC₂₋₆alquenilo, (7) -SO₂NRᵉC₃₋₆cicloalquilo, (8) -SO₂NRᵉC(O)C₃₋₆cicloalquilo, (9) -SO₂NRᵉC₂₋₆cicloheteroalquilo, (10) -SO₂NRᵉC(O)C₂₋₆cicloheteroalquilo, (11) -SO₂NRᵉ-arilo, (12) -SO₂NRᵉ-heteroarilo, (13) SO₂C₁₋₆alquilo, (14) -SO₂C₁₋₆alquenilo, (15) -SO₂C₃₋₆cicloalquilo, (16) -SO₂C₂₋₆cicloheteroalquilo, (17) -SO₂arilo, (18) -SO₂heteroarilo, (19) -S(O)Rʲ, (20) -SRʲ, (21) -C(O)NH₂, (22) -C(O)NRᵉRʲ, (23) -CO₂H, (24) -CO₂Rʲ, (25) -C(O)Rʲ, (26) -CN, (27) CF₃, (28) halógeno, (29) -OH, (30) -OC₁₋₆alquilo, (31) -OC₂₋₆alquenilo, (32) -OC₃₋₆cicloalquilo, (33) -OC₂₋₆cicloheteroalquilo, (34) -O-arilo, (35) -O-heteroarilo, (36) -OC(O)Rʲ, (37) -OC(O)NRᵉRʲ, (38) -OC(O)N(Rʲ)₂, (39) -C₁₋₆alquilo, (40) -C₂₋₆alquenilo, (41) -C₁₋₆cicloalquilo, (42) -C₂₋₆cicloheteroalquilo, (43) arilo, (44) heteroarilo, (45) -(CH₂)ₙNRᵉC(O)Rʲ, (46) -(CH₂)ₙNRᵉC(O)ORʲ, (47) -(CH₂)ₙNRᵉC(O)N(Rᵉ)₂, (48) -(CH₂)ₙNRᵉC(O)NRᵉRʲ, (49) -(CH₂)ₙNRᵉC(O)N(Rʲ)₂, (50) -(CH₂)ₙNRᵉS(O)ₘRʲ, (51) -(CH₂)ₙNRᵉS(O)ₘN(Rᵉ)₂, (52) -(CH₂)ₙNRᵉS(O)ₘNRᵉRʲ, (53) -(CH₂)ₙNRᵉS(O)ₘN(Rʲ)₂, y (54) -(CH₂)ₙNRᵉRʲ, en donde cada CH₂, alquilo, alquenilo, cicloalquilo, cicloheteroalquilo, arilo y heteroarilo no está sustituido o está sustituido con uno a cuatro sustituyentes seleccionados de Rᵈ; R² se selecciona del grupo que consiste en: (1) hidrógeno, y (2) -C₁₋₆alquilo; R³ se selecciona del grupo que consiste en: (1) un anillo de C₃₋₁₂cicloalquilo monocíclico, bicíclico o espirocíclico, y (2) un anillo de C₂₋₁₂cicloheteroalquilo monocíclico, bicíclico o espirocíclico, en donde el cicloheteroalquilo contiene 1 - 4 heteroátomos seleccionados independientemente de N(Rᵐ)ʳ, O y S, en donde cada anillo de cicloalquilo y cada anillo de cicloheteroalquilo se pueden fusionar con un arilo o heteroarilo, y en donde cada cicloalquilo, cicloheteroalquilo, arilo y heteroarilo no está sustituido o está sustituido con uno a ocho sustituyentes seleccionados de Rᶜ; cada Rᵃ se selecciona del grupo que consiste en: (1) -C₁₋₆alquilo, (2) -OC₁₋₆alquilo, (3) halógeno, (4) -OH, (5) oxo, (6) -CN, (7) -C₃₋₆cicloalquilo, y (8) -C₂₋₅cicloheteroalquilo, en donde cada alquilo, cicloalquilo y cicloheteroalquilo no está sustituido o está sustituido con uno a seis sustituyentes seleccionados de halógeno, OH, NH₂, NH(C₁₋₆alquilo) y N(C₁₋₆alquilo)₂; cada Rᵇ se selecciona independientemente del grupo que consiste en: (1) -CF₃, (2) -CF₂CF₃, (3) -CHF₂, (4) -OCHF₂, (5) -OCH₂CF₃, (6) -OCF₃, (7) CN, (8) halógeno, (9) -Si(C₁₋₆alquilo)₃, (10) -C₁₋₆alquil-O-Rᵏ, (11) -C₁₋₆alquilo, (12) -C₂₋₆alquenilo, (13) -C₂₋₆alquinilo, (14) -C₃₋₆cicloalquilo, (15) -C₂₋₆cicloheteroalquilo, (16) arilo, (17) heteroarilo, (18) -C₁₋₆alquil-C₃₋₆cicloalquilo, (19) -C₁₋₆alquil-C₂₋₆cicloheteroalquilo, (20) -C₁₋₆alquil-arilo, (21) -C₁₋₆alquil-heteroarilo, (22) C₂₋₆alquenil-C₃₋₆cicloalquilo, (23) -C₂₋₆alquenil-C₂₋₆cicloheteroalquilo, (24) -C₂₋₆alquenil-arilo, (25) -C₂₋₆alquenil-heteroarilo, (26) -C₂₋₆alquinil-C₃₋₆cicloalquilo, (27) -C₂₋₆alquinil-cicloheteroalquilo, (28) -C₂₋₆alquinil-arilo, (29) -C₂₋₆alquinil-heteroarilo, (30) NO₂, (31) -OH, (32) -(CH₂)ₚ-OC₁₋₆alquilo, (33) -(CH₂)ₚ-OC₂₋₆alquenilo, (34) -(CH₂)ₚ-OC₂₋₆alquinilo, (35) -(CH₂)ₚ-OC₃₋₆cicloalquilo, (36) -(CH₂)ₚ-OC₂₋₆heterocicloalquilo, (37) -(CH₂)ₚ-O-arilo, (38) -(CH₂)ₚ-O-heteroarilo, (39) -OC₁₋₆alquil-C₃₋₆cicloalquilo, (40) -OC₁₋₆alquil-C₂₋₆heterocicloalquilo, (41) -OC₁₋₆alquil-arilo, (42) -OC₁₋₆alquil-heteroarilo, (1) -S(O)ₘRᵏ, (43) -C₁₋₆alquil-S(O)ₘRᵏ, (44) -C(O)Rᵏ, (45) -N(Rⁱ)₂, y (46) -NRⁱRᵏ, en donde cada Rᵇ no está sustituido o está sustituido con uno a cinco sustituyentes seleccionados de Rᶠ; cada Rᶜ se selecciona independientemente del grupo que consiste en: (1) -CF₃, (2) -CH₂CF₃, (3) -CHF₂, (4) -OCHF₂, (5) -OCF₃, (6) CN, (7) oxo, (8) -OH, (9) halógeno, (10) -C₁₋₆alquilo, (11) -C₂₋₆alquenilo, (12) -C₂₋₆alquinilo, (13) -C₃₋₆cicloalquilo, (14) -C₂₋₆cicloheteroalquilo, (15) -C₁₋₆alquil-C₃₋₆cicloalquilo, (16) -C₁₋₆alquil-C₂₋₆cicloheteroalquilo, (17) -C₁₋₆alquil-arilo, (18) -C₁₋₆alquil-heteroarilo, (19) -C₁₋₆alquenil-C₃₋₆cicloalquilo, (20) -C₁₋₆alquenil-arilo, (21) -C₁₋₆alquenil-heteroarilo, (22) -C₁₋₆alquenil-C₂₋₆cicloheteroalquilo, (23) -C₂₋₆alquinil-C₃₋₆cicloalquilo, (24) -C₂₋₆alquinil-C₂₋₆cicloheteroalquilo, (25) -C₂₋₆alquinil-arilo, (26) -C₂₋₆alquinil-heteroarilo, (27) -OC₁₋₆alquilo, (28) -OC₂₋₆alquenilo, (29) -OC₂₋₆alquinilo, (30) -OC₃₋₆cicloalquilo, (31) -OC₂₋₆heterocicloalquilo, (32) -O-arilo, (33) -O-heteroarilo, (34) -OC₁₋₆alquil-cicloalquilo, (35) -OC₁₋₆alquil-cicloheteroalquilo, (36) -OC₁₋₆alquil-arilo, (37) -OC₁₋₆alquil-heteroarilo, (38) -S(O)ₘRL, (39) -S(O)RL, (40) -S-RL, (41) -C₁₋₆alquil-S(O)ₘRL, (42) -C(O)RL, (43) -C(O)C₁₋₆alquil-RL, (44) -OC(O)RL, (45) -CO₂RL, (46) arilo, y (47) heteroarilo, en donde cada Rᶜ no está sustituido o está sustituido con uno a cinco sustituyentes seleccionados de Rᵍ; Rᵈ se selecciona independientemente del grupo que consiste en: (1) hidrógeno, (2) halógeno, (3) OH, (4) oxo, (5) -C₁₋₆alquilo, (6) -OC₁₋₆alquilo, (7) NH₂, (8) NH(C₁₋₆alquilo), y (9) N(C₁₋₆alquilo)₂; cada Rᵉ se selecciona independientemente del grupo que consiste en: (1) hidrógeno, y (2) -C₁₋₆alquilo; cada Rᶠ se selecciona del grupo que consiste en: (1) halógeno, F, (2) -C₁₋₆alquilo, (3) -OH, (4) -OC₁₋₆alquilo, (5) -OC₃₋₆cicloalquilo, (6) -OC₂₋₆cicloheteroalquilo, (7) CN, (8) -NH₂, (9) -NH(C₁₋₆alquilo), (10) -NH(C₃₋₆cicloalquilo), (11) -NH(C₂₋₆cicloheteroalquilo), (12) -N(C₁₋₆alquilo)₂, (13) -N(C₃₋₆cicloalquilo)₂, y (14) -N(C₂₋₆cicloheteroalquilo)₂, en donde cada alquilo, cicloalquilo y cicloheteroalquilo no está sustituido o está sustituido con uno a tres sustituyentes seleccionados independientemente de: -OH, halógeno, ciano y -S(O)₂CH₃; cada Rᵍ se selecciona del grupo que consiste en: (1) halógeno, (2) C₁₋₆alquilo, (3) -OH, (4) -OC₁₋₆alquilo, (5) -S(O)ₘ-C₁₋₆alquilo, (6) -CN, (7) -CF₃, (8) -OCHF₂, y (9) -OCF₃, en donde cada alquilo no está sustituido o está sustituido con uno a tres sustituyentes seleccionados independientemente de: -OH, halógeno, ciano y -S(O)₂CH₃; cada Rʰ se selecciona independientemente del grupo que consiste en: (1) hidrógeno, y (2) -C₁₋₆alquilo; cada Rⁱ se selecciona independientemente del grupo que consiste en: (1) hidrógeno, y (2) -C₁₋₆alquilo; cada Rʲ se selecciona del grupo que consiste en: (1) -C₁₋₆alquilo, (2) -C₂₋₆alquenilo, (3) -C₃₋₆cicloalquilo, (4) -C₂₋₆cicloheteroalquilo, (5) arilo, y (6) heteroarilo, en donde cada alquilo, alquenilo, cicloalquilo, cicloheteroalquilo, arilo y heteroarilo no está sustituido o está sustituido con uno a tres sustituyentes seleccionados independientemente de: -C₁₋₆alquilo, -C₃₋₆cicloalquilo, -OH, -OC₁₋₆alquilo, -OC₃₋₆cicloalquilo, halógeno, ciano y -S(O)₂CH₃; cada Rᵏ se selecciona del grupo que consiste en: (1) -C₁₋₆alquilo, (2) -C₂₋₆alquenilo, (3) -C₃₋₆cicloalquilo, (4) -C₃₋₆cicloalquilo, (5) -C₂₋₆cicloheteroalquilo, (6) arilo, y (7) heteroarilo, en donde cada alquilo, alquenilo, cicloalquilo, cicloheteroalquilo, arilo y heteroarilo no está sustituido o está sustituido con uno a tres sustituyentes seleccionados independientemente de: -C₁₋₆alquilo, -C₃₋₆cicloalquilo, -OH, -OC₁₋₆alquilo, -OC₃₋₆cicloalquilo, halógeno, ciano y - S(O)₂CH₃; cada RL se selecciona del grupo que consiste en: (1) -C₁₋₆alquilo, (2) -C₂₋₆alquenilo, (3) -C₃₋₆cicloalquilo, (4) -C₂₋₆cicloheteroalquilo, (5) arilo, y (6) heteroarilo, en donde cada alquilo, alquenilo, cicloalquilo, cicloheteroalquilo, arilo y heteroarilo no está sustituido o está sustituido con uno a tres sustituyentes seleccionados independientemente de: -C₁₋₆alquilo, -C₃₋₆cicloalquilo, -OH, -OC₁₋₆alquilo, -OC₃₋₆cicloalquilo, halógeno, ciano y -S(O)₂CH₃; cada Rᵐ se selecciona independientemente del grupo que consiste en: (1) hidrógeno, y (2) -C₁₋₆alquilo; cada n es independientemente 0, 1, 2, 3 ó 4; cada m es independientemente 0, 1 ó 2; cada p es independientemente 0, 1, 2, 3 ó 4; cada q es independientemente 0 ó 1; y cada r es independientemente 0 ó 1.
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