AR070207A1 - Derivados biciclicos de carboxamidas aza- biciclicas su preparacion y su aplicacion terapeutica - Google Patents
Derivados biciclicos de carboxamidas aza- biciclicas su preparacion y su aplicacion terapeuticaInfo
- Publication number
- AR070207A1 AR070207A1 ARP090100167A ARP090100167A AR070207A1 AR 070207 A1 AR070207 A1 AR 070207A1 AR P090100167 A ARP090100167 A AR P090100167A AR P090100167 A ARP090100167 A AR P090100167A AR 070207 A1 AR070207 A1 AR 070207A1
- Authority
- AR
- Argentina
- Prior art keywords
- cycloalkyl
- alkylene
- alkyl
- aryl
- group
- Prior art date
Links
- 230000001225 therapeutic effect Effects 0.000 title 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 32
- 125000002947 alkylene group Chemical group 0.000 abstract 23
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 19
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000003118 aryl group Chemical group 0.000 abstract 15
- 125000001072 heteroaryl group Chemical group 0.000 abstract 11
- 229910052757 nitrogen Inorganic materials 0.000 abstract 11
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 10
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 abstract 10
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 10
- -1 C 1-6 fluoroalkylene Chemical group 0.000 abstract 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 8
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000004428 fluoroalkoxy group Chemical group 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 150000003573 thiols Chemical class 0.000 abstract 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- 229940079593 drug Drugs 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 abstract 2
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical group C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 abstract 1
- 108010025083 TRPV1 receptor Proteins 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000005529 alkyleneoxy group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 abstract 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000003951 lactams Chemical class 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P11/00—Drugs for disorders of the respiratory system
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/14—Decongestants or antiallergics
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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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- 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
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
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- Communicable Diseases (AREA)
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- Pain & Pain Management (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Procedimiento de preparacion, medicamento, composicion farmacéutica y uso para preparar medicamento para prevenir o tratar enfermedades donde están implicados receptores TRPV1. Reivindicacion 1: Compuesto que responde a la formula (1) en la que X1, X2, X3 y X4 representan, independientemente uno del otro, un átomo de nitrogeno o un grupo C-R1; entendiéndose que cuando uno de X1, X2, X3 y X4 representa un átomo de nitrogeno, los otros representan un grupo C-R1; W representa un átomo de O o de S; n es igual a 0, 1, 2 o 3; Y representa un arilo o un heteroarilo sustituido opcionalmente con uno o varios grupos seleccionados entre un átomo de halogeno, un grupo alquilo C1-6, cicloalquilo 3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquileno C1-6, hidroxi, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-6-O-, fluoroalcoxi C1-6, ciano, C(O)NR4R5, nitro, NR4R5, tioalquilo C1-6, tiol, -S(O)-alquilo C1-6, -S(O)2-alquilo C1-6, SO2NR4R5, NR6C(O)R7, NR6SO2R8, C(O)NR4R5, OC(O)NR4R5, -Si-(alquilo C1-6)3, -SF5, arilo-alquileno C1-5 o arilo, heteroaril-alquileno C1-5 o heteroarilo; estando los grupos alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquileno C1-6-O- sustituidos opcionalmente con un grupo hidroxi, alcoxi C1-6 o NR4R5, los grupos arilo y heteroarilo están, opcionalmente sustituidos con uno o varios sustituyentes R9 idénticos o diferentes el uno del otro; A representa el grupo de la formula (2), Z1, Z2, Z3 y Z4 representan, independientemente el uno del otro, un átomo de nitrogeno, un átomo de carbono o un grupo C-R2, uno, al menos, de Z1, Z2, Z3 y Z4 corresponde a un átomo de nitrogeno y uno de Z1, Z2, Z3 y Z4, que corresponde a un átomo de carbono, esta unido al átomo de nitrogeno de la amida o de la tioamida de la formula (1); Ra y Rb forman junto con los átomos de carbono a los que están unidos, bien un cicloalquilo parcialmente insaturado, o un arilo; o un heterociclo, o un heteroarilo de 5 a 7 miembros que comprende de 1 a 3 heteroátomos seleccionados de O, S o N; entendiéndose que cuando Ra y Rb forman, junto con los átomos de C a los que están unidos, un ciclo de 5 miembros, se excluye el ciclo que comprende un átomo de N y átomos de C, estando dicho ciclo parcialmente saturado o insaturado; pudiendo estar sustituido este cicloalquilo parcialmente insaturado, este arilo, este heterociclo o este heteroarilo con uno o varios sustituyentes R3; R1 se selecciona entre un átomo de hidrogeno, un átomo de halogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, ariloxi-alquilo C1-6, heteroariloxi-alquilo C1-6, aril-alquilen C1-3-oxi-alquilo C1-6, heteroaril-alquilen C1-3-oxi-alquilo C1-6, ariltio-alquilo C1-6, heteroariltio-alquilo C1-6, aril-alquilen C1-3-tio-alquilo C1-6, heteroaril-alquilen C1-3-tio-alquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi, fluoroalcoxi C1-6, ciano, C(O)NR4R5, nitro, NR4R5, tioalquilo C1-6, cicloalquil C3-7-tio, cicloalquil C3-7-alquilen C1-3-tio, -S(O)-alquilo C1-6, -S(O)-cicloalquilo C3-7, -S(O)-alquilen C1-3-cicloalquilo C3-7, alquil C1-6-S(O)2-, fluoroalquiI C1-6-S(O)2-, cicIoalquil C3-7-S(O)2-, cicloalquil C3-7-alquilen C1-3-S(O)2-, SO2NR4R5, -Si-(alquil C1-6)3, SF5, NR6C(O)R7, NR6SO2R8, C(O)NR4R5, OC(O)NR4R5, arilo, heteroarilo, aril-alquileno C1-5, heteroaril-alquileno C1-5, ariloxi, ariltio, heteroariloxi o heteroariltio; estando los grupos heteroarilo o arilo opcionalmente sustituidos con uno o varios sustituyentes R9, que son idénticos o diferentes uno del otro; R2 representa un átomo de hidrogeno, un átomo de halogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi-, hidroxi, tiol, fluoroalcoxi C1-6; R3, representa, cuando está unido a un átomo de carbono, un átomo de hidrogeno, un grupo hidroxi, tiol, alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi; alcoxi C1-6-alquileno C1-3, cicloalquil C3-7-oxi-alquileno C1-3, cicloalquil C3-7-alquilen C1-3-oxi-alquileno C1-3, C(O)NR4R5, C(O)O-alquilo C1-6, CO2H, oxo, tio; los grupos alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi, alcoxi C1-6-alquileno C1-3, cicloalquil C3-7-oxi-alquileno C1-3, cicloalquil C3-7-alquilen C1-3-oxi-alquileno C1-3 pueden estar sustituidos con un grupo hidroxi, alcoxi C1-6, -OC(O)-alquilo C1-6 o NR4R5; o R3, representa, cuando está unido a un átomo de nitrogeno, un átomo de hidrogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, arilo-C(O)-, alquil C1-6-C(O)-, cicloalquil C3-7-C(O)-, cicloalquil C3-7-alquilen C1-3-C(O)-, fluoroalquil C1-6-C(O)-, aril-S(O), alquil C1-6-S(O)-, fluoroalquil C1-6-S(O)-, aril-S(O)2-, alquilo C1-6-S(O)2-, fluoroalquil C1-6-S(O)2-, cicloalquil C3-7-S(O)2, cicloalquil C3-7-alquilen C1-3-S(O)2-, alquil C1-6-O-C(O)-, aril-alquilo C1-3-O-C(O)-, cicloalquil C3-7-O-C(O)-, cicloalquil C3-7-alquilen C1-3-O-C(O)-, fluoroalquil C1-6-O-C(O)-, aril-O-C(O)-, heteroaril-O-C(O)-, heteroarilo o arilo; los grupos heteroarilo o arilo están sustituidos, opcionalmente, con uno o varios sustituyentes R9; idénticos o diferentes uno del otro; los grupos alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, pueden estar sustituidos con un grupo hidroxi, alcoxi C1-6 o NR4R5; R4 y R5, representan, independientemente el uno del otro, un átomo de hidrogeno o un grupo alquilo C1-6, cicloalquilo C3-7, cicIoalquil C3-7-alquileno C1-3, aril-alquileno C1-5 o arilo, o R4 y R5 forman, junto con el átomo de nitrogeno al que están unidos un grupo azetidina, pirrolidina, piperidina, azepina, morfolina, tiomorfolina, piperazina, homopiperazina; estando el grupo NR4R5 opcionalmente sustituido con un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, aril-alquileno C 1-6, arilo, heteroarilo, aril-S(O)2, aIquil C1-6-S(O)2-, fluoroalquil C1-6-S(O)2, cicloalquil C3-7-S(O)2-, cicloalquil C3-7-alquilen C1-3-S(O)2-, aril-C(O)-, alquil C1-6-C(O)-, cicloalquil C3-7-C(O)-, cicloalquil C3-7-alquilen C1-3-C(O)-, fluoroalquil C1-6-C(O)-, hidroxi, alquil C1-6-oxi, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi, fluoroalquilo C1-6, ariloxi-alquileno C1-6, ariloxi, heteroariloxi-alquileno C1-6, heteroariloxi; R6 y R7 representan, independientemente el uno del otro, un átomo de hidrogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, aril-alquileno C1-6 o arilo; estando el grupo arilo opcionalmente sustituido con uno o varios sustituyentes seleccionados entre un átomo de halogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi, fluoroalcoxi C1-6, nitro o ciano; o R6 y R7 juntos forman una lactama de 4 a 7 miembros que comprende el átomo de nitrogeno y el grupo C(O) al que están unidos; R8 representa un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, aril-alquileno C1-6 o arilo; estando el grupo arilo opcionalmente sustituido con uno o varios sustituyentes seleccionados entre un átomo de halogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi, fluoroalcoxi C1-6, nitro o ciano; o R6 y R8 juntos forman una sultama de 4 a 7 miembros que comprende el átomo de nitrogeno y el grupo S(O)2 al que están unidos; R9 representa un átomo de halogeno, un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquil-C3-7-alquileno C1-3, fluoroalquilo C1-6, alcoxi C1-6, cicloalquil C3-7-oxi, cicloalquil C3-7-alquilen C1-3-oxi, fluoroalcoxi C1-6; estos grupos están sustituidos opcionalmente con un grupo OH, alcoxi C1-6 o NR4R5 o R9 representa un grupo nitro, ciano o NR4R5; pudiendo estar el o los átomos de azufre del compuesto de la formula general (1) en forma oxidada; pudiendo estar el o los átomos de nitrogeno del compuesto de la formula general (1) en forma oxidada; en forma de base o de sal de adicion a un ácido, así como en forma de hidrato o de solvato. Reivindicacion 13: Compuesto de la formula general (2A), (2B), (2C), (2D), (2E), (2F), (2G) o (2H).
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| FR2926554B1 (fr) * | 2008-01-22 | 2010-03-12 | Sanofi Aventis | Derives de carboxamides azabicycliques, leur preparation et leur application en therapeutique |
| JP5977837B2 (ja) | 2011-12-21 | 2016-08-24 | ノヴィラ・セラピューティクス・インコーポレイテッド | B型肝炎抗ウイルス剤 |
| NZ743463A (en) | 2012-08-28 | 2019-09-27 | Janssen Sciences Ireland Uc | Sulfamoyl-arylamides and the use thereof as medicaments for the treatment of hepatitis b |
| MX366123B (es) | 2013-02-28 | 2019-06-27 | Janssen Sciences Ireland Uc | Sulfamoil-arilamidas y el uso de las mismas como medicamentos para el tratamiento de la hepatitis b. |
| EA027068B1 (ru) | 2013-04-03 | 2017-06-30 | Янссен Сайенсиз Айрлэнд Юси | Производные n-фенилкарбоксамида и их применение в качестве лекарственных препаратов для лечения гепатита b |
| JO3603B1 (ar) | 2013-05-17 | 2020-07-05 | Janssen Sciences Ireland Uc | مشتقات سلفامويل بيرولاميد واستخدامها كادوية لمعالجة التهاب الكبد نوع بي |
| CN105960400B (zh) | 2013-05-17 | 2019-05-31 | 爱尔兰詹森科学公司 | 氨磺酰基噻吩酰胺衍生物及其作为药物用于治疗乙型肝炎的用途 |
| PL3024819T3 (pl) | 2013-07-25 | 2018-08-31 | Janssen Sciences Ireland Uc | Pochodne piroloamidowe podstawione glioksamidem i ich zastosowanie jako leków do leczenia wirusowego zapalenia wątroby typu B |
| EP3060547B1 (en) | 2013-10-23 | 2017-10-11 | Janssen Sciences Ireland UC | Carboxamide derivatives and the use thereof as medicaments for the treatment of hepatitis b |
| US10392349B2 (en) | 2014-01-16 | 2019-08-27 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| US9169212B2 (en) | 2014-01-16 | 2015-10-27 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| US20150216938A1 (en) | 2014-02-05 | 2015-08-06 | Novira Therapeutics Inc. | Combination therapy for treatment of hbv infections |
| CN110483484A (zh) | 2014-02-06 | 2019-11-22 | 爱尔兰詹森科学公司 | 氨磺酰基吡咯酰胺衍生物及其作为药物用于治疗乙型肝炎的用途 |
| CN107847762A (zh) | 2015-03-19 | 2018-03-27 | 诺维拉治疗公司 | 氮杂环辛烷和氮杂环壬烷衍生物以及治疗乙型肝炎感染的方法 |
| US10875876B2 (en) | 2015-07-02 | 2020-12-29 | Janssen Sciences Ireland Uc | Cyclized sulfamoylarylamide derivatives and the use thereof as medicaments for the treatment of hepatitis B |
| HK1259410A1 (zh) | 2015-09-29 | 2019-11-29 | 诺维拉治疗公司 | 乙型肝炎抗病毒剂的晶体形式 |
| CN109640980A (zh) | 2016-04-15 | 2019-04-16 | 诺维拉治疗公司 | 包含壳体装配抑制剂的组合和方法 |
| ES2747768T3 (es) | 2017-03-20 | 2020-03-11 | Forma Therapeutics Inc | Composiciones de pirrolopirrol como activadores de quinasa de piruvato (PKR) |
| CA3090125A1 (en) | 2018-03-14 | 2019-09-19 | Janssen Sciences Ireland Unlimited Company | Capsid assembly modulator dosing regimen |
| WO2020061255A1 (en) | 2018-09-19 | 2020-03-26 | Forma Therapeutics, Inc. | Activating pyruvate kinase r |
| WO2020061378A1 (en) | 2018-09-19 | 2020-03-26 | Forma Therapeutics, Inc. | Treating sickle cell disease with a pyruvate kinase r activating compound |
| JP2022521081A (ja) | 2019-02-22 | 2022-04-05 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | Hbv感染若しくはhbv誘導性疾患の治療において有用なアミド誘導体 |
| MA55879A (fr) | 2019-05-06 | 2022-03-16 | Janssen Sciences Ireland Unlimited Co | Dérivés d'amide utiles dans le traitement d'une infection par le virus de l'hépatite b ou de maladies induites par le virus de l'hépatite b |
| US20220378756A1 (en) | 2019-09-19 | 2022-12-01 | Forma Therapeutics, Inc. | Activating pyruvate kinase r |
| US12128035B2 (en) | 2021-03-19 | 2024-10-29 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
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| FR2874015B1 (fr) * | 2004-08-05 | 2006-09-15 | Sanofi Synthelabo | Derives de n-(1h-indolyl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique |
| JP2006072736A (ja) * | 2004-09-02 | 2006-03-16 | Canon Inc | 情報処理装置及び方法及びプログラム及び記憶媒体 |
| WO2006072735A1 (fr) | 2005-01-05 | 2006-07-13 | Palga International | Procede et installation de fabrication d'un produit alimentaire de forme allongee a l'aide d'un dispositif de restriction et produit alimentaire obtenu |
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| FR2897061B1 (fr) * | 2006-02-03 | 2010-09-03 | Sanofi Aventis | Derives de n-heteroaryl-carboxamides tricycliques contenant un motif benzimidazole, leur preparation et leur application en therapeutique. |
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| FR2926554B1 (fr) * | 2008-01-22 | 2010-03-12 | Sanofi Aventis | Derives de carboxamides azabicycliques, leur preparation et leur application en therapeutique |
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