AR036876A1 - HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM - Google Patents
HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEMInfo
- Publication number
- AR036876A1 AR036876A1 ARP020103521A ARP020103521A AR036876A1 AR 036876 A1 AR036876 A1 AR 036876A1 AR P020103521 A ARP020103521 A AR P020103521A AR P020103521 A ARP020103521 A AR P020103521A AR 036876 A1 AR036876 A1 AR 036876A1
- Authority
- AR
- Argentina
- Prior art keywords
- branched
- linear
- group
- groups
- alkyl
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 239000001301 oxygen Substances 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- -1 hydroxy, amino Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 239000011593 sulfur Substances 0.000 abstract 3
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- 238000011282 treatment Methods 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 230000001419 dependent effect Effects 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 208000035475 disorder Diseases 0.000 abstract 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 208000001072 type 2 diabetes mellitus Diseases 0.000 abstract 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- MQCMONHCZPPVEK-UHFFFAOYSA-N 6-benzoyl-3-[2-[4-[(2-oxo-1,3-dihydroindol-3-yl)methyl]phenoxy]ethyl]-1,3-benzothiazol-2-one Chemical group C=1C=C2N(CCOC=3C=CC(CC4C5=CC=CC=C5NC4=O)=CC=3)C(=O)SC2=CC=1C(=O)C1=CC=CC=C1 MQCMONHCZPPVEK-UHFFFAOYSA-N 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 241000234282 Allium Species 0.000 abstract 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 abstract 1
- 208000000103 Anorexia Nervosa Diseases 0.000 abstract 1
- 206010003210 Arteriosclerosis Diseases 0.000 abstract 1
- 206010006187 Breast cancer Diseases 0.000 abstract 1
- 208000026310 Breast neoplasm Diseases 0.000 abstract 1
- 208000032841 Bulimia Diseases 0.000 abstract 1
- 206010006550 Bulimia nervosa Diseases 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 206010009944 Colon cancer Diseases 0.000 abstract 1
- 206010012289 Dementia Diseases 0.000 abstract 1
- 208000032928 Dyslipidaemia Diseases 0.000 abstract 1
- 208000002705 Glucose Intolerance Diseases 0.000 abstract 1
- 206010018429 Glucose tolerance impaired Diseases 0.000 abstract 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 abstract 1
- 102000004877 Insulin Human genes 0.000 abstract 1
- 108090001061 Insulin Proteins 0.000 abstract 1
- 206010022489 Insulin Resistance Diseases 0.000 abstract 1
- 206010068871 Myotonic dystrophy Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 206010033645 Pancreatitis Diseases 0.000 abstract 1
- 201000004681 Psoriasis Diseases 0.000 abstract 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 abstract 1
- 206010048214 Xanthoma Diseases 0.000 abstract 1
- 206010048215 Xanthomatosis Diseases 0.000 abstract 1
- 230000004913 activation Effects 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 229940121369 angiogenesis inhibitor Drugs 0.000 abstract 1
- 239000004037 angiogenesis inhibitor Substances 0.000 abstract 1
- 208000022531 anorexia Diseases 0.000 abstract 1
- 230000036528 appetite Effects 0.000 abstract 1
- 235000019789 appetite Nutrition 0.000 abstract 1
- 208000011775 arteriosclerosis disease Diseases 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 150000001555 benzenes Chemical class 0.000 abstract 1
- 125000006267 biphenyl 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
- 208000029742 colonic neoplasm Diseases 0.000 abstract 1
- 208000029078 coronary artery disease Diseases 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 206010061428 decreased appetite Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 210000002889 endothelial cell Anatomy 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 abstract 1
- 229940088597 hormone Drugs 0.000 abstract 1
- 239000005556 hormone Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 201000001421 hyperglycemia Diseases 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- 229940125396 insulin Drugs 0.000 abstract 1
- 208000017169 kidney disease Diseases 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004957 naphthylene group Chemical group 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 230000007170 pathology Effects 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 201000010065 polycystic ovary syndrome Diseases 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 150000003222 pyridines Chemical class 0.000 abstract 1
- 208000011580 syndromic disease Diseases 0.000 abstract 1
- 125000000464 thioxo group Chemical group S=* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicación 1: Compuestos de la fórmula (1) en la cual: X representa un átomo de oxígeno o de azufre, un grupo CH2 ó CHR'2 (en el cual R'2 forma con R2 una enlace suplementario); Y representa un átomo de oxígeno ó de azufre, R1 y R2, idénticos o diferentes representan un átomo de hidrógeno, un grupo alquilo (C1-6) lineal o ramificado, arilo, arilalquilo (C1-6) lineal o ramificado, ariloxi, arilalquiloxi (C1-6) lineal o ramificado, alcoxi (C1-6) lineal o ramificado, hidroxi, amino, alquilamino (C1-6) lineal o ramificado ó dialquilamino (C1-6) lineal o ramificado, ó R1 y R2 forman juntos un grupo oxo, tioxo ó imino, R2 puede además formar con R'2 un enlace suplementario; A representa una cadena alquileno (C1-6) en la cual uno de sus grupos CH2 puede estar reemplazado por un heteroátomo elegido entre oxígeno o azufre, o por un grupo NRn (donde Rn representa un átomo de hidrógeno ó un grupo alquilo (C1-6) lineal o ramificado), ó por un grupo fenileno ó naftileno, B representa un grupo alquilo (C1-6) lineal o ramificado, ó alquenilo (C2-6) lineal o ramificado, ó alquinileno (C2-6) lineal o ramificado; D y D', idénticos o diferentes, representan un núcleo bencénico ó un núcleo piridínico, esos núcleos son no sustituidos o sustituidos por 1 a 3 grupos, idénticos o diferentes elegidos entre un átomo de halógeno y un grupo ciano, nitro, R, OR, S(O)nR, C(Z)R, -CH(OR)-R', C(Z)OR, NRR', C(Z)NRR', -C(=N-OR')R, -NR-C(Z)R', -NR-C(Z)OR' ó OC(Me)2COOR, (donde R y R' idénticos o diferentes representan un átomo de hidrógeno ó un grupo alquilo (C1-6) lineal o ramificado, alquenilo (C2-6) lineal o ramificado, alquinilo (C2-6) lineal o ramificado, arilo, arilalquilo (C1-6) lineal o ramificado, heteroarilo, heteroarilalquilo (C1-6) lineal o ramificado, cicloalquilo (C3-8) ó cicloalquil (C3-8)-alquilo (C1-6) lineal o ramificado; Z representa un átomo de oxígeno ó de azufre y n representa un número entero comprendido entre 0 y 2 inclusive); R3 y R4, idénticos o diferentes, representan un átomo de hidrógeno, de halógeno, un grupo R, OR ó NRR' (donde R y R' son tal como se los ha definido precedentemente), ó R3 y R4 forman junto con los átomos de carbono que los llevan, cuando son llevados por dos átomos de carbono adyacentes, un ciclo que presenta 5 ó 6 eslabones y que pueden contener un heteroátomo elegido entre oxígeno, azufre y nitrógeno; R5 representa un átomo de hidrógeno, un grupo alquilo (C1-6) lineal o ramificado, alquenilo (C2-6) lineal o ramificado, alquinilo (C2-6) lineal o ramificado, arilo, heteroarilo, alquilcarbonilo (C1-6), arilcarbonilo, ó heteroarilcarbonilo, siendo eventualmente sustituido cada uno de esos grupos: -por uno ó varios grupos R6 tal como R6 representa un grupo -(CH2)t-C(=Z)Z' (donde Z es tal como se ha definido precedentemente, Z' representa un grupo OR ó NRR' con R y R' tal como se los ha definido precedentemente y t es un entero comprendido entre 0 y 6 inclusive); -por un grupo de fórmula (2), en la cual la línea punteada significa que el enlace es simple ó doble y R7 y R8, idénticos o diferentes, representan un grupo -C(=Z)Z' (donde Z y Z' son tal como se los ha definido precedentemente), ó -por un átomo de halógeno, un grupo hidroxi, nitro, ciano, amino ó alcoxi (C1-6) lineal o ramificado, y se entiende que, salvo indicación en contrario: se entiende por arilo, un grupo fenilo, naftilo ó bifenilo, esos grupos pueden estar parcialmente hidrogenados; se entiende por heteroarilo, cualquier grupo aromático mono ó bicíclico que contiene de 5 a 10 eslabones, que puede ser parcialmente hidrogenado en uno de los ciclos en el caso de los heteroarilos bicíclicos, y que contienen 1 a 3 heteroátomos elegidos entre oxígeno, nitrógeno y azufre, los grupos arilo y heteroarilo pueden ser eventualmente sustituidos por 1 a 3 átomos de halógeno ó grupos alquilo (C1-6) lineal o ramificado, alcoxi (C1-6) lineal o ramificado, carboxi, formilo, amino, alquilamino (C1-6) lineal o ramificado, dialquilamino (C1-6) lineal o ramificado, éster, amido, nitro, ciano, y O-C(Me)2COOR (donde R es tal como se ha definido precedentemente), sus enantiómeros y diastereoisómeros así como sus sales de adición con un ácido o con una base farmacéuticamente aceptables. Reivindicación 9: Compuestos de fórmula (1) de acuerdo con una cualquiera de las reivindicaciones 1 a 8, caracterizados porque es la 3-(2-{4-[(5-benzoil-2-oxo-2,3-dihidro-1H-indol-3-il)metil]fenoxi}etil)-1,3-benzotiazol-2(3H)-ona, así como sus sales de adición con un ácido farmacéuticamente aceptable. Reivindicación 10: Compuestos de fórmula (1) de acuerdo con una cualquiera de las reivindicaciones 1 a 8, caracterizados porque es la 6-benzoil-3-(2-{4-[(2-oxo-2,3-dihidro-1H-indol-3-il)metil]fenoxi}etil)-1,3-benzotiazol-2(3H)-ona, así como sus sales de adición con un ácido farmacéuticamente aceptable. Reivindicación 13: Composiciones farmacéuticas de acuerdo con la reivindicación 12, caracterizadas porque son útiles para la fabricación de un medicamento para el tratamiento y/o profilaxis de las hiperglucemias, de las dislipidemias y más particularmente en el tratamiento de las diabetes no insulinodependientes de tipo II, de la resistencia a la insulina, de la intolerancia a la glucosa, de los desórdenes relacionados con el síndrome X, de las enfermedades arteriales coronarias y otras enfermedades cardiovasculares, de las enfermedades renales, de las retionopatías, de los desórdenes relacionados con la activación de las células endoteliales, de la psoriasis, del síndrome poliquístico de ovario, de la demencia, de la osteoporosis, de las enfermedades inflamatorias intestinales, de las distrofias miotónicas, de las pancreatitis, de la arterioesclerosis, del xantoma , pero también en el tratamiento o la prevención de la diabetes de tipo I, de la obesidad, de la regulación del apetito, de la anorexia, de la bulimia, de la anorexia nerviosa, así como de las patologías cancerosas y en especial de los cánceres hormonodependientes tales como el cáncer de pecho y el cáncer de colon y como inhibidores de angiogénesis.Claim 1: Compounds of the formula (1) in which: X represents an oxygen or sulfur atom, a CH2 or CHR'2 group (in which R'2 forms a supplementary bond with R2); Y represents an oxygen or sulfur atom, R1 and R2, identical or different, represent a hydrogen atom, a linear or branched (C1-6) alkyl group, aryl, linear or branched (C1-6) alkyl, aryloxy, arylaxyloxy (C1-6) linear or branched, linear or branched (C1-6) alkoxy, hydroxy, amino, linear or branched (C1-6) alkylamino or linear or branched (C1-6) dialkylamino, or R1 and R2 together form a oxo, thioxo or imino group, R2 can also form a supplementary bond with R'2; A represents an (C1-6) alkylene chain in which one of its CH2 groups can be replaced by a heteroatom chosen from oxygen or sulfur, or by an NRn group (where Rn represents a hydrogen atom or a (C1-) alkyl group 6) linear or branched), or by a phenylene or naphthylene group, B represents a linear or branched (C1-6) alkyl or linear or branched (C2-6) alkenyl group, or linear or branched (C2-6) alkynylene ; D and D ', identical or different, represent a benzene nucleus or a pyridine nucleus, these nuclei are unsubstituted or substituted by 1 to 3 groups, identical or different, chosen between a halogen atom and a cyano, nitro, R, OR group , S (O) nR, C (Z) R, -CH (OR) -R ', C (Z) OR, NRR', C (Z) NRR ', -C (= N-OR') R, - NR-C (Z) R ', -NR-C (Z) OR' or OC (Me) 2COOR, (where identical and different R and R 'represent a hydrogen atom or a linear (C1-6) alkyl group or branched, linear or branched (C2-6) alkenyl, linear or branched (C2-6) alkynyl, aryl, linear or branched (C1-6) arylalkyl, heteroaryl, straight or branched (C1-6) heteroarylalkyl, (C3-) cycloalkyl 8) or linear or branched (C1-6) cycloalkyl (C1-6) alkyl; Z represents an oxygen or sulfur atom and n represents an integer between 0 and 2 inclusive); R3 and R4, identical or different, represent a hydrogen atom, a halogen, a group R, OR or NRR '(where R and R' are as defined above), or R3 and R4 form together with the atoms of carbon that carry them, when they are carried by two adjacent carbon atoms, a cycle that has 5 or 6 links and can contain a heteroatom chosen from oxygen, sulfur and nitrogen; R5 represents a hydrogen atom, a linear or branched (C1-6) alkyl, linear or branched (C2-6) alkenyl, linear or branched (C2-6) alkynyl, aryl, heteroaryl, (C1-6) alkylcarbonyl group, arylcarbonyl, or heteroarylcarbonyl, each of these groups being eventually substituted: - by one or several groups R6 such as R6 represents a group - (CH2) tC (= Z) Z '(where Z is as defined above, Z 'represents an OR or NRR group' with R and R 'as defined above and t is an integer between 0 and 6 inclusive); -by a group of formula (2), in which the dotted line means that the bond is single or double and R7 and R8, identical or different, represent a group -C (= Z) Z '(where Z and Z' they are as defined above), or - by a halogen atom, a linear or branched hydroxy, nitro, cyano, amino or (C1-6) alkoxy group, and it is understood that, unless otherwise indicated: it is understood by aryl, a phenyl, naphthyl or biphenyl group, these groups may be partially hydrogenated; heteroaryl is understood as any mono or bicyclic aromatic group containing 5 to 10 links, which can be partially hydrogenated in one of the cycles in the case of bicyclic heteroaryls, and containing 1 to 3 heteroatoms chosen from oxygen, nitrogen and sulfur, the aryl and heteroaryl groups may be substituted by 1 to 3 halogen atoms or linear or branched (C1-6) alkyl groups, linear or branched (C1-6) alkoxy, carboxy, formyl, amino, (C1-) alkylamino groups 6) linear or branched, dialkylamino (C1-6) linear or branched, ester, amido, nitro, cyano, and OC (Me) 2COOR (where R is as defined above), its enantiomers and diastereoisomers as well as its salts of addition with a pharmaceutically acceptable acid or base. Claim 9: Compounds of formula (1) according to any one of claims 1 to 8, characterized in that it is 3- (2- {4 - [(5-benzoyl-2-oxo-2,3-dihydro-1H -indole-3-yl) methyl] phenoxy} ethyl) -1,3-benzothiazol-2 (3H) -one, as well as its addition salts with a pharmaceutically acceptable acid. Claim 10: Compounds of formula (1) according to any one of claims 1 to 8, characterized in that it is 6-benzoyl-3- (2- {4 - [(2-oxo-2,3-dihydro-1H -indole-3-yl) methyl] phenoxy} ethyl) -1,3-benzothiazol-2 (3H) -one, as well as its addition salts with a pharmaceutically acceptable acid. Claim 13: Pharmaceutical compositions according to claim 12, characterized in that they are useful for the manufacture of a medicament for the treatment and / or prophylaxis of hyperglycemia, of dyslipidemias and more particularly in the treatment of non-insulin-dependent type II diabetes. , insulin resistance, glucose intolerance, disorders related to syndrome X, coronary artery disease and other cardiovascular diseases, kidney diseases, rethiopathies, disorders related to activation of endothelial cells, psoriasis, polycystic ovary syndrome, dementia, osteoporosis, inflammatory bowel diseases, myotonic dystrophies, pancreatitis, arteriosclerosis, xanthoma, but also in treatment or the prevention of type I diabetes, obesity, regulation Onion of appetite, anorexia, bulimia, anorexia nervosa, as well as cancerous pathologies and especially hormone-dependent cancers such as breast cancer and colon cancer and as angiogenesis inhibitors.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0112205A FR2830012B1 (en) | 2001-09-21 | 2001-09-21 | NOVEL HETEROCYCLIC DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARAMACEUTICAL COMPOSITIONS CONTAINING THEM |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR036876A1 true AR036876A1 (en) | 2004-10-13 |
Family
ID=8867506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020103521A AR036876A1 (en) | 2001-09-21 | 2002-09-19 | HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR036876A1 (en) |
| FR (1) | FR2830012B1 (en) |
| WO (1) | WO2003027108A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2858321B1 (en) * | 2003-07-28 | 2006-01-20 | Servier Lab | NOVEL HETEROCYCLIC OXIMIC DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
| KR20050040746A (en) * | 2003-10-27 | 2005-05-03 | 주식회사 엘지생명과학 | Novel Compounds As Agonist For PPARγ And PPARα, Method For Preparation Of The Same, And Pharmaceutical Composition Containing The Same |
| DE602005013275D1 (en) * | 2004-12-02 | 2009-04-23 | Prosidion Ltd | Pyrrolopyridine-2-KARBONSÄUREAMIDE |
| FR2881137B1 (en) * | 2005-01-27 | 2007-03-02 | Servier Lab | NOVEL HETEROCYCLIC OXIMIC DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5089514A (en) * | 1990-06-14 | 1992-02-18 | Pfizer Inc. | 3-coxazolyl [phenyl, chromanyl or benzofuranyl]-2-hydroxypropionic acid derivatives and analogs as hypoglycemic agents |
| JP2002515042A (en) * | 1997-12-02 | 2002-05-21 | ドクター・レディーズ・リサーチ・ファウンデーション | Azolidinedione useful for the treatment of diabetes, dyslipidemia and hypertension, and compositions containing them |
-
2001
- 2001-09-21 FR FR0112205A patent/FR2830012B1/en not_active Expired - Fee Related
-
2002
- 2002-09-19 AR ARP020103521A patent/AR036876A1/en not_active Application Discontinuation
- 2002-09-20 WO PCT/FR2002/003213 patent/WO2003027108A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| FR2830012B1 (en) | 2003-10-31 |
| FR2830012A1 (en) | 2003-03-28 |
| WO2003027108A1 (en) | 2003-04-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CO5580746A2 (en) | DERIVATIVES OF PHENYL-PIPERAZINE AS INHIBITORS OF THE REABSORTION OF SEROTONINE | |
| ES2620634T3 (en) | Human Pyruvate Kinase Activators | |
| AR064444A1 (en) | DERIVATIVES OF AMINO-NICOTINIC AND AMINO-ISONICOTINIC ACIDS. PHARMACEUTICAL COMPOSITIONS | |
| AR037288A1 (en) | COMPOUNDS DERIVED FROM SULFONAMIDS, PROCEDURE FOR OBTAINING, PHARMACEUTICAL COMPOSITION AND USE FOR THE PREPARATION OF A MEDICINAL PRODUCT | |
| AR030048A1 (en) | HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| UY29702A1 (en) | MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS | |
| EP3331880A1 (en) | N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amine derivatives as therapeutic compounds | |
| AR061739A1 (en) | NEW NAFTALENIC DERIVATIVES, THEIR PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| AR035892A1 (en) | DERIVATIVES OF OXAZOL, PROCESS FOR PREPARATION, PHARMACEUTICAL COMPOSITIONS THAT INCLUDE THEM, AND THE USE OF SUCH COMPOUNDS IN THE PREPARATION OF MEDICINES | |
| AR078163A1 (en) | USE OF AMINODIHYDROTIAZINES FOR THE TREATMENT OR PREVENTION OF DIABETES | |
| AR043199A1 (en) | USEFUL HETEROCICLIC COMPONENTS FOR THE TREATMENT OF INFLAMMATORY AND ALLERGIC DISEASES, PROCESS FOR OPERATION AND PHARMACEUTICAL COMPOSITION CONTAINING SUCH COMPONENTS | |
| AR008829A1 (en) | DERIVATIVES 6,6- OR 6,7 SUBSTITUTED BICYCLES CONTAINING PIRIDO OR PIRIMIDO AS ANTAGONIST AGENTS FOR THE TREATMENT OF GASTROINTESTINAL, INFLAMMATORY AND CNS DISEASES, AND PHARMACEUTICAL COMPOSITION | |
| AR047056A1 (en) | DERIVATIVES OF CONDENSED PYRIMIDINS. PHARMACEUTICAL COMPOSITIONS | |
| PE20051112A1 (en) | NAPHTHYRIDINE DERIVATIVES SUBSTITUTE AS INHIBITORS OF THE INHIBITOR FACTOR OF MACROPHAGES MIGRATION | |
| AR061835A1 (en) | TETRACICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| AR057989A1 (en) | DERIVATIVES OF INDOL-2-IL-AMIDA 1,5-SUBSTITUTED. PROCESSES OF OBTAINING AND PHARMACEUTICAL COMPOSITIONS | |
| AR036876A1 (en) | HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| CY1105784T1 (en) | PIPEPAZINYLACYLPIPEPIDINE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC APPLICATION | |
| US6034246A (en) | 2-arylbenzazole compounds | |
| AR059896A1 (en) | STEREOISOMERIC DERIVATIVES OF TETRAHYDRONAFTALENE, METHOD OF PREPARATION, MEDICATIONS CONTAINING THEM, AND USE AS ANTI-INFLAMMATORY AGENTS. | |
| JP2013500946A (en) | Composition comprising thalidomide and artemisinin for the treatment of cancer | |
| DE69934027D1 (en) | 2- (N-CYANIMINO) THIAZOLIDIN-4-ON DERIVATIVES | |
| ATE290527T1 (en) | TETRAHYDROBENZINDOLE DERIVATIVES | |
| CA2475137A1 (en) | New heterocyclic oxime derivatives, their preparation process and the pharmaceutical compositions that contain them | |
| AR040605A1 (en) | PIPERAZINIL-PIPERAZINONA DERIVATIVES FOR THE TREATMENT OF DISORDERS RELATED TO THE 5-HT2A RECEIVER |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |