AR038868A1 - Derivados de 1-(2-aminoacetil)2-pirrolidincarbonitrilo, su uso para la preparacion de una formulacion farmaceutica, las formulaciones farmaceuticas que los contienen, un procedimiento para la preparacion de estos derivados, y los intermediarios y su uso en dicho procedimiento de preparacion - Google Patents
Derivados de 1-(2-aminoacetil)2-pirrolidincarbonitrilo, su uso para la preparacion de una formulacion farmaceutica, las formulaciones farmaceuticas que los contienen, un procedimiento para la preparacion de estos derivados, y los intermediarios y su uso en dicho procedimiento de preparacionInfo
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- AR038868A1 AR038868A1 ARP030100723A ARP030100723A AR038868A1 AR 038868 A1 AR038868 A1 AR 038868A1 AR P030100723 A ARP030100723 A AR P030100723A AR P030100723 A ARP030100723 A AR P030100723A AR 038868 A1 AR038868 A1 AR 038868A1
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- 239000008194 pharmaceutical composition Substances 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 5
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 abstract 3
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- -1 nitro, cyano, amino Chemical group 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- XDOMURQNGATABE-UHFFFAOYSA-N 1-(2-aminoacetyl)pyrrolidine-2-carbonitrile Chemical class NCC(=O)N1CCCC1C#N XDOMURQNGATABE-UHFFFAOYSA-N 0.000 abstract 1
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002255 enzymatic effect Effects 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000004306 triazinyl group Chemical group 0.000 abstract 1
Classifications
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- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
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Abstract
Derivados de 1-(2-aminoacetil)-2-pirrolidincarbonitrilo, de fórmula general (1), en donde: R1 significa una unidad aromática que contiene N que consiste en uno o dos anillos aromáticos, preferiblemente anillo(s) piridilo, piridazinilo, pirimidinilo, pirazinilo, imidazolilo, pirazolilo, tiazolilo, isotiazolilo, oxazolilo, isoxazolilo, oxadiazolilo, quinolinilo, isoquinolinilo, cinolinilo, ftalazinilo, quinazolinilo, quinoxalinilo, benzimidazolilo, indazolilo, benzotiazolilo, benzisotiazolilo, benzoxazolilo o benzisoxazolilo, tetrazolilo, triazinilo; que en un caso determinado, está(n) mono- o disustituido(s) independientemente uno del otro por uno o dos de los siguientes grupos: grupos alquilo C1-4, alcoxi C1-4, átomo de halógeno, grupo trihalogenometilo, grupo metiltio, grupo nitro, ciano, amino o fenilo; o un grupo tienilo, furilo o bencilo; o un grupo p-toluensulfonilo; o un grupo acilo de fórmula R1a-CO, donde R1a significa un grupo alquilo C1-4, grupo fenilo; grupo fenilo, piridilo o feniletenilo sustituido con uno o más grupo(s) alquilo y/o alcoxi o nitro o átomo de halógeno, grupo feniletenilo o feniletilo sustituido con un grupo alquilendioxi; grupo piperidin-1-ilo, 4-metilpiperazin-1-ilo, pirrolidin-1-ilo, B representa un resto seleccionado del grupo de fórmulas (2); R2 representa un átomo de H o un átomo de F; R3 representa un átomo de F; y sales, isómeros, tautómeros, solvatos e hidratos de los mismos. Estos compuestos son inhibidores efectivos, estables y seguros de la enzima dipeptidil-peptidasa-IV (DPP-IV), y son adecuados para el tratamiento y la prevención de la diabetes y de otras enfermedades relacionadas con la actividad enzimática de la DPP-IV: También describe el uso de estos compuestos para la preparación de una formulación farmacéutica, una formulación farmacéutica que comprende un compuesto de fórmula (1), y un procedimiento para la preparación de los compuestos de fórmula (1). Asimismo, se describen los intermediarios que se utilizan en la preparación de dichos compuestos de fórmula (1).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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HU0200849A HUP0200849A2 (hu) | 2002-03-06 | 2002-03-06 | N-aminoacetil-2-ciano-pirrolidin-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra |
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ARP030100723A AR038868A1 (es) | 2002-03-06 | 2003-03-05 | Derivados de 1-(2-aminoacetil)2-pirrolidincarbonitrilo, su uso para la preparacion de una formulacion farmaceutica, las formulaciones farmaceuticas que los contienen, un procedimiento para la preparacion de estos derivados, y los intermediarios y su uso en dicho procedimiento de preparacion |
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US (3) | US7348327B2 (es) |
EP (1) | EP1487807B1 (es) |
JP (1) | JP4559737B2 (es) |
KR (1) | KR100977898B1 (es) |
CN (2) | CN1639159A (es) |
AR (1) | AR038868A1 (es) |
AT (1) | ATE443054T1 (es) |
AU (1) | AU2003209514B2 (es) |
BR (1) | BR0307960A (es) |
CA (1) | CA2475312C (es) |
DE (1) | DE60329282D1 (es) |
EA (1) | EA007410B1 (es) |
EC (1) | ECSP045274A (es) |
HR (1) | HRP20040910A2 (es) |
HU (1) | HUP0200849A2 (es) |
IL (2) | IL163286A (es) |
IS (1) | IS7434A (es) |
MA (1) | MA27105A1 (es) |
MX (1) | MXPA04008613A (es) |
NO (1) | NO20044221L (es) |
NZ (1) | NZ535662A (es) |
PL (1) | PL371099A1 (es) |
RS (1) | RS79004A (es) |
TN (1) | TNSN04141A1 (es) |
TW (1) | TWI250978B (es) |
UA (1) | UA78291C2 (es) |
WO (1) | WO2003074500A2 (es) |
ZA (1) | ZA200406467B (es) |
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