ECSP003687A - DERIVATIVES 1 OF QUINOLIN-4- IL - Google Patents
DERIVATIVES 1 OF QUINOLIN-4- ILInfo
- Publication number
- ECSP003687A ECSP003687A ECSP003687A ECSP003687A EC SP003687 A ECSP003687 A EC SP003687A EC SP003687 A ECSP003687 A EC SP003687A EC SP003687 A ECSP003687 A EC SP003687A
- Authority
- EC
- Ecuador
- Prior art keywords
- lower alkyl
- phenyl
- amino
- hydrogen
- quinolinyl
- Prior art date
Links
- -1 chroman-6-yl Chemical group 0.000 abstract 13
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000003282 alkyl amino group Chemical group 0.000 abstract 4
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000005037 alkyl phenyl group Chemical group 0.000 abstract 1
- 125000004244 benzofuran-2-yl group Chemical group [H]C1=C(*)OC2=C([H])C([H])=C([H])C([H])=C12 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
El invento se refiere a compuestos de la fórmula: (gráfico), en donde R1 es hidrógeno, alquilo inferior, alcoxilo inferior, hidroxilo, amino, nitro, ciano, alquilo inferior-amino, di-alquil-amino inferior o halógeno; R2 es fenilo, opcionalmente sustituido por alquilo inferior, alcoxilo inferior, halógeno, trifluorometilo, amino, alquil-amino inferior o di-alquil-amino inferior, 2,3-dihidro-benzofuran-5-ilo, croman-6-ilo, naftalen-2-ilo, indan-5-ilo, alquilen-fenilo inferior, 5,6,7,8-tetrahidro-naftalenilo, 2,3-dihidro-isoindol-2-ilo, 1,2,3,4-tetrahidro -naftalenilo, benzofuran-2-ilo, benzo[b] tiofen-2-ilo, alquil-fenilo inferior, 3,4-di-hidro-1H-isoquinolin-2-ilo o tiofen-3-ilo; R3 y R4 son independientemente uno de otro hidrógeno o alquilo inferior; R3 es hidrógeno, alquilo inferior, -CH2OH o -CH2NR6R7; R6 y R7 son independientemente uno de otro, hidrógeno, alquilo inferior, -(CH2)n-fenilo, cicloalquilo, -(CH2)m-morfolinilo o forman junto con el átomo de N un anillo saturado con4-6 átomos de C; n es 0-3; m es 2-3,. m es 2-3; X es -NR8-u -O-; o X y R5 son, conjuntamente, >N(CH2)2-; o X y R3 son, conjuntamente, >N(CH2)3-; y R8 es hidrógeno o alquilo inferior; y sus sales de adición de ácido farmacéuticamente aceptables, con la excepción de los compuestos siguientes (6-cloro-2-fenil-4-quinolinil)-(+)-2-aminobutano1; (6-metil-2-fenil-4-quinolinil)-(+)-2-aminobutano1; (6-metoxi-2-fenil-4-quinolinil)-(+)-2-aminobutano1; y (8-metoxi-2-fenil-4-quinolinil)-(+)-2-aminobutano1;The invention relates to compounds of the formula: (graph), wherein R 1 is hydrogen, lower alkyl, lower alkoxy, hydroxyl, amino, nitro, cyano, lower alkyl-amino, di-lower alkyl amino or halogen; R2 is phenyl, optionally substituted by lower alkyl, lower alkoxy, halogen, trifluoromethyl, amino, lower alkyl amino or di-lower alkyl amino, 2,3-dihydro-benzofuran-5-yl, chroman-6-yl, naphthalen -2-yl, indan-5-yl, lower alkylene-phenyl, 5,6,7,8-tetrahydro-naphthalenyl, 2,3-dihydro-isoindole-2-yl, 1,2,3,4-tetrahydro - naphthalenyl, benzofuran-2-yl, benzo [b] thiophene-2-yl, lower alkyl-phenyl, 3,4-di-hydro-1H-isoquinolin-2-yl or thiophene-3-yl; R3 and R4 are independently of each other hydrogen or lower alkyl; R3 is hydrogen, lower alkyl, -CH2OH or -CH2NR6R7; R6 and R7 are independently of each other, hydrogen, lower alkyl, - (CH2) n-phenyl, cycloalkyl, - (CH2) m-morpholinyl or together with the N atom form a saturated ring with 4-6 C atoms; n is 0-3; m is 2-3 ,. m is 2-3; X is -NR8-u -O-; or X and R5 are, together,> N (CH2) 2-; or X and R3 are, together,> N (CH2) 3-; and R8 is hydrogen or lower alkyl; and its pharmaceutically acceptable acid addition salts, with the exception of the following compounds (6-chloro-2-phenyl-4-quinolinyl) - (+) - 2-aminobutane1; (6-methyl-2-phenyl-4-quinolinyl) - (+) - 2-aminobutane1; (6-methoxy-2-phenyl-4-quinolinyl) - (+) - 2-aminobutane1; and (8-methoxy-2-phenyl-4-quinolinyl) - (+) - 2-aminobutane1;
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP003687 ECSP003687A (en) | 2000-09-29 | 2000-09-29 | DERIVATIVES 1 OF QUINOLIN-4- IL |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP003687 ECSP003687A (en) | 2000-09-29 | 2000-09-29 | DERIVATIVES 1 OF QUINOLIN-4- IL |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP003687A true ECSP003687A (en) | 2001-05-23 |
Family
ID=42041277
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSP003687 ECSP003687A (en) | 2000-09-29 | 2000-09-29 | DERIVATIVES 1 OF QUINOLIN-4- IL |
Country Status (1)
| Country | Link |
|---|---|
| EC (1) | ECSP003687A (en) |
-
2000
- 2000-09-29 EC ECSP003687 patent/ECSP003687A/en unknown
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