BRPI0513359A - tetraidroisoquinolinas substituìdas por arila e heteroarila e uso destes para bloquear a recaptação de norepinefrina, dopamina, e serotonina - Google Patents
tetraidroisoquinolinas substituìdas por arila e heteroarila e uso destes para bloquear a recaptação de norepinefrina, dopamina, e serotoninaInfo
- Publication number
- BRPI0513359A BRPI0513359A BRPI0513359-9A BRPI0513359A BRPI0513359A BR PI0513359 A BRPI0513359 A BR PI0513359A BR PI0513359 A BRPI0513359 A BR PI0513359A BR PI0513359 A BRPI0513359 A BR PI0513359A
- Authority
- BR
- Brazil
- Prior art keywords
- pyridinyl
- quinolinyl
- quinazinyl
- benzo
- serotonin
- Prior art date
Links
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 title abstract 4
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 title abstract 2
- 229960002748 norepinephrine Drugs 0.000 title abstract 2
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 title abstract 2
- 229940076279 serotonin Drugs 0.000 title abstract 2
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 title 2
- 125000003118 aryl group Chemical group 0.000 title 1
- 229960003638 dopamine Drugs 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 title 1
- 150000003526 tetrahydroisoquinolines Chemical class 0.000 title 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 5
- -1 benzoisothiazolyl Chemical group 0.000 abstract 4
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 4
- 125000005605 benzo group Chemical group 0.000 abstract 3
- 125000002619 bicyclic group Chemical group 0.000 abstract 2
- 125000004529 1,2,3-triazinyl group Chemical group N1=NN=C(C=C1)* 0.000 abstract 1
- 125000004530 1,2,4-triazinyl group Chemical group N1=NC(=NC=C1)* 0.000 abstract 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 abstract 1
- 125000000850 2H-chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 abstract 1
- VYFYYTLLBUKUHU-WTJCDBBSSA-N 4-(2-amino-1,1-ditritioethyl)benzene-1,2-diol Chemical compound NCC([3H])([3H])C1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-WTJCDBBSSA-N 0.000 abstract 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000001819 4H-chromenyl group Chemical group O1C(=CCC2=CC=CC=C12)* 0.000 abstract 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 1
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000005872 benzooxazolyl group Chemical group 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000002618 bicyclic heterocycle 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
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000723 dihydrobenzofuranyl group Chemical group O1C(CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000005436 dihydrobenzothiophenyl group Chemical group S1C(CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
Classifications
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- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4741—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having oxygen as a ring hetero atom, e.g. tubocuraran derivatives, noscapine, bicuculline
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- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
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- C07D217/08—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with a hetero atom directly attached to the ring nitrogen atom
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Abstract
TETRAIDROISOQUINOLINAS SUBSTITUìDAS POR ARILA E HETEROARILA E USO DESTES PARA BLOQUEAR A RECAPTAçãO DE NOREPINEFRINA, DOPAMINA, E SEROTONINA. A presente invenção refere-se aos compostos da presente invenção que são representados pela estrutura química encontrada na Fórmula (I): em que: o átomo de carbono designado * está na configuração R ou S; e X é um carbociclo bicíclico fundido ou heterociclo selecionado do grupo que consiste em benzofuranila, benzo¢b!tiofenila, benzoisotiazolila, benzoisoxazolila, indazolila, indolila, isoindolila, indolizinila, benzoimidazolila, benzooxazolila, benzotiazolila, benzotriazolila, imidazo¢1 ,2-a! piridinila, pirazol¢1 .5-a! piridinila, ¢1 ,2,4!triazol¢4,3-a!piridinila, tieno¢2,3-b! piridinila, tieno ¢3,2-b! piridinila, 1 H-pirrol¢2,3-b!piridinila, indenila, indanila, diidrobenzocicloeptenila, tetraidrobenzocicloeptenila, diidrobenzotiofenila, diidrobenzofuranila, indolinila, naftila, tetraidronaifila, quinolinila, isoquinolinila, 4H-quinolizinila, 9aH-quinolizinila, quinazolinila, cinolinila, ftalazinila, quinoxalinila, benzo ¢1 ,2,3!triazinila, benzo¢1 ,2,4!triazinila, 2H- cromenila, 4H-cromenila, e um carbociclo bicíclico fundido ou heterociclo bicíclico fundido opcionalmente substituído por substituintes (número 1 a 4) como definido em R¬ 14¬com R¬ 1¬, R¬ 2¬, R¬ 3¬, R¬ 4¬, R¬ 5¬, R¬ 6¬ R¬ 7¬, R¬ 8¬, e R¬ 14¬ definidos aqui.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58844804P | 2004-07-15 | 2004-07-15 | |
| PCT/US2005/025193 WO2006020049A2 (en) | 2004-07-15 | 2005-07-15 | Aryl-and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
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| Publication Number | Publication Date |
|---|---|
| BRPI0513359A true BRPI0513359A (pt) | 2008-05-06 |
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| Application Number | Title | Priority Date | Filing Date |
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| BRPI0513359-9A BRPI0513359A (pt) | 2004-07-15 | 2005-07-15 | tetraidroisoquinolinas substituìdas por arila e heteroarila e uso destes para bloquear a recaptação de norepinefrina, dopamina, e serotonina |
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| EP (1) | EP1778639B1 (pt) |
| JP (2) | JP5007226B2 (pt) |
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| AU (1) | AU2005274927B2 (pt) |
| BR (1) | BRPI0513359A (pt) |
| CA (1) | CA2573271C (pt) |
| GE (1) | GEP20094640B (pt) |
| IL (1) | IL180349A (pt) |
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| UA (1) | UA91341C2 (pt) |
| WO (1) | WO2006020049A2 (pt) |
| ZA (1) | ZA200701232B (pt) |
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