CO6670576A2 - Compuestos hetericíclicos fusionados como inhibidores de fosfodiesterasas 10a - Google Patents
Compuestos hetericíclicos fusionados como inhibidores de fosfodiesterasas 10aInfo
- Publication number
- CO6670576A2 CO6670576A2 CO13011489A CO13011489A CO6670576A2 CO 6670576 A2 CO6670576 A2 CO 6670576A2 CO 13011489 A CO13011489 A CO 13011489A CO 13011489 A CO13011489 A CO 13011489A CO 6670576 A2 CO6670576 A2 CO 6670576A2
- Authority
- CO
- Colombia
- Prior art keywords
- ring
- optionally substituted
- group
- formula
- membered
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 101001072037 Homo sapiens cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A Proteins 0.000 title 1
- 102100036377 cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A Human genes 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
Classifications
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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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/4355—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
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- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La presente invención proporciona un compuesto que tiene el efecto de la inhibición de PDE y que es de utilidad como un agente para prevenir o tratar esquizofrenia, etc.Un compuesto representado por la fórmula (I):en donde anillo A representa un anillo de 6 miembros opcionalmente sustituido; uno o dos cualesquiera de Za Zrepresenta -N= y los otros representan -CH;Y representa un átomo de oxígeno, un átomo de azufre, un grupo metileno opcionalmente sustituido o NR-;Rrepresenta un átomo de hidrógeno o un sustituyente; yR representaun grupo representado por la fórmula:en dondeRrepresenta un grupo fenilo o grupo heterocíclico de 5 a 10 miembros, cada uno de los cuales está opcionalmente sustituido; L representa un átomo de azufre, un átomo de oxígeno, un grupo metileno opcionalmente sustituido, -CO-, -NRa-, CHO-, -NRCOO-, -NRCONR-, -NRCOCH-, -NRCO-,R: y Rson iguales o diferentes y cada uno representa un átomo de hidrógeno o un grupo alquilo Copcionalmente sustituido, oL y Ropcionalmente forman, en combinación, un grupo heterocíclico fusionado bi- o tricíclico opcionalmente sustituido; y el anillo Brepresenta un anillo benceno, un anillo piridina, un anillo pirimidina, un anillo pirazina o un anillo piridazina, cada uno de los cuales está opcionalmente sustituido; o(2) un grupo representado por la fórmula:en dondeRrepresenta un grupo fenilo o grupo heterocíclico de 5 a 10 miembros, cada uno de los cuales está opcionalmente sustituido;el anillo Brepresenta un anillo benceno, un anillo piridina, un anillo pirimidina, un anillo pirazina o un anillo piridazina, cada uno de los cuales está opcionalmente sustituido; y el anillo D representa un anillo de 5 ó 6 miembros también opcionalmente sustituido; o una de sus sales.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35812110P | 2010-06-24 | 2010-06-24 | |
| US42284510P | 2010-12-14 | 2010-12-14 |
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| CO6670576A2 true CO6670576A2 (es) | 2013-05-15 |
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| CO13011489A CO6670576A2 (es) | 2010-06-24 | 2013-01-22 | Compuestos hetericíclicos fusionados como inhibidores de fosfodiesterasas 10a |
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| KR (1) | KR101875238B1 (es) |
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| AR (1) | AR081976A1 (es) |
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| BR (1) | BR112012032087A2 (es) |
| CA (1) | CA2803156C (es) |
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| CO (1) | CO6670576A2 (es) |
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| CN103476757A (zh) | 2011-02-18 | 2013-12-25 | 阿勒根公司 | 作为磷酸二酯酶10(pde10a)的抑制剂的取代的6,7-二烷氧基-3-异喹啉醇衍生物 |
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| WO2014071044A1 (en) | 2012-11-01 | 2014-05-08 | Allergan, Inc. | Substituted 6,7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (pde10a) |
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