AR077140A1 - Derivados de pirazina como inhibidores de dgat-1, un proceso para prepararlos y una composicion farmaceutica que los comprende - Google Patents
Derivados de pirazina como inhibidores de dgat-1, un proceso para prepararlos y una composicion farmaceutica que los comprendeInfo
- Publication number
- AR077140A1 AR077140A1 ARP100102161A ARP100102161A AR077140A1 AR 077140 A1 AR077140 A1 AR 077140A1 AR P100102161 A ARP100102161 A AR P100102161A AR P100102161 A ARP100102161 A AR P100102161A AR 077140 A1 AR077140 A1 AR 077140A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- group
- cyano
- independently
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
-
- 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
- A61P3/08—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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
Abstract
Se describen compuestos inhibidores de DGAT-1 de la formula (1), sales farmacéuticamente aceptables de los mismos, junto con composiciones farmacéuticas, procesos para prepararlos y sus usos en tratar, por ejemplo la obesidad Reivindicacion 1: Un compuesto de la formula (1), o una sal farmacéuticamente aceptable del mismo, donde cada r es de manera independiente 0 o 1 y cada X1 se selecciona de manera independiente de alquilo (C1-3) lineal, alquenilo (C2-3), alquinilo (C2-3), alcoxi (C1-2), metoximetilo, amino y ciano; cada q es de manera independiente 0 o 1 y cada X2 se selecciona de manera independiente de fluor, cloro, bromo, amino, ciano, alquilo (C1-3), alquenilo (C2-3), alquinilo (C2-3) y alcoxi (C1-2); Y1 se selecciona de fluor, cloro, bromo, ciano, alquilo (C1-3) y alcoxi (C1-2); n es 0, 1 o 2 y cada Y2 se selecciona de manera independiente de fluor, cloro, bromo, ciano, hidroxi, alquilo (C1-3) y alcoxi (C1-2); p es 0, 1 o 2 y cada Y3 es de manera independiente alquilo (C1-3) o cuando p es 2 cada Y3 también se puede ligar para formar un anillo cicloalquilo (C3-5); Z es carboxi o un grupo Q seleccionado de -CONHSO2Me o uno de los anillos del grupo (2), o Z es -CONRbRc donde Rb y Rc se seleccionan de manera independiente de hidrogeno, alquilo (C1-4) y alcoxietilo (C1-4)o Rb y Rc se ligan de manera de formar un anillo morfolino o un anillo heterocíclico (C4-6), y cuando Z es -CONRbRc el grupo alquilo (C1-4) y anillos morfolino o heterocíclico (C4-6) que se pueden formar pueden estar opcionalmente sustituidos en un átomo de carbono disponible con carboxi o un grupo Q; y donde cualquier átomo de carbono en un grupo que contiene alquilo (C1-3) lineal, alquilo (C1-3) o alcoxi (C1-2) que se definio con anterioridad puede estar opcionalmente sustituido con hasta 3 átomos de fluor.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21853909P | 2009-06-19 | 2009-06-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR077140A1 true AR077140A1 (es) | 2011-08-03 |
Family
ID=42357808
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP100102161A AR077140A1 (es) | 2009-06-19 | 2010-06-18 | Derivados de pirazina como inhibidores de dgat-1, un proceso para prepararlos y una composicion farmaceutica que los comprende |
Country Status (14)
Country | Link |
---|---|
US (2) | US8188092B2 (es) |
EP (1) | EP2443096A1 (es) |
JP (1) | JP2012530122A (es) |
KR (1) | KR20120037939A (es) |
CN (1) | CN102498103A (es) |
AR (1) | AR077140A1 (es) |
AU (1) | AU2010261499A1 (es) |
BR (1) | BRPI1016109A2 (es) |
CA (1) | CA2764013A1 (es) |
MX (1) | MX2011014018A (es) |
RU (1) | RU2011152517A (es) |
TW (1) | TW201103895A (es) |
UY (1) | UY32716A (es) |
WO (1) | WO2010146395A1 (es) |
Families Citing this family (8)
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ES2359653T3 (es) * | 2006-06-08 | 2011-05-25 | Astrazeneca Ab | Bencimidazoles y su uso para el tratamiento de la diabetes. |
WO2011121350A1 (en) | 2010-04-01 | 2011-10-06 | Astrazeneca Ab | 4 -amino -7,8- dihydropyrimido [5, 4 - f] [1, 4] oxazepin- 5 ( 6h) - one based dgat1 inhibitors |
EP2684879A1 (en) | 2012-07-09 | 2014-01-15 | Basf Se | Substituted mesoionic compounds for combating animal pests |
WO2014054053A1 (en) | 2012-10-03 | 2014-04-10 | Advinus Therapeutics Limited | Spirocyclic compounds, compositions and medicinal applications thereof |
EP3495359A1 (en) * | 2013-02-04 | 2019-06-12 | Janssen Pharmaceutica NV | Flap modulators |
TWI644899B (zh) | 2013-02-04 | 2018-12-21 | 健生藥品公司 | Flap調節劑 |
CN103467392B (zh) * | 2013-10-09 | 2016-08-17 | 重庆工商大学 | 一种多卤代吡嗪甲酰胺衍生物及其盐类、制备方法和用途 |
CN103880757B (zh) * | 2014-04-15 | 2016-02-24 | 上海毕得医药科技有限公司 | 一种5-羟基嘧啶-2-羧酸的合成方法 |
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2010
- 2010-06-17 KR KR1020127001363A patent/KR20120037939A/ko not_active Application Discontinuation
- 2010-06-17 BR BRPI1016109A patent/BRPI1016109A2/pt not_active Application Discontinuation
- 2010-06-17 RU RU2011152517/04A patent/RU2011152517A/ru unknown
- 2010-06-17 CN CN201080036012XA patent/CN102498103A/zh active Pending
- 2010-06-17 WO PCT/GB2010/051003 patent/WO2010146395A1/en active Application Filing
- 2010-06-17 CA CA2764013A patent/CA2764013A1/en not_active Abandoned
- 2010-06-17 AU AU2010261499A patent/AU2010261499A1/en not_active Abandoned
- 2010-06-17 EP EP10725494A patent/EP2443096A1/en not_active Withdrawn
- 2010-06-17 JP JP2012515565A patent/JP2012530122A/ja active Pending
- 2010-06-17 TW TW099119725A patent/TW201103895A/zh unknown
- 2010-06-17 UY UY0001032716A patent/UY32716A/es unknown
- 2010-06-17 MX MX2011014018A patent/MX2011014018A/es not_active Application Discontinuation
- 2010-06-18 US US12/818,187 patent/US8188092B2/en not_active Expired - Fee Related
- 2010-06-18 AR ARP100102161A patent/AR077140A1/es unknown
-
2012
- 2012-04-25 US US13/455,275 patent/US20120289520A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
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US20120289520A1 (en) | 2012-11-15 |
JP2012530122A (ja) | 2012-11-29 |
US20100324068A1 (en) | 2010-12-23 |
AU2010261499A1 (en) | 2012-01-12 |
RU2011152517A (ru) | 2013-07-27 |
CN102498103A (zh) | 2012-06-13 |
MX2011014018A (es) | 2012-02-22 |
CA2764013A1 (en) | 2010-12-23 |
BRPI1016109A2 (pt) | 2016-05-17 |
WO2010146395A1 (en) | 2010-12-23 |
EP2443096A1 (en) | 2012-04-25 |
US8188092B2 (en) | 2012-05-29 |
KR20120037939A (ko) | 2012-04-20 |
UY32716A (es) | 2011-01-31 |
TW201103895A (en) | 2011-02-01 |
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