AR039041A1 - Derivados de ciclopenteno - Google Patents
Derivados de ciclopentenoInfo
- Publication number
- AR039041A1 AR039041A1 ARP030100983A ARP030100983A AR039041A1 AR 039041 A1 AR039041 A1 AR 039041A1 AR P030100983 A ARP030100983 A AR P030100983A AR P030100983 A ARP030100983 A AR P030100983A AR 039041 A1 AR039041 A1 AR 039041A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- hydrogen
- amino
- group
- Prior art date
Links
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical class C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- -1 cyano, hydroxy Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 208000001435 Thromboembolism Diseases 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000002433 cyclopentenyl group Chemical class C1(=CCCC1)* 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
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- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/04—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D309/06—Radicals substituted by oxygen atoms
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- A—HUMAN NECESSITIES
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- C07C205/08—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to acyclic carbon atoms
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- C07C251/44—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atom of at least one of the oxyimino groups being part of a ring other than a six-membered aromatic ring
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La presente se refiere a derivados de ciclopenteno sustituidos, a un procedimiento para su preparación, así como a su uso para la preparación de medicamentos, especialmente para el tratamiento y/o la prevención de enfermedades tromboembólicas. Reivindicación 1: Compuestos de fórmula (1) en la que: R1 designa arilo (C6-10) o heteroarilo de 5 ó 6 miembros con hasta dos heteroátomos del grupo de N, O y/o S, que pueden estar sustituidos respectivamente de una a tres veces independientemente entre sí con restos seleccionados del grupo de halógeno, alquilo (C1-6), trifluorometilo, ciano, hidroxi, alcoxi (C1-6), trifluorometoxi, carboxilo, alcoxi(C1-4)-carbonilo, -C(O)-NR9R10, amino, mono- y dialquil(C1-6)-amino, en los que los restos alquilo y alcoxi anteriormente citados pueden estar sustituidos respectivamente a su vez con hidroxi, alcoxi (C1-4), carboxilo, alcoxi(C1-4)-carbonilo, amino, mono-, o dialquil(C1-4)-amino; y R9 y R10 significan independientemente entre sí hidrógeno o alquilo (C1-6); A designa un enlace o alcano(C1-4)-diilo, alqueno(C2-4)-diilo o alquino(C2-4)-diilo; R2 y R5 designan independientemente entre sí piridilo, tienilo, furilo, benzofuranilo, tetrahidropiranilo, ciclohexilo, o fenilo, que pueden estar sustituidos respectivamente una o dos veces independientemente entre sí con halógeno, alquilo (C1-6), trifluorometilo, ciano, amino, alcoxi (C1-6) o trifluorometoxi, en los que los restos alquilo y alcoxi anteriormente citados pueden estar sustituidos a su vez respectivamente con hidroxi, alcoxi (C1-4), carboxilo, alcoxi(C1-4)-carbonilo, amino, mono- o dialquil(C1-4)-amino; R3 y R4 designan independientemente entre sí hidrógeno, alquilo (C1-6), alquenilo (C2-6) ,alquinilo (C2-6) o cicloalquilo (C3-8), que pueden estar sustituidos respectivamente de una a tres veces independientemente entre sí con restos seleccionados del grupo de hidroxi, alcoxi (C1-6), ciano, flúor, cloro, -NR11R12, -C(O)-OR13, -C(O)-NR11R12, -SO2-OR13 y -SO2-OR3, en los que R11, R12 y R13 significan independientemente entre sí hidrógeno o alquilo (C1-6), o R3 y R4 junto con el átomo de carbono al que están unidos forman un anillo cicloalquilo con enlace espiro de 3 a 6 miembros; R6 designa hidrógeno, alquilo (C1-6), alcanoilo (C1-6) o un grupo de fórmula -C(O)-C(O)-OR14, en la que R14 significa hidrógeno o alquilo (C1-6); R7 designa hidrógeno; R8 designa hidroxi; o R7 y R8 junto con el átomo de carbono al que están unidos forman un grupo carbonilo o un grupo de fórmula C=N-O-R15, en la que R15 designa hidrógeno o alquilo (C1-6), que puede estar sustituido con hidroxi, alcoxi (C1-6), carboxilo, alcoxi(C1-4)-carbonilo o un grupo de fórmula -NR16R17 o -C(O)-NR16R17, en al que R16 y R17 significan independientemente entre sí hidrógeno o alquilo (C1-6); y sus sales, solvatos y solvatos de las sales para combatir enfermedades.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10213228A DE10213228A1 (de) | 2002-03-25 | 2002-03-25 | Cyclopenten-Derivate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR039041A1 true AR039041A1 (es) | 2005-02-02 |
Family
ID=28050808
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030100983A AR039041A1 (es) | 2002-03-25 | 2003-03-20 | Derivados de ciclopenteno |
Country Status (9)
| Country | Link |
|---|---|
| AR (1) | AR039041A1 (es) |
| AU (1) | AU2003209728A1 (es) |
| DE (1) | DE10213228A1 (es) |
| GT (1) | GT200300066A (es) |
| HN (1) | HN2003000104A (es) |
| PE (1) | PE20040163A1 (es) |
| TW (1) | TW200400936A (es) |
| UY (1) | UY27733A1 (es) |
| WO (1) | WO2003080553A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7550499B2 (en) | 2004-05-12 | 2009-06-23 | Bristol-Myers Squibb Company | Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| JP2008527043A (ja) * | 2005-01-19 | 2008-07-24 | ブリストル−マイヤーズ スクイブ カンパニー | 血栓塞栓障害治療用のp2y1受容体阻害剤としての2−フェノキシ−n−(1,3,4−チアジアゾール−2−イル)ピリジン−3−アミン誘導体および関連化合物 |
| US7714002B2 (en) | 2005-06-27 | 2010-05-11 | Bristol-Myers Squibb Company | Carbocycle and heterocycle antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| WO2007002584A1 (en) | 2005-06-27 | 2007-01-04 | Bristol-Myers Squibb Company | Linear urea mimics antagonists of p2y1 receptor useful in the treatment of thrombotic conditions |
| WO2007002635A2 (en) | 2005-06-27 | 2007-01-04 | Bristol-Myers Squibb Company | C-linked cyclic antagonists of p2y1 receptor useful in the treatment of thrombotic conditions |
| US7728008B2 (en) | 2005-06-27 | 2010-06-01 | Bristol-Myers Squibb Company | N-linked heterocyclic antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| TWI499414B (zh) | 2006-09-29 | 2015-09-11 | Lexicon Pharmaceuticals Inc | 鈉與葡萄糖第2型共同運輸體(co-transporter 2)的抑制物與其應用方法 |
| US7960569B2 (en) | 2006-10-17 | 2011-06-14 | Bristol-Myers Squibb Company | Indole antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
| WO2008109591A1 (en) | 2007-03-08 | 2008-09-12 | Lexicon Pharmaceuticals, Inc. | Phlorizin analogs as inhibitors of sodium glucose co-transporter 2 |
| US11884640B2 (en) * | 2021-06-02 | 2024-01-30 | Chirogate International Inc. | Processes and intermediates for the preparations of benzoprostacyclin analogues and benzoprostacyclin analogues prepared therefrom |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3888905A (en) * | 1969-02-17 | 1975-06-10 | Searle & Co | Prostaglandin intermediates and optically active isomers thereof |
| GB1461789A (en) * | 1973-04-12 | 1977-01-19 | Lilly Industries Ltd | 3-substituted propanoic acid derivatives |
-
2002
- 2002-03-25 DE DE10213228A patent/DE10213228A1/de not_active Withdrawn
-
2003
- 2003-03-12 WO PCT/EP2003/002532 patent/WO2003080553A1/de not_active Ceased
- 2003-03-12 AU AU2003209728A patent/AU2003209728A1/en not_active Abandoned
- 2003-03-20 AR ARP030100983A patent/AR039041A1/es not_active Application Discontinuation
- 2003-03-24 GT GT200300066A patent/GT200300066A/es unknown
- 2003-03-24 HN HN2003000104A patent/HN2003000104A/es unknown
- 2003-03-24 PE PE2003000288A patent/PE20040163A1/es not_active Application Discontinuation
- 2003-03-24 TW TW092106432A patent/TW200400936A/zh unknown
- 2003-03-25 UY UY27733A patent/UY27733A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| HN2003000104A (es) | 2003-12-15 |
| PE20040163A1 (es) | 2004-04-22 |
| GT200300066A (es) | 2004-02-12 |
| WO2003080553A1 (de) | 2003-10-02 |
| TW200400936A (en) | 2004-01-16 |
| DE10213228A1 (de) | 2003-10-16 |
| AU2003209728A1 (en) | 2003-10-08 |
| UY27733A1 (es) | 2003-10-31 |
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| Date | Code | Title | Description |
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| FA | Abandonment or withdrawal |