PE20020065A1 - DERIVATIVES OF 2-AMINOCARBONYL-9H-PURINE - Google Patents

DERIVATIVES OF 2-AMINOCARBONYL-9H-PURINE

Info

Publication number
PE20020065A1
PE20020065A1 PE2001000520A PE2001000520A PE20020065A1 PE 20020065 A1 PE20020065 A1 PE 20020065A1 PE 2001000520 A PE2001000520 A PE 2001000520A PE 2001000520 A PE2001000520 A PE 2001000520A PE 20020065 A1 PE20020065 A1 PE 20020065A1
Authority
PE
Peru
Prior art keywords
alkyl
amino
carbonyl
purine
ilo
Prior art date
Application number
PE2001000520A
Other languages
Spanish (es)
Inventor
Peter Thomas Stephenson
Simon John Mantell
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB0024920A external-priority patent/GB0024920D0/en
Application filed by Pfizer filed Critical Pfizer
Publication of PE20020065A1 publication Critical patent/PE20020065A1/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

SE REFIERE A DERIVADOS DE 2-AMINOCARBONIL-9H-PURINA DE FORMULA I DONDE R1 ES H, ALQUILO C1-C6, FLUORENILO, SUSTITUIDO cON FENILO, NAFTILO, ENTRE OTROS; R2 ES H, ALQUILO C1-C6; R15 ES H, ALQUILO C1-C6; X ES i) ALQUILENO C2-C3 NO RAMIFICADO SUSTITUIDO CON ALQUILO C1-C6, CICLOALQUILO C3-C8, ii) UN GRUPO DE FORMULA -(CH2)n-W-(CH2)p DONDE W ES CICLOALQUILENO C5-C7 CON ALQUILO C1-C6; n Y p SON 0-1; R3 ES H, ALQUILO C1-C6, CICLOALQUILO C3-C8, BENCILO; R4 ES AZETIDIN-3-ILO, PIRROLIDIN-3-ILO,PIPERIDIN 3-ILO, ENTRE OTROS; R3 Y R4 JUNTO A N FORMAN AZETIDINILO, PIRROLIDINILO, PIPERIDINILO, PIPERAZINILO, HOMOPIPERIDINILO, ENTRE OTROS; R5 ES CH2OH, CONR14R14; R6 Y R7 SON H, ALQUILO C1-C6 O JUNTO A N FORMAN AZETIDINILO, PIRROLIDINILO, ENTRE OTROS; R14 ES H, ALQUILO C1-C6; Y ES CO, CS, SO2, C=N(CN). SON COMPUESTOS PREFERIDOS 6-[(2,2-DIFENILETIL)AMINO]-9-{(2R,3R,4S,5S)-5-[(ETILAMINO)CARBONIL]-3,4-DIHIDROXITETRAHIDRO-2-FURANIL}-N-{2-[({[1-(2-PIRIDINIL)-4-PIPERIDINIL]AMINO}CARBONIL)AMINO]-ETIL}-9H-PURINA-2-CARBOXAMIDA, 4-[({[(2-{[(6-[(2,2-DIFENILETIL)AMINO]-9-{(2R,3R,4S,5S)-5-[(ETILAMINO)CARBONIL]-3,4-DIHIDRO-2-FURANIL}-9H-PURIN-2-IL)CARBONIL]AMINO}ETIL}AMINO]-CARBONIL}-AMINO)METIL]BENZOICO. SE REFIERE TAMBIEN A UN COMPOSICION FARMACEUTICA. LOS DERIVADOS DE 2-AMINOCARBONIL-9H-PURINA SON AGONISTAS DEL RECEPTOR A2a Y ACTUAN COMO AGENTES ANTIINFLAMATORIOREFERS TO 2-AMINOCARBONYL-9H-PURINE DERIVATIVES OF FORMULA I WHERE R1 IS H, C1-C6 ALKYL, FLUORENIL, SUBSTITUTED WITH PHENYL, NAPHTHYLL, AMONG OTHERS; R2 IS H, C1-C6 ALKYL; R15 IS H, C1-C6 ALKYL; X IS i) NON-BRANCHED C2-C3 ALKYLENE SUBSTITUTED WITH C1-C6 ALKYL, C3-C8 CYCLOALKYL, ii) A GROUP OF FORMULA - (CH2) nW- (CH2) p WHERE W IS C5-C7 CYCLOALKYLENE WITH C1-C6 ALKYL ; n and p ARE 0-1; R3 IS H, C1-C6 ALKYL, C3-C8 CYCLOALkyl, BENZYL; R4 IS AZETIDIN-3-ILO, PIRROLIDIN-3-ILO, PIPERIDIN 3-ILO, AMONG OTHERS; R3 AND R4 TOGETHER WITH N FORM AZETIDINYL, PYRROLIDINYL, PIPERIDINYL, PIPERAZINYL, HOMOPIPERIDINYL, AMONG OTHERS; R5 IS CH2OH, CONR14R14; R6 AND R7 ARE H, C1-C6 ALKYL OR TOGETHER WITH N FORMING AZETHYDINYL, PYRROLIDINYL, AMONG OTHERS; R14 IS H, C1-C6 ALKYL; Y IS CO, CS, SO2, C = N (CN). PREFERRED COMPOUNDS ARE 6 - [(2,2-DIPHENYLETHYL) AMINO] -9 - {(2R, 3R, 4S, 5S) -5 - [(ETHYLAMINE) CARBONYL] -3,4-DIHYDROXITETRAHYDRO-2-FURANIL} -N - {2 - [({[1- (2-PYRIDINYL) -4-PIPERIDINYL] AMINO} CARBONYL) AMINO] -ETHYL} -9H-PURINE-2-CARBOXAMIDE, 4 - [({[(2 - {[( 6 - [(2,2-DIPHENYLETHYL) AMINO] -9 - {(2R, 3R, 4S, 5S) -5 - [(ETHYLAMINE) CARBONYL] -3,4-DIHYDRO-2-FURANIL} -9H-PURIN- 2-IL) CARBONYL] AMINO} ETHYL} AMINO] -CARBONYL} -AMINE) METHYL] BENZOIC. ALSO REFERS TO A PHARMACEUTICAL COMPOSITION. DERIVATIVES OF 2-AMINO CARBONYL-9H-PURINE ARE A2a RECEPTOR AGONISTS AND ACT AS ANTI-INFLUENCE AGENTS

PE2001000520A 2000-06-06 2001-06-05 DERIVATIVES OF 2-AMINOCARBONYL-9H-PURINE PE20020065A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0014048A GB0014048D0 (en) 2000-06-06 2000-06-06 Purine derivatives
GB0018246A GB0018246D0 (en) 2000-06-06 2000-07-25 Purine derivatives
GB0024920A GB0024920D0 (en) 2000-06-06 2000-10-11 Purine derivatives

Publications (1)

Publication Number Publication Date
PE20020065A1 true PE20020065A1 (en) 2002-02-12

Family

ID=9893285

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2001000520A PE20020065A1 (en) 2000-06-06 2001-06-05 DERIVATIVES OF 2-AMINOCARBONYL-9H-PURINE

Country Status (15)

Country Link
CN (1) CN100374454C (en)
AP (1) AP2001002179A0 (en)
CR (1) CR6829A (en)
DO (1) DOP2001000182A (en)
EC (1) ECSP024370A (en)
GB (2) GB0014048D0 (en)
GE (1) GEP20053513B (en)
GT (1) GT200100105A (en)
IL (1) IL152783A (en)
MY (1) MY128457A (en)
PE (1) PE20020065A1 (en)
SV (1) SV2002000477A (en)
TN (1) TNSN01083A1 (en)
YU (1) YU82302A (en)
ZA (1) ZA200209875B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105481861B (en) * 2014-09-19 2018-04-17 北京普禄德医药科技有限公司 A kind of platelet aggregation inhibitor and its preparation method and application

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1121372B1 (en) * 1998-10-16 2006-06-28 Pfizer Limited Adenine derivatives

Also Published As

Publication number Publication date
CN100374454C (en) 2008-03-12
DOP2001000182A (en) 2002-08-30
ECSP024370A (en) 2003-03-10
GB0014048D0 (en) 2000-08-02
IL152783A (en) 2008-11-26
CN1810822A (en) 2006-08-02
YU82302A (en) 2005-11-28
GEP20053513B (en) 2005-05-10
ZA200209875B (en) 2003-12-05
CR6829A (en) 2004-03-11
GT200100105A (en) 2002-01-31
MY128457A (en) 2007-02-28
AP2001002179A0 (en) 2002-11-30
SV2002000477A (en) 2002-10-24
GB0018246D0 (en) 2000-09-13
TNSN01083A1 (en) 2005-11-10

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Legal Events

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FD Application declared void or lapsed