AR027336A1 - Carboxamidas de pirimidina utiles como inhibidores de isozimas pde4. - Google Patents
Carboxamidas de pirimidina utiles como inhibidores de isozimas pde4.Info
- Publication number
- AR027336A1 AR027336A1 ARP010100435A ARP010100435A AR027336A1 AR 027336 A1 AR027336 A1 AR 027336A1 AR P010100435 A ARP010100435 A AR P010100435A AR P010100435 A ARP010100435 A AR P010100435A AR 027336 A1 AR027336 A1 AR 027336A1
- Authority
- AR
- Argentina
- Prior art keywords
- bicyclo
- octanyl
- benzopyranyl
- monocyclic
- cycloalkyl
- Prior art date
Links
- 101100296720 Dictyostelium discoideum Pde4 gene Proteins 0.000 title 1
- 101100082610 Plasmodium falciparum (isolate 3D7) PDEdelta gene Proteins 0.000 title 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- -1 2 , 3-dihydrobenzofuranyl Chemical group 0.000 abstract 25
- 125000002950 monocyclic group Chemical group 0.000 abstract 3
- UWYZHKAOTLEWKK-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2CNCCC2=C1 UWYZHKAOTLEWKK-UHFFFAOYSA-N 0.000 abstract 2
- LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000002883 imidazolyl group Chemical group 0.000 abstract 2
- 125000001544 thienyl group Chemical group 0.000 abstract 2
- 125000005871 1,3-benzodioxolyl group Chemical group 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 abstract 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000003384 isochromanyl group Chemical group C1(OCCC2=CC=CC=C12)* 0.000 abstract 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 125000005593 norbornanyl group Chemical group 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
Classifications
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- Psychiatry (AREA)
Abstract
Se describen compuestos de la formula 1. En la que j es 0 o 1; k es 0 o 1; m es 0 o 1; n es 0 o 1; W es -O-; -S(=O)t-, en el que t es 0, 1 o 2; o -N(R3)-;en el que R3 es -H; -alquilo (C1-3); -OR12; fenilo, o bencilo; RC y RD tienen el mismo significa do que RA y RB salvo porque al menos uno de RC y RD debe ser-H, ZA es (a) un grupo heterocíclico (C3-9) saturado o insaturado, fusionado o abierto, cíclico o bicíclico seleccionado entre furanilo, tienilo, pirrolilo,pirrolidinilo, oxazolilo, isoxazol ilo, tiazolilo, isotiazolilo, morfolinilo, pirazolilo, oxadiazolilo, tiadiazolilo, imidazolilo, pirazinilo, pirimidinilo,piridazinilo, piperidinilo, piperazinilo, triazolilo, tetrazolilo, 2,3-benzofuranilo, 2,3-dihidrobenzofuranilo, 1,3-dihidroisoben zofuranilo, benzo[b]tienilo,indolilo, indolinilo, isoindolinilo, 2-H-1-benzopiranilo, 4H-1-benzopiranilo, 1H-2-benzopiranilo, cromanilo, isocromanilo, quinoleilo, isoquinoleilo, 1,2,3,4-tetrahidroquinoleilo, 1,2,3,4-tetrahidroisoquinoleilo, quinuclid inilo, azabiciclo[3.3.0]octanilo, 1,3-benzodioxolilo, 3H-2,1-benzoxatiolilo, benzoxazolilo,1,2-benzoisoxazolilo, 2,1-benzoisoxazolilo, 1,2-benzoditiolilo, 1,3-benzoditiolilo, benzotiazolilo, 1,2-benzoisotiazolilo, benzoimidazolilo, imidazolilo,1,4-be nzodioxanilo, 4H-3,1-benzoxazinilo, 2H-1,4-benzoxazinilo, 1,4-benzotiazinilo, 1,2-benzotiazinilo quinazolinilo, quinoxalinilo, ftalazinilo, cinnolinilo,1,2,3-benzotiadiazolilo, 2H-1,2,4-benzotiadiazinilo, 2H-1,2,4-benzoxadiazinilo, benzoxatriazinilo, 1,2,3-benzotriazinilo, 1,2,4-benzotriazinilo ybenzotetrazinilo; o Z es (b) un resto cicloalquilo (C3-7) monocíclico; un resto cicloalquenilo (C5-7) monocíclico que es un miembro seleccionado del grupo queconsiste en ciclopentenilo, ciclohexenilo y c icloheptenilo; o un resto cicloalquilo (C7-10) o cicloalquenilo (C7-10) bicíclico que es un miembro seleccionadodel grupo que consiste en norbornanilo, norbonenilo, biciclo[2.2.2]octanilo, biciclo[3.2.1.]ocatanilo, biciclo[3.3.0]octanilo, biciclo[2.2 .2]oct-5-enilo,biciclo-[2.2.2]oct-7-enilo, biciclo[3.3.1]nonanilo, ciclodecanilo y adamantanilo; en el que dichos restos cicloalquilo monocíclicos y bicíclicos están
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|---|---|---|---|
| US17928200P | 2000-01-31 | 2000-01-31 |
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| ARP010100435A AR027336A1 (es) | 2000-01-31 | 2001-01-31 | Carboxamidas de pirimidina utiles como inhibidores de isozimas pde4. |
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