Recherche de Sous-structure

O=Cc1ccncc1

CC(C)(C)OC(=O)Nc1cc(C(=O)O)cc(Cl)n1
Reaction #244
Rendement 0.0%
COC(=O)c1ccnc(N(C)c2ccc(F)cc2)c1
Reaction #680
Rendement 0.0%
COC(=O)c1ccnc(N(C)c2ccc(F)cc2)c1
Reaction #681
Rendement 0.0%
CCOC(=O)c1cc(-c2ccc(OC)cc2)[nH]c(=O)c1C(=O)OCC
Reaction #65759
3,4-Diethoxycarbonyl-6-(4-methoxyphenyl)-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccc(OCOCCOC)cc2)[nH]c(=O)c1C(=O)OCC
Reaction #65765
3,4-Diethoxycarbonyl-6-(4-methoxyethoxymethoxyphenyl)-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1Nc1ccc(SC(F)(F)F)cc1
Reaction #67879
desired product
Rendement 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72040
title compound
Rendement 7.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)nc(N2CC[C@H](N)[C@H](OC)C2)c1
Reaction #72041
title compound
Rendement 91.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cc(C(=O)OC)cc(C)n3)C[C@H]2OC)nc1Cl
Reaction #72042
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(N2CC[C@H](N)[C@H](OC)C2)ncc1C
Reaction #72070
title compound
Rendement 18.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(CNc2cc(C(=O)O)ccn2)c2ccccc21
Reaction #91361
title compound
Rendement 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)nc(NS(C)(=O)=O)c1
Reaction #161765
methyl 2-chloro-6-methanesulphonylamino-isonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cc(C(=O)O)cc(Cl)n1
Reaction #161766
2-chloro-6-methanesulphonylamino-isonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)c1)N1CCc2cc(F)ccc21
Reaction #161803
1-[4′-(5-fluoro-2,3-dihydroindole-1-carbonyl)-3,4,5,6-tetrahydro-2H-[1.2′]bipyridinyl-4-yl]-1,3-dihydroimidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)c1)N1CCc2c1ccc(F)c2F
Reaction #161846
1-[4′-(4,5-difluoro-2,3-dihydro-indole-1-carbonyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)c1)N1CCc2cc(F)c(F)cc21
Reaction #161847
1-[4′-(5,6-difluoro-2,3-dihydro-indole-1-carbonyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CC(C)(C)c3cc(F)ccc32)cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)n1
Reaction #161853
1-[4′-(5-fluoro-3,3-dimethyl-2,3-dihydro-indole-1-carbonyl)-6′-methoxy-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N2CCc3c2ccc(F)c3F)cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)n1
Reaction #161856
1-[4′-(4,5-difluoro-2,3-dihydro-indole-1-carbonyl)-6′-methoxy-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)nc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)c1)N1CCc2cc(F)ccc21
Reaction #161869
1-[6′-chloro-4′-(5-fluoro-2,3-dihydro-indole-1-carbonyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(N2CCN3CCC2CC3)ncc1N
Reaction #164578
5-amino-2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-N-methylisonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
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