Participa en 21 reacciones

678180

O=C1Nc2cc(CO)cnc2N2CCCCC12
Reaction #156800
title compound
Rendimiento 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CC=C(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156801
title compound
Rendimiento 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156802
title compound
Rendimiento 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CCC(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156803
title compound
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)cc1
Reaction #156896
N-ethyl-4-(4-((6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3′,2′-e]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 58.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)cc1
Reaction #193937
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)c(Cl)c1
Reaction #223202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #239788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)c(F)c1
Reaction #260184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C(=O)NC2CC2)ccc1N1CCN(Cc2cnc3c(c2)NC(=O)C2CCCCN32)CC1
Reaction #375998
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(NC1CC1)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)c(Cl)c1
Reaction #403715
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)cc1
Reaction #751185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1Nc2cc(CO)cnc2N2CCCCC12
Reaction #803427
title compound
Rendimiento 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C1Nc2cc(CN3CC=C(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #803428
title compound
Rendimiento 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #803429
title compound
Rendimiento 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C1Nc2cc(CN3CCC(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #803430
title compound
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)cc1
Reaction #803526
N-ethyl-4-(4-((6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3′,2′-e]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 58.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C(NC1CC1)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CCCCN43)CC2)c(F)c1
Reaction #906098
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C1Nc2cc(CO)cnc2N2CCCCC12
Reaction #1201267
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COc1cc(C#N)ccc1N1CCN(Cc2cnc3c(c2)NC(=O)C2CCCCN32)CC1
Reaction #1210828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Página 1Siguiente