An 24 Reaktionen beteiligt

559821

CCN1CCN(c2ccc(Nc3ncc4scc(-c5ccccc5C(F)(F)F)c4n3)cn2)CC1
Reaction #213790
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #252349
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #496879
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #577260
title compound
Ausbeute 102.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #752371
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCN1CCN(c2ccc(Nc3ncc4scc(-c5cccc(N(C)S(C)(=O)=O)c5)c4n3)cn2)CC1
Reaction #1024853
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN1CCN(c2ccc(NC(=O)c3cc(NC(=O)c4ccnc(N5CCOCC5)c4)ccc3Cl)cn2)CC1
Reaction #1094317
title compound
Ausbeute 28.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
CCN1CCN(c2ccc(NC(=O)c3cc(NC(=O)c4ccnc(N5CCOCC5)c4)ccc3Cl)cn2)CC1
Reaction #1353395
title compound
Ausbeute 28.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CCN1CCN(c2ccc(NC(=O)c3ccc(C)c(NC(=O)c4csc5c(NC6CC6)ncnc45)c3)cn2)CC1
Reaction #1552201
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #1572672
compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CCN1CCN(c2ccc(Nc3nc(N)c4scc(-c5cccc(C(=O)NC)c5)c4n3)cn2)CC1
Reaction #1572673
compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CCN1CCN(c2ccc(Nc3nc(N)c4scc(-c5cccc(NS(C)(=O)=O)c5)c4n3)cn2)CC1
Reaction #1572681
compound
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CCN1CCN(c2ccc(Nc3nc(N)c4scc(-c5cnc6ccccc6c5)c4n3)cn2)CC1
Reaction #1572683
compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #2129393
compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
CCN1CCN(c2ccc(Nc3ncc4scc(-c5cccc(NS(C)(=O)=O)c5)c4n3)cn2)CC1
Reaction #2129394
compound
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
CCN1CCN(c2ccc(Nc3ncc4scc(-c5cccc(C(=O)NC6CC6)c5)c4n3)cn2)CC1
Reaction #2129403
N-Cyclopropyl-3-(2-(6-(4-ethylpiperazin-1-yl)pyridin-3-ylamino)thieno[3,2-d]pyrimidin-7-yl)benzamide
Ausbeute 51.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
CCN1CCN(c2ccc(Nc3ncc4scc(-c5cnc6ccccc6c5)c4n3)cn2)CC1
Reaction #2129410
N-(6-(4-Ethylpiperazin-1-yl)pyridin-3-yl)-7-(quinolin-3-yl)thieno[3,2-d]pyrimidin-2-amine
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
CCN1CCN(c2ccc(Nc3ncc4scc(-c5ccccc5C(F)(F)F)c4n3)cn2)CC1
Reaction #2129415
N-(6-(4-Ethylpiperazin-1-yl)pyridin-3-yl)-7-(2-(trifluoromethyl)phenyl)thieno[3,2-d]pyrimidin-2-amine
Ausbeute 61.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
CCN1CCN(c2ccc(Nc3ncc4scc(-c5cccc(N(C)S(C)(=O)=O)c5)c4n3)cn2)CC1
Reaction #2129417
N-(3-(2-(6-(4-Ethylpiperazin-1-yl)pyridin-3-ylamino)thieno[3,2-d]pyrimidin-7-yl)phenyl)-N-methylmethanesulfonamide
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
CCN1CCN(c2ccc(N)cn2)CC1
Reaction #2153909
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
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