#NCCc1ccc(N)cc1

CS(=O)(=O)N(CCCN)Cc1cccc(-c2ccnc(NCCc3ccc(N)cc3)n2)c1
Reaction #42983
N-(3-{2-[2-(4-Amino-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-N-(3-amino-propyl)-methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #53414
83
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #168495
83
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(CCNC(=O)OCc2ccccc2)cc1
Reaction #186058
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(cc1OC)CN(CCc1ccc(N)cc1)C2
Reaction #213085
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1c(C)nc2cccc(NCCc3ccc(N)cc3)n12
Reaction #249731
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ccc(CCNc2ncnc3ccsc23)cc1
Reaction #268265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(C)cc(C(CN)c2ccc(N)cc2)c1
Reaction #274553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #305103
83
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
NCCc1ccc(NC[C@H](O)c2ccccc2)cc1
Reaction #313461
product 2
المردود 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
N#CNC(=NCCc1ccc(N)cc1)c1cccnc1
Reaction #414295
N-cyano-N'-[2-(4-aminophenyl)ethyl]-3-pyridinecarboximidamide
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
F[B-](F)(F)F.F[B-](F)(F)F.N#[N+]c1ccc(CC[NH3+])cc1
Reaction #426619
powder
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOCC.CO.N=C(N)c1ccccn1
Reaction #461344
methanol diethyl ether pyridinecarboximidamide
المردود 124.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #544415
83
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #544781
83
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
NCCc1ccc(NC[C@H](O)c2ccccc2)cc1
Reaction #589176
product 2
المردود 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
Nc1ccc(CCn2c(=O)c3cccc4ncc(c2=O)n43)cc1
Reaction #706699
desired compound
المردود 33.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CCOC(=O)c1c(C)nc2cccc(NCCc3ccc(N)cc3)n12
Reaction #706712
desired compound
المردود 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CC(C)(C)[Si](C)(C)OC(CNCCc1ccc(N)cc1)c1ccc(OCc2ccccc2)c2[nH]c(=O)ccc12
Reaction #754266
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
NCCc1ccc(NCC(O)c2ccccc2)cc1
Reaction #789360
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
الصفحة 1التالي