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Cc1ccc(CCN)cc1

Cc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8757
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8781
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
Cc1ccc(CCNc2nccc(-c3cccc(CN(CCCN)S(C)(=O)=O)c3)n2)cc1
Reaction #42998
N-(3-Amino-propyl)-N-{3-[2-(2-p-tolyl-ethylamino)-pyrimidin-4-yl]-benzyl}-methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N(CCCN)Cc1cccc(-c2ccnc(NCCc3ccc(Cl)cc3)n2)c1
Reaction #43006
N-(3-Amino-propyl)-N-(3-{2-[2-(4-chloro-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #53414
83
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CCNC(=O)c2ccncc2Nc2ccc(I)cc2F)cc1
Reaction #67858
3-[(2-fluoro-4-iodophenyl)amino]-N-[2-(4-methylphenyl)ethyl]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2Cc3c(Cl)nnc(Cl)c3C2)cc1
Reaction #70503
solid
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNc2ccc3nc[nH]c3c2)cc1
Reaction #74208
N-(4-Methylbenzyl)-3H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
NCCc1ccc(CCN)cc1
Reaction #76641
2-[4-(2-aminoethyl)phenyl]ethylamine
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCC1CCC(CCN)CC1
Reaction #76665
2-[4-(2-aminoethyl)cyclohexyl]ethylamine
Выход 339.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC2c3cc(OC)c(OC)cc3CCN2CC(=O)NCc2ccc(C)cc2)cc1OC
Reaction #76899
2-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(4-methyl-benzyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccc(Cl)cc1)c1ncccc1O
Reaction #77727
title compound
Выход 70.5%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CNCCc1ccc(Cl)cc1
Reaction #78251
compound
Выход 49.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)c2cnc3cc(NC(=O)c4ccccc4-c4ccc(C(F)(F)F)cc4)ccc3c2)cc1
Reaction #80219
title compound
Выход 40.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccc(Cl)cc1)c1cc([N+](=O)[O-])[nH]n1
Reaction #86073
5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amide
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(CCc2ccc(Cl)cc2)C2CCN(C(=O)OC(C)(C)C)CC2)cc1
Reaction #88073
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91335
title compound
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1nc(C2CCCC(Nc3c(NCCc4ccc(Cl)cc4)c(=O)c3=O)C2)cs1
Reaction #94856
1-[3-(2-guanidinothiazol-4-yl)cyclohexylamino]-2-[2-(p-chlorophenyl)ethylamino]cyclobutene-3,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNc2nc(Cl)nc(NC3NC(=O)N(C)C3=O)n2)cc1
Reaction #163519
crude product
DOI: 10.6084/m9.figshare.5104873.v1
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