(4-methylphenyl)methanamine

Cc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8757
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8781
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(CN2Cc3c(Cl)nnc(Cl)c3C2)cc1
Reaction #70503
solid
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(CNc2ccc3nc[nH]c3c2)cc1
Reaction #74208
N-(4-Methylbenzyl)-3H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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.v1uspto-grants-2004_03
Cc1ccc(CNC(=O)c2cnc3cc(NC(=O)c4ccccc4-c4ccc(C(F)(F)F)cc4)ccc3c2)cc1
Reaction #80219
title compound
収率 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91335
title compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(CNc2nc(Cl)nc(NC3NC(=O)N(C)C3=O)n2)cc1
Reaction #163519
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(CNC(=O)C2=C(C(=O)Nc3cc(OC4CCCC4)c(Cl)cc3F)CCCC2)cc1
Reaction #188557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1nc(C(=O)NCc2ccc(C)cc2)cc(N)c1C#N
Reaction #201214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(CNC(=O)c2ccc3n2Cc2ccccc2N(C(=O)CSc2ccc(Br)cc2)C3)cc1
Reaction #201608
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(CNC(=O)c2ccc(-c3cc(-c4nnc(C)o4)ccc3C)cc2)cc1
Reaction #218870
2′-Methyl-N-(4-methylbenzyl)-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Cc1ccc(CNC(=O)Cn2ncc3cc(-c4cc(C(=O)NC5CC5)cc(F)c4C)ccc32)cc1
Reaction #221762
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCn1c(C)c(C)c2cc(C(=O)NCc3ccc(C)cc3)nc(N3CCc4ccccc4C3)c21
Reaction #223951
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #246351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(CNC(=O)Cn2ncc3cc(-c4cc(C(=O)NC5CC5)ccc4C)ccc32)cc1
Reaction #255188
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #257887
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(CNc2nccc3c(C)c(C)n(Cc4ccccc4)c23)cc1
Reaction #273355
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(CN=C(NC#N)c2cccnc2)cc1
Reaction #283255
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1c(NCc2ccc(C)cc2)cnn(C(C)(C)C)c1=O
Reaction #302680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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