#794718

Clc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1Cl
Reaction #8758
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NC(=O)c1cccc2c(NCc3ccc(Cl)c(Cl)c3)nnnc12
Reaction #88239
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(Cl)c(Cl)c1
Reaction #91325
title compound
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccncc1NCc1ccc(Cl)c(Cl)c1
Reaction #91326
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(NCc2ccc(Cl)c(Cl)c2)nc1
Reaction #164624
methyl 6-(3,4-dichlorobenzylamino)nicotinate
Rendimiento 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOc1cc2ncc(C#N)c(NCc3ccc(Cl)c(Cl)c3)c2cc1OCC
Reaction #173059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1sc2nc(-c3cccnc3)nc(NCc3ccc(Cl)c(Cl)c3)c2c1C
Reaction #173468
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(-c3cccnc3)nc2s1
Reaction #177925
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(Cl)nc2s1
Reaction #184175
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(Cl)nc2s1
Reaction #192989
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCc1ccc(Cl)c(Cl)c1)Nc1cccc2cnccc12
Reaction #197736
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1Cl
Reaction #199008
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(-c3ccncc3)nc2s1
Reaction #200776
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(-c2nc(NCc3ccc(Cl)c(Cl)c3)c3c(C)c(C)sc3n2)cc1
Reaction #206542
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1csc2nc(-c3ccno3)nc(NCc3ccc(Cl)c(Cl)c3)c12
Reaction #210835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccc2c(-c3ccc(OCCCNCc4ccc(Cl)c(Cl)c4)cc3)noc2c1
Reaction #225271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1sc2nc(-c3ccncc3)nc(NCc3ccc(Cl)c(Cl)c3)c2c1C
Reaction #228468
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(-c3ccno3)nc2s1
Reaction #232090
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
FC(F)(F)c1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(-c3cnccn3)nc2s1
Reaction #237017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
FC(F)(F)c1cc2c(NCc3ccc(Cl)c(Cl)c3)nc(-c3ccno3)nc2s1
Reaction #238682
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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