#6803951

Clc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8742
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1ccc(CNCCOc2cccc(-c3noc4ccsc34)c2)cc1
Reaction #8755
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(CO)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51895
title compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1c(CO)sc2c(O)c(C(=O)NCc3ccc(Cl)cc3)cnc12
Reaction #51900
title compound
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCOCc1csc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51916
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CC[C@@H](CC(=O)NCc1ccc(Cl)cc1)C(=O)N1C(=O)OC[C@H]1Cc1ccccc1
Reaction #69347
4a
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(C[C@@H]1C/C=C/CCC(=O)N[C@H](c2ccccc2)COC1=O)NCc1ccc(Cl)cc1
Reaction #69355
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nc(N)sc1C(=O)NCc1ccc(Cl)cc1
Reaction #73588
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)C1OC(NCc2ccc(Cl)cc2)=NC1=O
Reaction #74365
2-[(4-chlorobenzyl)amino]-5-isopropyl-1,3-oxazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)O.Nc1cc2ncnc(NCc3ccc(Cl)cc3)c2cn1
Reaction #79088
7-Amino-4-(4-chlorobenzylamino)pyrido[4,3-d]pyrimidine Mesylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(NCc1ccc(Cl)cc1)c1cnc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2c1
Reaction #80218
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)N[C@H](CCCNC(N)=N[N+](=O)[O-])C(=O)NCc1ccc(Cl)cc1
Reaction #80857
(R)-N-[(4-Chlorophenyl) methyl]-N5 -[amino (nitroimino) methyl]-N2 -(tert. -butoxycarbonyl)-ornithinamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=[N+]([O-])c1cccnc1NCc1ccc(Cl)cc1
Reaction #83776
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1n[nH]c(N)c1-c1nc2ccc(S(=O)(=O)NCc3ccc(Cl)cc3)cc2s1
Reaction #85530
title compound
Ausbeute 16.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1ccncc1NCc1ccc(Cl)cc1
Reaction #91320
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccncc1NCc1ccc(Cl)cc1
Reaction #91321
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1OCCC1=CNCc1ccc(Cl)cc1
Reaction #167516
3-(4-chlorobenzylamino)methylenedihydrofuran-2-one
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN(CC)CCNCc1ccc(Cl)cc1
Reaction #168190
N1-(4-chlorobenzyl)-N2,N2-diethylethane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1ccc(CNc2nc(Cl)nc3nc[nH]c23)cc1
Reaction #175583
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2c(Cl)cc(Br)cc2CN1Cc1ccc(Cl)cc1
Reaction #177280
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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