2-chloro-1-[4-(4-chloro-3-methoxyphenyl)piperazin-1-yl]ethanone

COc1ccc2c(c1)oc(=O)n2CC(=O)N1CCN(c2ccc(Cl)c(OC)c2)CC1
Reaction #175835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCN(C(=O)Cn3nc(-c4cccnc4)c(Cl)c3C)CC2)ccc1Cl
Reaction #176822
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccc(C(F)(F)F)cc3)CC2)ccc1Cl
Reaction #194841
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCN(C(=O)Cn3c(=O)n(C)c4ccc(Cl)cc43)CC2)ccc1Cl
Reaction #197189
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3cccc(F)c3)CC2)ccc1Cl
Reaction #234866
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(-c2c(Cl)c(C(F)(F)F)nn2CC(=O)N2CCN(c3ccc(Cl)c(OC)c3)CC2)cc1
Reaction #262002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1c(Cl)c(C)nn1CC(=O)N1CCN(c2ccc(Cl)c(OC)c2)CC1
Reaction #263191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(N2CCN(C(=O)CN3C(=O)OCc4cc(Cl)ccc43)CC2)ccc1Cl
Reaction #269262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccccc3F)CC2)ccc1Cl
Reaction #273787
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(N2CCN(C(=O)CN3CCOCC3)CC2)ccc1Cl
Reaction #287755
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(N2CCN(C(=O)Cn3c(=O)oc4cc(F)ccc43)CC2)ccc1Cl
Reaction #292224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccccc3)CC2)ccc1Cl
Reaction #358046
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(N)c(Br)c3-c3ccccc3)CC2)ccc1Cl
Reaction #358048
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(N)c(Cl)c3C)CC2)ccc1Cl
Reaction #358049
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(-c4ccccc4)c(Br)c3C(F)(F)F)CC2)ccc1Cl
Reaction #358092
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccccc3)CC2)ccc1Cl
Reaction #358093
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(-c4cccc(F)c4)c(Cl)c3C(F)(F)F)CC2)ccc1Cl
Reaction #358094
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3cccc(F)c3)CC2)ccc1Cl
Reaction #358095
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)nc3C)CC2)ccc1Cl
Reaction #376784
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(-c2nn(CC(=O)N3CCN(c4ccc(Cl)c(OC)c4)CC3)c(C(F)(F)F)c2Cl)cc1
Reaction #398543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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