4-(piperazin-1-yl)anisole

COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2303
4-[4-(4-pyridyl)-piperazin-1-yl]anisole
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(N2CCN(Cc3oc(-c4ccc(C(F)(F)F)cc4)cc3CO)CC2)cc1
Reaction #9784
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(N2CCN(C(=O)CC(OC(=O)N(C)C)c3ccccc3)CC2)cc1
Reaction #72488
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(N2CCN(CCC3CN(C)C(=O)O3)CC2)cc1
Reaction #174296
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(C(=O)Nc3nc4cc(Cl)ccc4nc3OC)CC2)cc1
Reaction #176255
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(CCCc3cc(-c4ccc(F)cc4)n(-c4ccccc4)n3)CC2)cc1
Reaction #179990
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(Cc3nc4ccccc4[nH]3)CC2)cc1
Reaction #183236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(C(=O)OCCN3CCN(C)CC3)CC2)cc1
Reaction #184368
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cc(N2CCN(CCCC3CCCCC3)CC2)ccc1OCc1ccccc1
Reaction #188202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(CCCc3cc(-c4cccs4)n(C(C)(C)C)n3)CC2)cc1
Reaction #191793
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(Cc3cnc(Cc4ccc(OC)c(OC)c4)c4cc(OC)c(OC)cc34)CC2)cc1
Reaction #195045
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(c3ccc([N+](=O)[O-])cc3)CC2)cc1
Reaction #195789
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(C(=O)Nc3nc4cc(OC)ccc4nc3OC)CC2)cc1
Reaction #199721
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCS(=O)(=O)N1CCN(c2cc(F)c(OC)cc2F)CC1
Reaction #200038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1cc(CCCN2CCN(c3ccc(OC)cc3)CC2)nn1-c1ccccc1
Reaction #205840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(c3cc4c(c(C)c3C)OC(C)(C)C4)CC2)cc1
Reaction #207470
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C)CC2)cc1
Reaction #221634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(N2CCN(C(=O)c3cccc(-c4ccc(OC)c(OC)c4)n3)CC2)cc1
Reaction #222246
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(N2CCN(c3cc4c(cc3-c3cccnc3)OC(C)(C)C4)CC2)cc1
Reaction #237849
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(N2CCN(N=O)CC2)cc1
Reaction #253286
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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