4-piperazinoindole

C[C@H](CN1CCN(c2cccc3[nH]ccc23)CC1)Nc1ccccn1
Reaction #991
(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc2c(C3CCC(N4CCN(c5cccc6[nH]ccc56)CC4)CC3)c[nH]c2c1
Reaction #176321
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CNC(Cc1ccccn1)C(=O)N1CCN(c2cccc3[nH]ccc23)CC1
Reaction #192170
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2[nH]cc(C3CCC(N4CCN(c5cccc6[nH]ccc56)CC4)CC3)c2c1
Reaction #193019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC(COc1ccccc1Cl)CN1CCN(c2cccc3[nH]ccc23)CC1
Reaction #202867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2c(c1)CC(CCN1CCN(c3cccc4[nH]ccc34)CC1)C2
Reaction #362900
title compound
Rendimiento 47.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
c1ccc(C(CCN2CCN(c3cccc4[nH]ccc34)CC2)c2ccccn2)nc1
Reaction #382112
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ccc(OCC(O)CN2CCN(c3cccc4[nH]ccc34)CC2)cc1
Reaction #405613
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1Cc2c(ccc3c2OC(CN2CCN(c4cccc5[nH]ccc45)CC2)CO3)N1
Reaction #449431
title compound
Rendimiento 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
C[C@H](CN1CCN(c2cccc3[nH]ccc23)CC1)Nc1ccccn1
Reaction #455885
(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
OC(COc1ccc(F)cc1)CN1CCN(c2cccc3[nH]ccc23)CC1
Reaction #469445
solid
Rendimiento 99.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
c1cc(N2CCN([C@H]3CC[C@@H](c4c[nH]c5ccccc54)CC3)CC2)c2cc[nH]c2c1
Reaction #515737
product
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
Fc1cccc2[nH]cc([C@H]3CC[C@@H](N4CCN(c5cccc6[nH]ccc56)CC4)CC3)c12
Reaction #515738
product
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
COc1ccc2[nH]cc([C@H]3CC[C@@H](N4CCN(c5cccc6[nH]ccc56)CC4)CC3)c2c1
Reaction #515739
product
Rendimiento 55.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
Cc1[nH]c2ccccc2c1[C@H]1CC[C@@H](N2CCN(c3cccc4[nH]ccc34)CC2)CC1
Reaction #515740
white solid
Rendimiento 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
Cn1cc(C2CCC(N3CCN(c4cccc5[nH]ccc45)CC3)CC2)c2cc(C#N)ccc21
Reaction #515741
product
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCCn1cc(C2CCC(N3CCN(c4cccc5[nH]ccc45)CC3)CC2)c2cc(C#N)ccc21
Reaction #515742
product
Rendimiento 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)n1cc(C2CCC(N3CCN(c4cccc5[nH]ccc45)CC3)CC2)c2cc(C#N)ccc21
Reaction #515743
product
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
C[C@H](CN1CCN(c2cccc3[nH]ccc23)CC1)Nc1ccccn1
Reaction #653775
(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
SCCN1CCN(c2cccc3[nH]ccc23)CC1
Reaction #774766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
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