1-(4-chlorobenzyl)piperazine

Cl.Cl.ClCCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3888
1-(4-chlorobenzyl)-4-(3-chloropropyl)piperazine dihydrochloride
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cl.Cl.ClCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3928
1-(4-chlorobenzyl)-4-(2-chloroethyl)piperazine dihydrochloride
Rendimiento 112.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cl.Cl.O.O=C(CC(=O)N1CCN(Cc2ccc(Cl)cc2)CC1)N1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #4412
1,3-bis[4-(4 -chlorobenzyl)-1-piperazinyl]-1,3-dioxopropane dihydrochloride monohydrate
Rendimiento 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #91866
solid
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1cn(CC)c2nc(N3CCN(Cc4ccc(Cl)cc4)CC3)ncc2c1=O
Reaction #94287
2-(4'-p-chlorobenzyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Nc1ncc(Br)c(N2CCN(Cc3ccc(Cl)cc3)CC2)c1[N+](=O)[O-]
Reaction #201603
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #460019
ethyl 3-[4-(4-chlorobenzyl)-piperazin-1-yl]-propionate
Rendimiento 92.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
N=c1n(CCCOc2ccc(F)cc2)c2ccccc2n1Cc1ccc(N2CCN(Cc3ccc(Cl)cc3)CC2)cc1
Reaction #497520
1-{4-[4-(4-chloro-benzyl)-piperazin-1-yl]-benzyl}-3-[3-(4-fluoro-phenoxy)-propyl]-1,3-dihydro-benzoimidazol-2-ylideneamine
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
N=c1n(CCCOc2ccc(F)cc2)c2ccccc2n1Cc1ccc(CN2CCN(Cc3ccc(Cl)cc3)CC2)cc1
Reaction #497531
1-{4-[4-(4-chloro-benzyl)-piperazin-1-ylmethyl]-benzyl}-3-[3-(4-fluoro-phenoxy)-propyl]-1,3-dihydro-benzoimidazol-2-ylideneamine
Rendimiento 11.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
—
Reaction #503916
solid
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
—
Reaction #503934
solid
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
ClCCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #531393
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
O=c1cc(OCc2ccccc2)c2ccc(OCC(O)CN3CCN(Cc4ccc(Cl)cc4)CC3)cc2o1
Reaction #531397
title compound
Rendimiento 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
C=CCc1c(OCC(O)CN2CCN(Cc3ccc(Cl)cc3)CC2)ccc2c(OCc3ccccc3)cc(=O)oc12
Reaction #531400
title compound
Rendimiento 52.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
ClCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #531402
title compound
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
O=C(NCc1ccc(Cl)cc1)N1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #575578
1-(((4-chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazine
Rendimiento 54.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
O=C(NCc1ccc(Cl)cc1)N1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #576387
1-(((4-chlorobenzyl)amino)carbonyl)-4-(4-chlorobenzyl)piperazine
Rendimiento 54.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
CC(C)(C)c1ccc(NC(=O)NCCCN2CCN(Cc3ccc(Cl)cc3)CC2)cc1.Cl.Cl
Reaction #630380
title compound
Rendimiento 108.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
O=C(c1cccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)c1)N1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #746680
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #746728
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
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