Busqueda de Subestructura

7812

Cl.Cl.OC(NC1CCCCC1)=[SH]CCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3892
N-cyclohexyl-S-{3-[4-(4-chlorobenzyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Rendimiento 100.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.OC(Nc1ccccc1)=[SH]CCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3930
N-phenyl-S-{2-[4-(4-chlorobenzyl)piperazin-1-yl]ethyl}thiocarbamate dihydrochloride
Rendimiento 128.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCNC(O)=[SH]CCCN1CCN(Cc2ccc(Cl)cc2)CC1.Cl.Cl
Reaction #3933
N-(n-hexyl)-S-{3-[4-(4-chlorobenzyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Rendimiento 157.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(O)=[SH]CCCN1CCN(Cc2ccc(Cl)cc2)CC1.CC(C)(C)NC(O)=[SH]CCCN1CCN(Cc2ccc(Cl)cc2)CC1.Cl.Cl.Cl.Cl.O.O.O
Reaction #3943
N-(t-butyl)-S-{3-[4-(4-chlorobenzyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride sesquihydrate
Rendimiento 140.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCN(CCCN2CCN(Cc3ccc(Cl)cc3)CC2)CC1)c1ccccc1
Reaction #4411
1-[4-(4-chlorobenzyl)-1-piperazinyl]-3-(4-phenacyl-1-piperazinyl)propane
Rendimiento 77.5%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
Cl.Cl.Cl.Cl.O=C(O)C(CN1CCN(CCCN2CCN(Cc3ccc(Cl)cc3)CC2)CC1)c1ccccc1
Reaction #4417
1-[4-(4-chlorobenzyl)-1-piperazinyl]-3-[4-(2-carboxy-2-phenylethyl)-1-piperazinyl]propane tetrahydrochloride
Rendimiento 172.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)CCc1cccnc1C2N1CCN(Cc2ccncc2)CC1
Reaction #49693
(+)-8-chloro-6,11-dihydro-11-[4-(4-pyridinylmethyl)-1-piperazinyl]-5h-benzo[5,6]cyclohepta-[1,2-b]pyridine
Rendimiento 75.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)CCc1cccnc1C2N1CCN(Cc2ccncc2)CC1
Reaction #49694
(-)-8-chloro-6,11-dihydro-11-[4 -(4-pyridinylmethyl)-1-piperazinyl]-5h-benzo[5,6]cyclohepta-[1,2-b]pyridine
Rendimiento 45.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)c(C)c(C)c2cc1OCCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #50606
6-{3-[4-(4-chlorophenylmethyl)-1-piperazinyl]-propoxy}-7-methoxy-3,4-dimethyl-2H-1-benzopyran-2-one
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N1CCN(Cc2ccc(Cl)c(Cl)c2)CC1
Reaction #68885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #75628
title compound
Rendimiento 84.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #75629
title compound
Rendimiento 112.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #75630
title compound
Rendimiento 85.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CCNCC1)N1CCN(C2c3ccc(Cl)cc3CCc3cc(Br)cnc32)CC1
Reaction #75631
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #91866
solid
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)cc1-c1nc2c(N3CCN(Cc4ccc(Cl)cc4)CC3)c(Cl)cnc2[nH]1
Reaction #91867
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cc(CN2CCN(C(c3ccccc3)c3ccc(Cl)cc3)CC2)ccc1O
Reaction #187728
DOI: 10.1039/C8SC04228D
NC(=O)c1ccc2[nH]c(-c3ccc(C(c4ccc(Cl)cc4)N4CCNCC4)cc3)nc2c1
Reaction #189514
DOI: 10.1039/C8SC04228D
Nc1ncc(Br)c(N2CCN(Cc3ccc(Cl)cc3)CC2)c1[N+](=O)[O-]
Reaction #201603
DOI: 10.1039/C8SC04228D
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