Busqueda de Subestructura

C1=CC(=CC=C1CCN)Cl

CCCCC(C#N)(Cn1ccnc1)c1ccc(Cl)cc1Cl.Cl
Reaction #56534
expected product
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57084
tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCC1CCCN(C(=O)C2(c3ccc(Cl)cc3)CCC2)C1
Reaction #78925
2
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N1CCN(CC2CCCN(C(=O)C3(c4ccc(Cl)cc4)CCC3)C2)CC1
Reaction #78926
3
Rendimiento 43.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3F)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78928
8
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3OC(F)(F)F)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78929
9
Rendimiento 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccccc1N1CCN(CC2CCCN(C(=O)C3(c4ccc(Cl)cc4)CCC3)C2)CC1
Reaction #78930
11
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3O)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78931
12
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #78935
oil
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(NCc1ccc2ccccc2c1)C(Cc1ccc(-c2ccccc2)cc1)c1ccc(Cl)cc1
Reaction #81144
N-{(1RS, 2RS)-3-(4-biphenylyl)-2-(4- chlorophenyl)-1-methylpropyl}-2-naphthylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(NC(C)(C)Cc3ccc(Cl)c(F)c3)c(Cl)c2)c(C)n1
Reaction #84588
title compound
Rendimiento 33.7%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2ccc(Cl)cc2Cl)cn2ccnc12
Reaction #85941
6-(2,4-Dichlorophenyl)imidazo[1,2-a]pyrazin-8(7H)-one
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cncc2c(N[C@@H](CN3CCC3)c3ccc(Cl)c(C(F)(F)F)c3)ncnc12
Reaction #88255
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Cl)cc1)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94555
3-p-chlorobenzoyl-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(CN2CC3CC3(c3ccc(Cl)cc3)C2)cc1
Reaction #94556
3-(p-Chlorobenzyl)-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1F)N1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94559
3-(o-fluorobenzoyl)-1-(p-chlorophenyl)-3-azabicyclo[3.1.0]hexane
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccccc1CN1CC2CC2(c2ccc(Cl)cc2)C1
Reaction #94560
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC[C@@H](C(=O)O)c1ccc(Cl)cc1
Reaction #169569
(S)-3-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)propanoic acid
Rendimiento 94.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC[C@@H](C(=O)O)c1ccc(Cl)cc1
Reaction #169570
(S)-3-amino-2-(4-chlorophenyl)propanoic acid hydrochloride
Rendimiento 153.3%DOI: 10.6084/m9.figshare.5104873.v1
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