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7805

Cl.Cl.ClCCCN1CCN(CCc2ccc(Cl)cc2)CC1
Reaction #3914
1-(4-chlorophenethyl)-4-(3-chloropropyl)piperazine dihydrochloride
Выход 118.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.SCCCN1CCN(CCc2ccc(Cl)cc2)CC1
Reaction #3915
3-[4-(4-chlorophenethyl)piperazin-1-yl]propanethiol dihydrochloride
Выход 176.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O.OC(Nc1ccccc1)=[SH]CCCN1CCN(CCc2ccc(Cl)cc2)CC1
Reaction #3916
N-phenyl-S-{3-[4-(4-chlorophenethyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride monohydrate
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(NC(O)=[SH]CCCN2CCN(CCc3ccc(Cl)cc3)CC2)cc1.Cl.Cl
Reaction #3917
N-(4-n-butylphenyl)-S-{3-[4-(4-chlorophenethyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Выход 49.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(O)=[SH]CCCN2CCN(CCc3ccc(Cl)cc3)CC2)cc1.Cl.Cl
Reaction #3918
N-(4-methoxyphenyl)-S-{3-[4-(4-chlorophenethyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Выход 49.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.OC(NC1CCCCC1)=[SH]CCCN1CCN(CCc2ccc(Cl)cc2)CC1
Reaction #3931
N-cyclohexyl-S-{3-[4-(4-chlorophenethyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Выход 170.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(=O)c2ccc(Cl)cc2Cl)CC1
Reaction #60053
tert-butyl 4-[2-(2,4-dichlorophenyl)-2-oxoethyl]piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C(=O)c1ccc(Cl)cc1Cl)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60054
tert-butyl 4-{2-(2,4-dichlorophenyl)-1-[(dimethylamino)methylene]-2-oxoethyl}piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(=O)c2ccc(Cl)cc2Cl)CC1
Reaction #60064
tert-butyl 4-[2-(2,4-dichlorophenyl)-2-oxoethyl]piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C(=O)c1ccc(Cl)cc1Cl)N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60065
tert-butyl 4-{2-(2,4-dichlorophenyl)-1-[(dimethylamino)methylene]-2-oxo-ethyl}piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1cccc(Cl)c1CN1CCN(C(=O)Cc2ccc(Cl)cc2)CC1
Reaction #66536
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc1ccc(Cl)cc1
Reaction #66548
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2ccc(Cl)cc2)c2ccc(Cl)cc2)CC1
Reaction #73783
title compound
Выход 11.1%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C(CN2CCNCC2)c2ccc(Cl)cc2)cc1
Reaction #73784
HCl
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C(CN2CCNCC2)c2ccc(-c3cn[nH]c3)cc2)cc1
Reaction #73785
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C(CN2CCCCC2)c2ccc(-c3cn[nH]c3)cc2)cc1
Reaction #73786
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@@H](O)c2ncnc(N3CCN(C(=O)[C@H](CNCC(C)(C)O)c4ccc(Cl)cc4)CC3)c21
Reaction #162588
(S)-2-(4-chlorophenyl)-3-(2-hydroxy -2-methylpropylamino)-1-(4-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)propan-1-one
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](C(=O)N1CCN(c2c(-c3cccc(F)c3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1
Reaction #166712
(S)-2-(4-chlorophenyl)-1-(4-(5-(3-fluorophenyl)-1H-pyrrolo[2,3-b]pyri din-4-yl)piperazin-1-yl)-3-(isopropylamino)propan-1-one
Выход 60.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cnc3[nH]ccc3c2N2CCN(C(=O)[C@H](CNC(C)C)c3ccc(Cl)cc3)CC2)c1
Reaction #166719
(S)-2-(4-chlorophenyl)-3-(isopropylamino)-1-(4-(5-(3-methoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)propan-1-one
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3[nH]ccc3c2N2CCN(C(=O)[C@H](CN(C(=O)OC(C)(C)C)C(C)C)c3ccc(Cl)cc3)CC2)cc1OC
Reaction #166722
(S)-tert-butyl 2-(4-chlorophenyl)-3-(4-(5-(3,4-dimethoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)-3-oxopropyl(isopropyl)carbamate
Выход 18.3%DOI: 10.6084/m9.figshare.5104873.v1
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