Recherche de Sous-structure

CN(CCN)CCc1ccccc1

CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Reaction #5498
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2ccccc2)CC1Cc1ccc2ccccc2c1
Reaction #10273
4-benzyl-2-(naphthalen-2-ylmethyl)piperazine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CCNC(Cc3ccc4ccccc4c3)C2)cc1
Reaction #10274
1-benzyl-3-(naphthalen-2-ylmethyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(NC(=O)C(C)(C)C)c4)CC3)cccc2n1
Reaction #44067
title compound
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Reaction #50252
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)N2C(=O)OC[C@H]2Cc2ccccc2)NC1=O
Reaction #50253
N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-(R)-4-benzyl-2-oxazolidinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2cccc(-c3ccc(Cl)c(Cl)c3)c2)C2(O)CCCCC2)CC1
Reaction #57094
tert-butyl 4-[2-(3′,4′-dichloro-biphenyl-3-yl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.OC1(C(CN2CCNCC2)c2cccc(-c3ccc(Cl)c(Cl)c3)c2)CCCCC1
Reaction #57095
1-[1-(3′,4′-dichloro-1,1′-biphenyl-3-yl)-2-piperazin-1-ylethyl]cyclohexanol dihydrochloride
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2ccc(Oc3cccc4ccccc34)cc2)C2(O)CCCCC2)CC1
Reaction #57121
tert-butyl 4-{2-(1-hydroxycyclohexyl)-2-[4-(1-naphthyloxy)phenyl]ethyl}piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC(N(CCNC(=O)c2ccccc2)CCc2ccc(Cl)cc2)CC1
Reaction #88065
Allyl 4-((2-benzamidoethyl)(4-chlorophenethyl)amino)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCN(CCc1ccc(Cl)cc1)C1CCNCC1)c1ccccc1
Reaction #88066
N-(2-((4-chlorophenethyl)(piperidin-4-yl)amino)ethyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@@H](C(=O)N1CCN(c2c(-c3ccccc3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1)C(=O)OC(C)(C)C
Reaction #166728
(S)-tert-butyl 2-(4-chlorophenyl)-3-oxo-3-(4-(5-phenyl-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)propyl(isopropyl)carbamate
Rendement 2.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](C(=O)N1CCN(c2c(-c3ccccc3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1
Reaction #166729
(S)-2-(4-chlorophenyl)-3-(isopropylamino)-1-(4-(5-phenyl-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)propan-1-one
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@@H](C(=O)N1CCN(c2c(-c3cccnc3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1)C(=O)OC(C)(C)C
Reaction #166757
(S)-tert-butyl 2-(4-chlorophenyl)-3-oxo-3-(4-(5-(pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)propyl(isopropyl)carbamate
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](C(=O)N1CCN(c2c(-c3cccnc3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1
Reaction #166758
(S)-2-(4-chlorophenyl)-3-(isopropylamino)-1-(4-(5-(pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)propan-1-one
Rendement 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@@H](C(=O)N1CCN(c2c(-c3ccc(F)cc3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1)C(=O)OC(C)(C)C
Reaction #166763
(S)-tert-butyl 2-(4-chlorophenyl)-3-(4-(5-(4-fluorophenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)-3-oxopropyl(isopropyl)carbamate
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC[C@@H](C(=O)N1CCN(c2c(-c3ccc(F)cc3)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1
Reaction #166764
(S)-2-(4-chlorophenyl)-1-(4-(5-(4-fluorophenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)-3-(isopropylamino)propan-1-one
Rendement 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@@H](C(=O)N1CCN(c2c(-c3ccccc3F)cnc3[nH]ccc23)CC1)c1ccc(Cl)cc1)C(=O)OC(C)(C)C
Reaction #166780
tert-butyl (2S)-2-(4-chlorophenyl)-3-(4-(5-(2-fluorophenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)-3-oxopropyl(isopropyl)carbamate
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
[Cl-]
Reaction #173669
DOI: 10.1039/C8SC04228D
CNC(=O)C(Cc1ccccc1)N(C)C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CC1CN(C(=O)OC(C)(C)C)C1
Reaction #179160
DOI: 10.1039/C8SC04228D
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