Recherche de Sous-structure

CCN1CCNCC1

CNC(=O)C(Cc1ccc2ccccc2c1)N1CCNC(CCO[Si](C)(C)C(C)(C)C)C1=O
Reaction #8626
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ncc(Cl)cc1[N+](=O)[O-]
Reaction #11769
title compound
Rendement 78.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ncc(Cl)cc1N
Reaction #11770
title compound
Rendement 86.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(C(=O)OC2C3=C(SCCS3)C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #55363
5-(4-Acetylpiperazin-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-dithiino[2,3-c]pyrrole
Rendement 38.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCNCC1.Cl
Reaction #55364
1-acetylpiperazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CCNCC1.Cl
Reaction #55365
1-propionylpiperazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CCN(C(=O)Cl)CC1
Reaction #55366
1-Chlorocarbonyl-4-propionylpiperazine
Rendement 98.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCN(c2ccc(N3CC[C@@H](OC)C3)cc2C2CCC(CC)(CC)CC2)CC1
Reaction #60518
(R)-1-butyl-4-[2-(4,4-diethylcyclohexyl)-4-(3-methoxypyrrolidin-1-yl)phenyl]piperazine
Rendement 93.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CN(CC(=O)Nc2c(Cl)cccc2Cl)CCN1CCCC(=O)C(c1ccccc1)c1ccccc1.O
Reaction #63624
3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-(4-oxo-5,5-diphenylpentyl)-1-piperazineacetamide monohydrate
Rendement 3.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(F)c1)N1CCN(Cc2ccc(Br)c(Br)c2)CC1
Reaction #68865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)N1CCN(Cc2ccc(Br)c(Br)c2)CC1)c1ccccc1
Reaction #68888
product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(N)cn3)CC2(C)C)cc1
Reaction #71426
title compound
Rendement 77.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #71427
title compound
Rendement 80.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Rendement 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3F)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78928
8
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3O)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78931
12
Rendement 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(N2CCN(CCO)CC2)ccc1[N+](=O)[O-]
Reaction #90806
5-[4-(2-Hydroxyethyl)-1-piperazinyl]-N-methyl-2-nitrobenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(N2CCN(CCO)CC2)ccc1N
Reaction #90807
2-amino-5-[4-(2-Hydroxyethyl)-1-piperazinyl]-N-methylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(C(=O)c2ccc3c(c2)cc(C(=O)N2CCS(=O)(=O)CC2)n3CC#N)CC1
Reaction #173454
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCCCC(NC(=O)C(N)Cc1cc(Cl)c(O)c(Cl)c1)C(=O)N1CCN(c2ccncc2)CC1
Reaction #177823
DOI: 10.1039/C8SC04228D
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