Substructure Search

540

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
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
Yield 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
Yield 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
Yield 3.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(N)cn3)CC2(C)C)cc1
Reaction #71426
title compound
Yield 77.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc([N+](=O)[O-])cn3)CC2(C)C)cc1
Reaction #71427
title compound
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3F)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78928
8
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3O)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78931
12
Yield 32.0%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
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #179112
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)N(CC)CC)c3ccccc3)CC2)c(C#C[Si](C)(C)C)c1
Reaction #183673
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(C(=O)c2ccc3[nH]c(C(=O)N4CCN(S(=O)(=O)N5CCCCC5)CC4)cc3c2)CC1
Reaction #185009
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(C(=O)c2ccc3c(c2)cc(C(=O)N2CCN(C(=O)C4CC4)CC2)n3-c2ccc(Cl)nc2)CC1
Reaction #187101
DOI: 10.1039/C8SC04228D
O=C(NO)C(O)CC(=O)N1CCN(c2ccc(F)cc2)CC1
Reaction #187677
DOI: 10.1039/C8SC04228D
O=C(NCC1CC1)Nc1ccc(C(=O)N2CCN(Cc3ccc(C(O)(C(F)(F)F)C(F)(F)F)cc3)CC2C(=O)O)cc1
Reaction #187769
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCc1cc(Cl)c(NC(=O)CN2CCN(CCCCC(c3ccc(F)cc3)c3ccc(F)cc3)CC2C(N)=O)c(Cl)c1
Reaction #196096
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(C(=O)c2ccc3[nH]c(C(=O)N4CCN(S(C)(=O)=O)CC4)cc3c2)CC1
Reaction #197572
DOI: 10.1039/C8SC04228D
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