Recherche de Sous-structure

623197

CCO[C@@H]1CNCC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1.Cl
Reaction #71995
title compound
Rendement 231.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccccn2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71996
title compound
Rendement 3.5%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)C(=O)OC)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71997
title compound
Rendement 90.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2nccs2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71998
title compound
Rendement 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2nc3ccccc3s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71999
title compound
Rendement 64.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ncccn2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72001
title compound
Rendement 22.3%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccn(C)c(=O)c2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72002
title compound
Rendement 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)C(N)=O)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72003
title compound
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2cc[nH]c(=O)c2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72004
title compound
Rendement 5.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-n2ccc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](OCC)C3)cc2=O)nc1C
Reaction #72006
title compound
Rendement 6.5%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)C(=O)c2ccccc2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72008
title compound
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)c2cscn2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72009
title compound
Rendement 42.2%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)C(=O)Nc2ccccc2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72010
title compound
Rendement 48.3%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72011
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc2nc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](OC(C)C)C3)sc12
Reaction #72018
title compound
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC(C)C)C2)nc1C(=O)NCCOC
Reaction #72020
title compound
Rendement 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2nncs2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72022
title compound
Rendement 37.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CNCC[C@@H]1NC(=O)c1nc(CC)c(Cl)[nH]1
Reaction #72025
cis(±)-4-{[(5-chloro-4-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-ethoxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CNCC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1.Cl
Reaction #1512374
title compound
Rendement 231.7%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccccn2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #1512375
title compound
Rendement 3.5%DOI: 10.6084/m9.figshare.5104873.v1
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