4-ethylpiperidine

CCC1CCN(C(=O)C(CCCNC(=O)OCc2ccccc2)NS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1
Reaction #6464
3d
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC1CCN(Cc2ccc(COc3cccc4c3CN(C(CCC(=O)OC)C(N)=O)C4=O)cc2)CC1
Reaction #198017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1CCN(C(=O)C(CCCC2CCN(C(=O)OCc3ccccc3)CC2)NC(=O)OC(C)(C)C)CC1
Reaction #227453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC1CCNCC1C(=O)C(CCCc1ccc(N)nc1)NC(=O)OC(C)(C)C
Reaction #274853
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1CCN(CC#N)CC1
Reaction #288353
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1CCN(C(=O)C(CCCNC(=O)OCc2ccccc2)NS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1
Reaction #784835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCC1CCN(c2nc(-c3ccc(OC)cc3)cc3ccccc23)CC1.Cl
Reaction #1094137
title compound
Ausbeute 15.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
CCC1CCN(c2nc(-c3ccc(OC)cc3)cc3ccccc23)CC1.Cl
Reaction #1338373
title compound
Ausbeute 15.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_01
CCC1CCN(CC#N)CC1
Reaction #1728217
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02