4-(N-tert-butyloxycarbonylaminomethyl) piperidine

CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #954
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCN1CCC(CNC(=O)OC(C)(C)C)CC1
Reaction #44860
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C1(CN2CCC(CNC(=O)OC(C)(C)C)CC2)CCCC1
Reaction #44867
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NCC1CCN(CC(C)(C)C(=O)OCc2ccccc2)CC1
Reaction #44880
title compound
Ausbeute 1.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NCC1CCN(C#N)CC1
Reaction #222826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C2OCCOC2CN2CCC(CNC(=O)OC(C)(C)C)CC2)cc1
Reaction #269074
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NCC1CCN(C(=O)C2CC2c2ccccc2)CC1
Reaction #295472
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NCC1CCN(c2nc(Cl)nc3ccoc23)CC1
Reaction #295984
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(N2CCOCC2)c2sc(NC(=O)N3CCC(CNS(C)(=O)=O)CC3)nc12
Reaction #300764
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NCC1CCN(c2cc(F)cc3ccc(-c4nnc5ccccn45)nc23)CC1
Reaction #371881
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)n1ncc([N+](=O)[O-])c1N1CCC(CNC(=O)OC(C)(C)C)CC1
Reaction #378714
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)NCC1CCN(c2nsnc2Cl)CC1
Reaction #381320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)NCC1CCN(c2cccc3ccc(C4COC(C)(C)O4)nc23)CC1
Reaction #426853
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)NCC1CCN(c2cccc3ccc(C=O)nc23)CC1
Reaction #426862
tert-butyl(1-(2-formylquinolin-8-yl)piperidin-4-yl)methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)NCC1CCN(c2cc(F)cc3ccc(-c4nnc5ccccn45)nc23)CC1
Reaction #426871
tert-butyl(1-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-6-fluoroquinolin-8-yl)piperidin-4-yl)methylcarbamate
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #428981
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COc1ccc(C2OCCOC2CN2CCC(CNC(=O)OC(C)(C)C)CC2)cc1
Reaction #431466
1-(3-ethylenedioxy-3-(4-methoxyphenyl)propyl)-4-(tert-butoxycarbonylaminomethyl)piperidine
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COc1ccc(C2OCCOC2CCN2CCC(CNC(=O)OC(C)(C)C)CC2)cc1
Reaction #431467
1-(4-ethylenedioxy-4-(4-methoxyphenyl)butyl)-4-(tert-butoxycarbonylaminomethyl)piperidine
Ausbeute 37.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
NCC1CCN(c2cc(Nc3cnccn3)ncn2)CC1
Reaction #471806
N-(6-(4-(aminomethyl)piperidin-1-yl)pyrimidin-4-yl)pyrazin-2-amine
Ausbeute 16.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)OC(=O)NCC1CCN(CC#N)CC1
Reaction #475961
tert-butyl (1-(cyanomethyl)piperidin-4-yl)methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Seite 1Weiter