2-piperidin-1-ylethanamine

CCOC(=O)c1cn(-c2ccc3c(c2)CCC3)c2nc(NCCN3CCCCC3)ncc2c1=O
Reaction #40612
8-indan-5-yl-5-oxo-2-(2-piperidin-1-yl-ethylamino)-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #40640
solid
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(-c2csc3c(/C=C/C(=O)NCCN4CCCCC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45423
desired product
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NCCN1CCCCC1)c1sc2c(ccc(=O)n2-c2ccccc2)c1Nc1ccccc1
Reaction #58703
title compound
Ausbeute 21.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)N1CCN(C(=O)c2ccc(NCCN3CCCCC3)nc2)CC1
Reaction #58743
title compound
Ausbeute 37.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(NCCN1CCCCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67817
3-[(2-fluoro-4-iodophenyl)amino]-N-(2-piperidin-1-ylethyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1ccc(NCCN2CCCCC2)c(F)c1
Reaction #84465
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc2[nH]c(=O)c3cnn(C4CCOCC4)c3c2cc1C(=O)NCCN1CCCCC1
Reaction #156313
7-methyl-4-oxo-N-[2-(piperidin-1-yl)ethyl]-1-(tetrahydro-2H-pyran-4-yl)-4,5-dihydro-1H-pyrazolo[4,3-c]quinoline-8-carboxamide
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cc(-c2nc3ccccc3o2)ccc1NCCN1CCCCC1
Reaction #161492
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NCCN1CCCCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #165982
3-[(2-fluoro-4-iodophenyl)amino]-N-(2-piperidin-1-ylethyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
[N-]=[N+]=Nc1ccc(C(=O)NCCN2CCCCC2)cc1
Reaction #174325
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2CCOCC2)c2sc(NC(=O)c3ccnc(NCCN4CCCCC4)c3)nc12
Reaction #176066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[O-][n+]1nc(NCCN2CCCCC2)nc2ccc3c(c21)CCC3
Reaction #178447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)NCCN1CCCCC1
Reaction #179199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(Cc1ccc(Cl)c(Cl)c1)C(=O)C1=C(O)C(=O)N(CCN2CCCCC2)C1
Reaction #192085
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(COc2ccccc2-c2cc(-c3cccc(C(=O)OCCN4CCCCC4)c3)c(C#N)c(N)n2)cc1
Reaction #197333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(Oc2ccnc3cc(OC)c(OC)cc23)ccc1NC(=O)NCCN1CCCCC1
Reaction #201478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)Cn1ncc2cc(Oc3ccc(F)cc3)c(C(=O)NCCN3CCCCC3)cc21
Reaction #206138
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl.O=C(NCCN1CCCCC1)c1cc(Cl)cc2c1OCCO2
Reaction #214604
N-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochloride
Ausbeute 129.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COC(=O)C[C@@H]1Cc2cc(Cl)c3[nH]nc(Cl)c3c2CN(CCN2CCCCC2)C1=O
Reaction #219646
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
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