4-Piperidinecarboxamide

COc1cccc(N2CCC(C(N)=O)CC2)c1
Reaction #393
Выход 0.0%750 AstraZeneca ELN dataset
O=C(NCc1ccccc1)C1CCNCC1
Reaction #1171
N-benzyl-4-piperidinecarboxamide
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C1CCN(Cc2ccc3c(c2)cc(-c2ccc(Cl)c4c2C(=O)NC4)n3C(=O)OC(C)(C)C)CC1
Reaction #49305
4-chloro-7-[1-(tert-butoxycarbonyl)-5-(4-methoxycarbonylpiperidinomethyl)indol-2-yl]isoindolinone
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NC(=O)C1CCN(CCOc2ccccc2CCc2ccccc2)CC1
Reaction #55336
2-[2-(4-carbamoylpiperidino)ethoxy]bibenzyl
Выход 82.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(Nc1ncnc2cc(C(=O)N3CCC(C(N)=O)CC3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62488
6-chloro-4-[1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-(4-aminocarbonyl-piperidin-1-yl-carbonyl)-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NC(=O)C1CCN(Cc2ccccc2)CC1
Reaction #75607
1-benzyl-4-piperidine carboxamide
Выход 49.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)N1CCN(c2ccc(-c3noc(-c4ccc(CN5CCC(C(N)=O)CC5)cc4)n3)cn2)CC1.Cl.Cl
Reaction #168084
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)C1CCN(Cc2ccccc2)CC1
Reaction #185319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)C1CCN(CCOc2ccccc2CCc2ccccc2)CC1
Reaction #185656
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)C1CCN(CCCCl)CC1
Reaction #196460
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)C1CCN(c2nc(Cl)nc3[nH]ccc23)CC1
Reaction #209347
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N=C(c1cccc(NC(=O)Nc2ccc(S(=O)(=O)NCc3ccc(S(N)(=O)=O)cc3)cc2)c1)N1CCC(C(N)=O)CC1
Reaction #235149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NC(CC(=O)N1CCn2c(C(F)(F)F)nc(C(=O)N3CCC(C(N)=O)CC3)c2C1)Cc1cc(F)c(F)cc1F
Reaction #236299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)C1CCN(c2ccc(-c3c4cccc(C(F)(F)F)c4nn3Cc3ccccc3)cc2)CC1
Reaction #257505
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1Sc1ccc(-c2ccnc(N3CCC(C(N)=O)CC3)c2)cc1C(F)(F)F
Reaction #258465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)C1CCN(c2cc(-c3ccc(F)cc3)nc3ccsc23)CC1
Reaction #268979
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc2nc(-c3ccc(F)cc3)cc(N3CCC(C(N)=O)CC3)c2c1
Reaction #271465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)C1CCN(C2CN(C(c3ccccc3)c3ccccc3)C2)CC1
Reaction #295106
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)C1CCN(C(=O)c2ccccc2-c2ccc(C(F)(F)F)cc2)CC1
Reaction #297769
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N[C@@H](CC(=O)N1CCn2c(C(F)(F)F)nc(C(=O)N3CCC(C(N)=O)CC3)c2C1)Cc1cc(F)c(F)cc1F
Reaction #308623
(R)-[3-[1-(4-carbamoyl-piperidine-1-carbonyl)-3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazin-7-yl]-3-oxo-1-(2,4,5-trifluoro-benzyl)-propyl]-carbamic acid tert-butyl ester
Выход 100.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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