5-phenyl-3-piperidin-4-yl-1H-indole-7-carboxamide

NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CCCCl)CC3)c[nH]c12
Reaction #783941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CCN4C(=O)c5ccccc5C4=O)CC3)c[nH]c12
Reaction #1626565
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CCCl)CC3)c[nH]c12
Reaction #1660727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
Cn1cnc(S(=O)(=O)N2CCC(c3c[nH]c4c(C(N)=O)cc(-c5ccccc5)cc34)CC2)c1
Reaction #2237171
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CCCCl)CC3)c[nH]c12
Reaction #2354667
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CCN4C(=O)c5ccccc5C4=O)CC3)c[nH]c12
Reaction #2354672
crude product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CCCl)CC3)c[nH]c12
Reaction #2354673
desired product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
C=CS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4ccccc4)cc23)CC1
Reaction #2354678
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
Cn1cnc(S(=O)(=O)N2CCC(c3c[nH]c4c(C(N)=O)cc(-c5ccccc5)cc34)CC2)c1
Reaction #2354759
title compound
Ausbeute 40.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)c4cccs4)CC3)c[nH]c12
Reaction #2354760
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)c4csc(-c5ccon5)c4)CC3)c[nH]c12
Reaction #2354761
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)c4ccc(CNCc5ccccc5)s4)CC3)c[nH]c12
Reaction #2354762
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
CC(=O)Nc1nc(C)c(S(=O)(=O)N2CCC(c3c[nH]c4c(C(N)=O)cc(-c5ccccc5)cc34)CC2)s1
Reaction #2354763
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
Cc1nn(C)c(Cl)c1S(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4ccccc4)cc23)CC1
Reaction #2354764
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
Cc1nc(C)c(S(=O)(=O)N2CCC(c3c[nH]c4c(C(N)=O)cc(-c5ccccc5)cc34)CC2)s1
Reaction #2354769
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
Cc1ncc(S(=O)(=O)N2CCC(c3c[nH]c4c(C(N)=O)cc(-c5ccccc5)cc34)CC2)n1C
Reaction #2354770
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)c4ccsc4)CC3)c[nH]c12
Reaction #2354776
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)c4ccsc4)CC3)c[nH]c12
Reaction #2397183
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)