azepan-1-amine

O=C(NN1CCCCCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67825
N-azepan-1-yl-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NN1CCCCCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #165990
N-azepan-1-yl-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1c2cccnc2N(N2CCCCCC2)C2=NCCN12
Reaction #270472
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2ccccc2N(N2CCCCCC2)C2=NCCN12
Reaction #285196
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NN1CCCCCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #306096
N-azepan-1-yl-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(NN1CCCCCC1)C1=NN(c2ccc(Cl)cc2Cl)C(c2ccc(Br)cc2)C1
Reaction #308391
5-(4-Bromo-phenyl)-1-(2,4-dichloro-phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylic acid azepan-1-ylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc2ncnc(Oc3ccc(NC(=O)NN4CCCCCC4)cc3)c2cc1OC
Reaction #405979
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(Nc2nc(Cl)nc(NN3CCCCCC3)n2)cc1Cl
Reaction #433876
solid 152
المردود 31.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CSc1c(C(=O)NN2CCCCCC2)nn(-c2ccc(Cl)cc2Cl)c1-c1ccc(Cl)cc1
Reaction #594610
Compound 3
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=C(NN1CCCCCC1)C1=NN(c2ccc(Cl)cc2Cl)C(c2ccc(Br)cc2)C1
Reaction #684985
5-(4-Bromo-phenyl)-1-(2,4-dichloro-phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylic acid azepan-1-ylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CC(C)c1cc(-c2ccc(F)cc2)c(-c2ccccc2)n1C1CCCCCN1
Reaction #791931
3-(4-Fluorophenyl)-1-hexahydroazepinyl-5-isopropyl-2-phenyl-pyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_01
COc1ccc(Nc2nc(Cl)nc(NN3CCCCCC3)n2)cc1Cl
Reaction #806595
solid 152
المردود 31.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COc1cc(Oc2ccnc3cc(OC)c(OC)cc23)ccc1NC(=O)NN1CCCCCC1
Reaction #808689
title compound
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COc1cc2ncnc(Oc3ccc(NC(=O)NN4CCCCCC4)cc3)c2cc1OC
Reaction #808690
title compound
المردود 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COc1cc2nccc(Oc3ccc(NC(=O)NN4CCCCCC4)cc3)c2cc1OC
Reaction #808692
title compound
المردود 47.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COc1cc2nccc(Oc3ccc(NC(=O)NN4CCCCCC4)c(F)c3)c2cc1OC
Reaction #808693
title compound
المردود 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COc1ccc(Nc2nc(Cl)nc(NN3CCCCCC3)n2)cc1Cl
Reaction #1002313
solid 152
المردود 31.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COc1ccc(Nc2nc(Cl)nc(NN3CCCCCC3)n2)cc1Cl
Reaction #1003286
solid 152
المردود 31.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COc1cc2nccc(Oc3ccc(NC(=O)NN4CCCCCC4)c(F)c3)c2cc1OC
Reaction #1043041
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COc1cc2nccc(Oc3ccc(NC(=O)NN4CCCCCC4)cc3)c2cc1OC
Reaction #1048964
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
الصفحة 1التالي