cycloheptyl-cyclobutylamine

O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #341067
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #341069
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #619193
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #619195
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #1207021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #1905558
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #1905560
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #2351002
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #2351004
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #2471425
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC2)s1
Reaction #2471427
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09