Involved in 8 reactions

795758

CCOC(=O)Cc1cc(Cl)c(NC(=O)c2cn(C)c3ccc(F)cc23)cc1F
Reaction #271723
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1cc(C(=O)N2CCN(c3ccc(OCCCN4CCCCC4)cc3)CC2)c2cc(F)ccc21
Reaction #778593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cn1cc(C(=O)O)c2cc(F)ccc21
Reaction #1044311
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC1CCCCN1CCCOc1ccc(N2CCN(C(=O)c3cn(C)c4ccc(F)cc34)CC2)cc1
Reaction #1213012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cn1cc(C(=O)O)c2cc(F)ccc21
Reaction #1459888
5-fluoro-1-methylindole-3-carboxylic acid
Yield 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
CCOC(=O)Cc1cc(Cl)c(NC(=O)c2cn(C)c3ccc(F)cc23)cc1F
Reaction #1459889
ethyl (5-chloro-2-fluoro-4-(((5-fluoro-1-methyl-3-indolyl)carbonyl)amino)phenyl)acetate
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
Cn1cc(C(=O)N2CCN(c3ccc(OCCCN4CCCCC4)cc3)CC2)c2cc(F)ccc21
Reaction #1521767
title compound
Yield 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
CC1CCCCN1CCCOc1ccc(N2CCN(C(=O)c3cn(C)c4ccc(F)cc34)CC2)cc1
Reaction #1521772
title compound
Yield 45.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11