Impliqué dans 10 réactions

285829

CC(C)(C)c1cc(N)n(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #309040
desired product
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)c1cc(N)n(-c2ccc(C#N)cc2)n1
Reaction #309041
title compound
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cl
Reaction #309060
HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccncc3)cc2)n(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #309065
desired product
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)c1cc(N)n(-c2ccc(C#N)cc2)n1
Reaction #1227198
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC(C)(C)c1cc(N)n(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #1262012
desired product
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
CC(C)(C)c1cc(N)n(-c2ccc(C#N)cc2)n1
Reaction #1262013
title compound
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
Cl
Reaction #1262031
HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccncc3)cc2)n(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #1262036
desired product
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
CN(C)c1cc(C(C)(C)C)nn1-c1ccc([N+](=O)[O-])cc1
Reaction #1721275
1-(4′-nitrophenyl)-3-t-butyl-5-dimethylaminopyrazole
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01