cyanobenzoxazinone

CNC(=O)c1cc(C#N)cc(C)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #341608
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cc(C#N)cc(C(N)=O)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #341609
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CNC(=O)c1cc(C#N)cc(C)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #531823
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1cc(C#N)cc(C(N)=O)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #531824
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CNC(=O)c1cc(C#N)cc(C)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #1383719
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
Cc1cc(C#N)cc(C(N)=O)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #1383720
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
CNC(=O)c1cc(C#N)cc(C)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #1838942
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Cc1cc(C#N)cc(C(N)=O)c1NC(=O)c1cc(Cl)nn1-c1ncccc1Cl
Reaction #1838943
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10