benzoxazinone

Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #90224
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #90225
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc(Cl)cc(C(=O)NN)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #339081
3-bromo-N-[4-chloro-2-(hydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cc(Cl)cc(C(=O)NNC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #339126
3-bromo-N-[4-chloro-2-(N′-isopropylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
Rendimiento 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cc(Cl)cc(C(=O)N(C)N)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #339139
3-bromo-N-[4-chloro-2-(N-methylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CNN(C)C(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #339142
3-bromo-N-[4-chloro-2-(N,N′-dimethylhydrazinocarbonyl)-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
Rendimiento 134.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #562646
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #562647
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #603701
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #603702
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #658848
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #658849
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #687882
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #687883
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #729195
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #729196
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #729774
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #729775
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
Cc1cc(Cl)cc(C(=O)NC(C)C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #792169
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CNC(=O)c1cc(Cl)cc(C)c1NC(=O)c1cc(Br)nn1-c1ncccc1Cl
Reaction #792170
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
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