3-(3-aminophenyl)-4-bromo-1-methylpyrazole

COc1ccccc1CC(=O)Nc1cccc(-c2nn(C)cc2Br)c1
Reaction #257993
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1ccc(-c2cccc(N)c2)n1
Reaction #318032
title compound
収率 72.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cn1cc(Br)c(-c2cccc(Nc3cc(C(F)(F)F)nc(-c4cccnc4)n3)c2)n1
Reaction #403877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc([N+](=O)[O-])cc3)c2)n1
Reaction #888481
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cn1ccc(-c2cccc(N)c2)n1
Reaction #909657
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc(OC(F)(F)F)cc3)c2)n1
Reaction #1305153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1ccc(OC(=O)Nc2cccc(-c3nn(C)cc3Br)c2)cc1
Reaction #1350570
title compound
収率 59.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)c3ccc(OC(F)(F)F)cc3)c2)n1
Reaction #1350571
title compound
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)NCc3ccc(OC(F)(F)F)cc3)c2)n1
Reaction #1350572
title compound
収率 202.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)c3ccc(Cl)cc3)c2)n1
Reaction #1350573
title compound
収率 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc(OC(F)(F)F)cc3)c2)n1
Reaction #1350574
title compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3cccc(F)c3)c2)n1
Reaction #1350575
title compound
収率 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
COc1cccc(CC(=O)Nc2cccc(-c3nn(C)cc3Br)c2)c1
Reaction #1350576
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccccc3F)c2)n1
Reaction #1350577
title compound
収率 32.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc([N+](=O)[O-])cc3)c2)n1
Reaction #1350578
title compound
収率 18.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
COc1ccccc1CC(=O)Nc1cccc(-c2nn(C)cc2Br)c1
Reaction #1350579
title compound
収率 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
Cn1cc(Br)c(-c2cccc(NC(=O)c3ccc(OC(F)(F)F)cc3)c2)n1
Reaction #1848481
title compound
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_01
Cn1cc(Br)c(-c2cccc(NC(=O)c3cccs3)c2)n1
Reaction #1848482
title compound
収率 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_01
Cn1cc(Br)c(-c2cccc(NC(=O)c3ccc(Cl)cc3)c2)n1
Reaction #1848483
title compound
収率 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_01
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc(OC(F)(F)F)cc3)c2)n1
Reaction #1848484
title compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_01
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