1,5-dimethyl-3-oxo-2-phenylpyrazole-4-carboxylic acid

COC(=O)c1c(C)n(C)n(-c2ccccc2)c1=O
Reaction #503065
methyl 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylate
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CC1(C)S[C@@H]2CC(=O)N2[C@H]1C(=O)O
Reaction #572860
penicillanic acid
Ausbeute 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
Cc1c(C(=O)Nc2ccc(O)cc2)c(=O)n(-c2ccccc2)n1C
Reaction #607844
title compound
Ausbeute 52.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3Cl)c(F)c2)c(=O)n(-c2ccccc2)n1C
Reaction #607848
title compound
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3)c(F)c2F)c(=O)n(-c2ccccc2)n1C
Reaction #607851
title compound
Ausbeute 33.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2cc(F)c(Oc3ccnc(C(N)=O)c3)cc2F)c(=O)n(-c2ccccc2)n1C
Reaction #607855
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3)cc2Cl)c(=O)n(-c2ccccc2)n1C
Reaction #607858
title compound
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3)cn2)c(=O)n(-c2ccccc2)n1C
Reaction #607860
title compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(O)cn2)c(=O)n(-c2ccccc2)n1C
Reaction #607863
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(O)c(F)c2)c(=O)n(-c2ccccc2)n1C
Reaction #607864
title compound
Ausbeute 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2cc(F)c(O)cc2Cl)c(=O)n(-c2ccccc2)n1C
Reaction #607871
title compound
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(O)c(Cl)c2)c(=O)n(-c2ccccc2)n1C
Reaction #607873
title product
Ausbeute 72.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(O)cc2F)c(=O)n(-c2ccccc2)n1C
Reaction #607876
title compound
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(N)c3)cc2)c(=O)n(-c2ccccc2)n1C
Reaction #607880
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(O)cn2)c(=O)n(C)n1-c1ccccc1
Reaction #607883
title compound
Ausbeute 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(O)cc2)c(=O)n(-c2ccccc2)n1C
Reaction #607902
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1c(C(=O)Nc2ccc(Oc3ccnc(N)c3)cc2)c(=O)n(-c2ccccc2)n1C
Reaction #957594
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Cc1c(C(=O)Nc2ccc(Oc3ccnc(N)c3Cl)cc2)c(=O)n(-c2ccccc2)n1C
Reaction #957595
title compound
Ausbeute 52.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3Cl)c(F)c2)c(=O)n(-c2ccccc2)n1C
Reaction #957598
title compound
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Cc1c(C(=O)Nc2ccc(Oc3ccnc(C(N)=O)c3)c(F)c2F)c(=O)n(-c2ccccc2)n1C
Reaction #957603
title compound
Ausbeute 33.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
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