Involved in 481 reactions

7286

Cc1cc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2C(Cl)Cl)n1
Reaction #4230
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=O)[n+]1c(-c2ccccn2)c(NC2CCCCC2)n2c(C)cc(C)nc21.[Cl-]
Reaction #7623
1-acetyl-3-cyclohexylamino-5,7-dimethyl-2-pyridin-2-yl-imidazo[1,2-a]pyrimidin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
[C-]#[N+]CCCCCCNc1c(-c2ccccn2)nc2nc(C)cc(C)n12
Reaction #51069
Compound ( 2 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(S(=O)(=O)CNc2nc(C)cc(C)n2)cc1
Reaction #63142
4,6-dimethyl-2-(4-tolylsulfonylmethylamino)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1cc(C)nc(NCSC(=S)N2CCOCC2)n1
Reaction #63143
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(=O)c1c(S(=O)(=O)NC(=O)Nc2nc(C)cc(C)n2)c2ccccc2n1C
Reaction #63271
desired product
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1.Cc1cc(C)n(N)c(=[NH2+])n1
Reaction #164526
1-Amino-4,6-dimethyl-1H-pyrimidin-2-ylidene-ammonium 2,4,6-Trimethyl-benzenesulfonate
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(C)nc(NC(=O)NS(=O)(=O)c2cccc3c2OC(C)(C)C3)n1
Reaction #206982
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2OS(=O)(=O)N(C)C)n1
Reaction #207655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)cc(C)n1
Reaction #242218
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(-c2nc3c(Cl)cc(Cl)cn3c2CNc2nc(C)cc(C)n2)cc1
Reaction #251496
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)[n+](N)c(N)n1
Reaction #297258
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1sccc1S(=O)(=O)NC(=O)Nc1nc(C)cc(C)n1
Reaction #343446
Methyl 3-[[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
Cc1cc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2C(Cl)Cl)n1
Reaction #366930
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
C[Se]c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)cc(C)n1
Reaction #367259
yellow solid
Yield 101.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
COC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)cc(C)n1
Reaction #367982
N-[(4,6-Dimethylpyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
Cc1cc(C)nc(NC(=O)NS(=O)(=O)c2cccc3c2CCCC3)n1
Reaction #380050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CSC(=Nc1nc(C)cc(C)n1)NS(=O)(=O)c1ccccc1-c1ccccc1
Reaction #408101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc(C)nc(N=S(C)C)n1
Reaction #451158
title compound
Yield 21.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
Cc1cc(C)nc(NC(=O)NS(=O)(=O)c2cc(Cl)sc2Cl)n1
Reaction #513626
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_10
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