2-amino-4,6-dimethoxypyrimidine

COc1cc(OC)nc(NC(=O)CC(F)=C(F)F)n1
Reaction #1042
title compound
Rendement 10.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ccccc2CCl)n1
Reaction #4233
white solid
Rendement 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1cc(OC)nc(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)n1
Reaction #64666
desired product
Rendement 103.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOc1ccccc1OS(=O)(=O)NC(=O)Nc1nc(OC)cc(OC)n1
Reaction #64667
desired product
Rendement 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2c(Cl)nc3ccccn23)n1
Reaction #175023
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)n1
Reaction #177903
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)nc(NC(=O)CC(F)=C(F)F)n1
Reaction #195555
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)Nc2ccccc2C(O)C2CC2)n1
Reaction #215714
title product
Rendement 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ccccc2-c2ccno2)n1
Reaction #222125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ccccc2OS(=O)(=O)N(C)C)n1
Reaction #226790
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCOC(=O)c1ccccc1OS(=O)(=O)NC(=O)Nc1nc(OC)cc(OC)n1
Reaction #226813
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)Nc1nc(OC)cc(OC)n1
Reaction #257824
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2cc(C(F)(F)F)ccc2S(=O)(=O)N(C)C)n1
Reaction #264337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2cscc2C)n1
Reaction #269435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)Oc2ccccc2-c2nnco2)n1
Reaction #281558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2c(C(=O)C3CC3)cnn2C)n1
Reaction #318587
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2cscc2C)n1
Reaction #323710
desired product
Rendement 43.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COC(=O)c1ccc(-c2ccccc2S(=O)(=O)NC(=O)Nc2nc(OC)cc(OC)n2)o1
Reaction #342998
title compound
Rendement 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ccccc2CCOC(C)=O)n1
Reaction #343017
2-[2-(acetyloxy)ethyl]-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]benzenesulfonamide
Rendement 54.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
COC(=O)c1sccc1S(=O)(=O)NC(=O)Nc1nc(OC)cc(OC)n1
Reaction #343447
Methyl 3 [[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl] aminosulfonyl]-2-thiophenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
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