phenyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate

COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)NC1=NC(OC)=CN(C)N1
Reaction #925
oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1nc(C)nc(NC(=O)NS(=O)(=O)C2=CCCC=C2c2nn(C)c(=O)o2)n1
Reaction #63154
subject compound
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CON=C(Cl)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #191461
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccn3c2C(=O)OCC3)n1
Reaction #196038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #203725
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2Cc2nnc(SC)s2)n1
Reaction #319159
subject compound
Ausbeute 32.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CN=S(=O)(NC(=O)Nc1nc(C)nc(OC)n1)c1ccccc1Cl
Reaction #334184
white solid
Ausbeute 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
COc1nc(C)nc(NC(=O)NS(=O)(=O)Cc2ccccc2-c2nnc(SC)o2)n1
Reaction #343003
subject compound
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
COc1nc(C)nc(NC(=O)NS(=O)(=O)C2=CCCC=C2c2nn(C)c(=O)o2)n1
Reaction #343008
subject compound
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-n2nnnc2C)n1
Reaction #788265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CN=S(=O)(NC(=O)Nc1nc(C)nc(OC)n1)c1ccccc1Cl
Reaction #1066146
white solid
Ausbeute 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
CON=C(Cl)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1069480
subject compound
Ausbeute 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_02
COC(=O)c1ccn(C)c1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1168430
title compound
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
CON=C(Cl)c1ccccc1S(=O)(=O)NC(=O)Nc1nc(C)nc(OC)n1
Reaction #1251909
subject compound
Ausbeute 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_03
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-n2nnnc2C)n1
Reaction #1340043
desired product
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_05
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccn3c2C(=O)OCC3)n1
Reaction #1795112
title compound
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_10
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2sccc2C2OCCO2)n1
Reaction #1810490
product
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_08
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-n2nnnc2C)n1
Reaction #2138287
desired product
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_05
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-n2nnnc2C)n1
Reaction #2159781
desired product
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_04
COc1nc(C)nc(NC(=O)NS(=O)(=O)c2ccccc2-n2nnnc2C)n1
Reaction #2319221
desired product
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_11
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