2-[4-[(5-bromo-4-ethyl-6-oxo-2-propylpyrimidin-1-yl)methyl]phenyl]benzonitrile

CCCc1nc(CC)c(-c2ccc(OC(C)C)cc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #174016
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1nc(CC)c(-c2ccc(OC(C)(C)CO[Si](C)(C)C(C)(C)C)cc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #176894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1nc(CC)c(-c2ccc(OC(F)(F)F)cc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #190703
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1nc(CC)c(Oc2cccc(CC)c2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #206561
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1nc(CC)c(-c2ccc(OCC3CC3)nc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #261310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1nc(CC)c(Oc2cc(C)ccn2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #272425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCc1nc(CC)c(-c2ccc(OC(C)C)c(F)c2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #389625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCc1nc(CC)c(-c2ccc(OCC)nc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #408339
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCc1nc(CC)c(-c2ccc(F)cc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #751558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCc1nc(CC)c(-c2ccc3c(c2)C(O)CC(C)(C)O3)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #758627
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCc1nc(CC)c(Oc2cccc3c2OC(C)(C)C3)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #775141
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCc1nc(CC)c(-c2ccc(OC(C)C)cc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #778285
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
C=Cc1c(CC)nc(CCC)n(Cc2ccc(-c3ccccc3C#N)cc2)c1=O
Reaction #888797
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCOc1ccc(-c2c(CC)nc(CCC)n(Cc3ccc(-c4ccccc4C#N)cc3)c2=O)cc1
Reaction #891914
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(CC)c(Oc2ccc(CC)cc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #915115
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(CC)c(-c2ccc(OC(C)C)cc2F)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #918225
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(CC)c(Oc2cccc(OC)c2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #1024001
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(CC)c(Oc2cc(F)ccc2F)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #1041633
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(CC)c(-c2ccc(OC(C)C)nc2)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #1048707
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(CC)c(-c2ccc3c(c2)CCO3)c(=O)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #1209698
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
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