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CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1

4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine

Rendimiento 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

Cc1cc(NCCC(=O)Nc2ccc3nc(C)cc(N)c3c2)nc(N)n1

Reaction #47790

Rendimiento 36.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

Cc1cc(NCc2ccc(NC(=O)c3ccc4nc(C)cc(N)c4c3)cc2)nc(N)n1

Reaction #47793

Rendimiento 82.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1

Reaction #81893

4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine

Rendimiento 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04

Cc1cc(N)nc(N)n1

Reaction #82525

2,4-diamino-6-methylpyrimidine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04

CCCNc1cc(C)nc(N)n1

Reaction #82560

2-amino-4-propylamino-6-methylpyrimidine

Rendimiento 105.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04

Cc1cc(Cl)nc(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)n1

Reaction #157129

4-chloro-N,N-di-BOC-6-methylpyrimidin-2-amine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

CC(=O)c1ccc(Nc2cc(C)nc(N)n2)cc1

Reaction #175996

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Cc1cc(Nc2ccccc2)nc(N)n1

Reaction #177883

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CSc1cc(C)nc(N)n1

Reaction #188636

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CC(=O)Nc1nc2ccc(-c3cc(C)nc(N)n3)cc2s1

Reaction #206103

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CC(=O)c1cccc(Nc2cc(C)nc(N)n2)c1

Reaction #207593

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Cc1cc(Cl)nc(NCc2c(-c3ccc(C#N)cc3)nc3ccc(Cl)cn23)n1

Reaction #230705

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction #231452

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Cc1cc(N(C)C)nc(N)n1

Reaction #278516

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

Cc1cc(N)nc(N)n1

Reaction #279284

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

CCOC(=O)C1CCN(c2cc(C)nc(N)n2)CC1

Reaction #289884

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

Cc1nc(N)nc(Cl)c1I

Reaction #330332

Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02

Cc1cc(Nc2cccc([N+](=O)[O-])c2)nc(N)n1

Reaction #386393

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)

Cc1ccc2nc(-c3ccc(F)cc3)c(CNc3nc(C)cc(Cl)n3)n2c1

Reaction #394588

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)

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