4-chloro-2-methylthiopyrimidine

CSc1nccc(Oc2cccc(C(F)(F)F)c2)n1
Reaction #896
phenoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1nccc(OCC(F)(F)F)n1
Reaction #1012
2-methylthio-4-(2,2,2-trifluoroethoxy)pyrimidine
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1nccc(F)n1
Reaction #9856
4-fluoro-2-methylthiopyrimidine
Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CSc1nccc(N)n1
Reaction #44525
2-(methylsulfanyl)-4-pyrimidinamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSc1nccc(OCc2ccccc2)n1
Reaction #47944
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSc1nccc(NN)n1
Reaction #70245
N-(2-methylsulfanyl-pyrimidin-4-yl)-hydrazine
Ausbeute 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(Cn2cc(-c3ccnc(SC)n3)c(-c3cccc([N+](=O)[O-])c3)n2)cc1
Reaction #74160
title compound
Ausbeute 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CSc1nccc(N2CCn3c2cc(-c2ccccc2)cc3=O)n1
Reaction #173303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1nccc(Oc2ccccc2)n1
Reaction #216584
2-methylthio-4-phenoxypyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CS(=O)(=O)c1nccc(Cl)n1
Reaction #216585
4-chloro-2-methanesulphonylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CSc1nccc(-n2cnc3ccc(N)cc32)n1
Reaction #222068
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(I)n1
Reaction #225896
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(OCC(F)(F)F)n1
Reaction #237016
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(N2CCc3ccccc32)n1
Reaction #244176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(-c2cn[nH]c2)n1
Reaction #250295
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(C(C#N)C(=O)OC(C)(C)C)n1
Reaction #252377
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(NCC2CCN(C(=O)OCc3ccc(C)cc3)CC2)n1
Reaction #258850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCOc1ccnc(SC)n1
Reaction #259898
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1nccc(F)n1
Reaction #265082
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CSc1nccc(-c2ccc3c(c2)ncn3-c2ccnc(NC(C)c3ccccc3)n2)n1
Reaction #286570
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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