pyrimidine

O=C(NCc1ccc2c(c1)OCO2)c1ccc2ccn(-c3ccnc(-n4ccnc4)n3)c2c1
Reaction #51465
N-[(1,3-benzodioxol-5-yl)methyl]-1-[2-(1H-imidazol-1-yl)pyrimidin-4-yl]indole-6-carboxamide
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #60141
primary amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #60145
primary amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #65124
( IV )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCOC1
Reaction #79800
4-amino-5-(4-phenoxyphenyl)-7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]pyrimidine
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COCC(C)(C)Nc1nc(Cl)ncc1Br
Reaction #169462
title compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1nc(C(=O)O)c(OCc2ccccc2)c(=O)n1C
Reaction #191266
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(COc2cnc(N3CCNCC3)nc2)cc1
Reaction #243067
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(Nc2ncnc(Nc3ccc(S(C)(=O)=O)cc3)c2[N+](=O)[O-])CC1
Reaction #252289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc(N)nc(N)c1N=Nc1ccc(Br)cc1
Reaction #285611
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1csc(-c2cncnc2)c1
Reaction #288234
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CCC(NC(=O)c1ccc(NCCCc2c(NC(C)=O)nc(NC(C)=O)[nH]c2=O)cc1)C(=O)OC
Reaction #296182
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
—
Reaction #362429
( 35 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCOC(=O)C(=O)c1cnc(C(C)(C)C)nc1
Reaction #381205
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc2c(Cl)nc(-c3cccnc3)nc2s1
Reaction #387619
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=P(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #398432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1nc(Cl)nc(Cl)c1OC
Reaction #420104
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(Nc1nc(-c2ccco2)c(C(=O)c2ccncn2)s1)c1ccncc1
Reaction #424652
Compound 375
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(NCc1ccc2c(c1)OCO2)c1ccc2ccn(-c3ccnc(-n4ccnc4)n3)c2c1
Reaction #439801
N-[(1,3-benzodioxol-5-yl)methyl]-1-[2-(1H-imidazol-1-yl)pyrimidin-4-yl]indole-6-carboxamide
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
COc1nc(C)nc(Cl)c1Cl
Reaction #460631
4,5-Dichloro-6-methoxy-2-methylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
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