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547588

CC(Nc1nc(Nc2cnccn2)cc(OCC2CCCO2)n1)c1ccc(F)cc1
Reaction #185331
DOI: 10.1039/C8SC04228D
CC(Nc1nc(Nc2cnccn2)cc(-c2cnc([Si](C(C)C)(C(C)C)C(C)C)o2)n1)c1ccc(F)cc1
Reaction #240262
DOI: 10.1039/C8SC04228D
CC(Nc1nc(Nc2cnccn2)cc(-c2ccc(S(C)(=O)=O)cc2)n1)c1ccc(F)cc1
Reaction #269518
DOI: 10.1039/C8SC04228D
CC(Nc1nc(Cl)cc(Nc2cnccn2)n1)c1ccc(F)cc1
Reaction #372835
DOI: 10.1039/C8SC04228D
CC(Nc1nc(Nc2cnccn2)cc(N2CCNC2=O)n1)c1ccc(F)cc1
Reaction #911656
DOI: 10.1039/C8SC04228D
C[C@H](Nc1nc(Cl)cc(Nc2cnccn2)n1)c1ccc(F)cc1
Reaction #1274860
objective compound
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(-c2ccc(S(C)(=O)=O)cc2)n1)c1ccc(F)cc1
Reaction #1274861
(S)—N2-[1-(4-fluorophenyl)ethyl]-6-[4-(methylsulfonyl)phenyl]-N4-(pyrazin-2-yl)pyrimidine-2,4-diamine
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(N2CCNC2=O)n1)c1ccc(F)cc1
Reaction #1274867
(S)-1-{2-[1-(4-fluorophenyl)ethylamino]-6-(pyrazin-2-ylamino)pyrimidin-4-yl}imidazolidin-2-one
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](c1ncc(-c2cc(Nc3cnccn3)nc(N[C@@H](C)c3ccc(F)cc3)n2)o1)(C(C)C)C(C)C
Reaction #1274868
(S)—N2-[1-(4-fluorophenyl)ethyl]-N4-(pyrazin-2-yl)-6-[2-(triisopropylsilyl)oxazol-5-yl]pyrimidine-2,4-diamine
Ausbeute 65.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CN(c2cc(Nc3cnccn3)nc(N[C@@H](C)c3ccc(F)cc3)n2)C1
Reaction #1274882
objective compound
Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(OCC2CCCO2)n1)c1ccc(F)cc1
Reaction #1274898
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(-c2cnccc2C(N)=O)n1)c1ccc(F)cc1
Reaction #1274899
(S)-3-{2-[1-(4-fluorophenyl)ethylamino]-6-(pyrazin-2-ylamino)pyrimidin-4-yl}isonicotinamide
Ausbeute 16.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(C#N)cc(Nc2cnccn2)n1)c1ccc(F)cc1
Reaction #1274918
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(N2CC(C#N)C2)n1)c1ccc(F)cc1
Reaction #1274923
objective compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Cl)cc(Nc2cnccn2)n1)c1ccc(F)cc1
Reaction #2130581
objective compound
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(-c2ccc(S(C)(=O)=O)cc2)n1)c1ccc(F)cc1
Reaction #2130582
(S)—N2-[1-(4-fluorophenyl)ethyl]-6-[4-(methylsulfonyl)phenyl]-N4-(pyrazin-2-yl)pyrimidine-2,4-diamine
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(N2CCNC2=O)n1)c1ccc(F)cc1
Reaction #2130589
(S)-1-{2-[1-(4-fluorophenyl)ethylamino]-6-(pyrazin-2-ylamino) pyrimidin-4-yl}imidazolidin-2-one
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](c1ncc(-c2cc(Nc3cnccn3)nc(N[C@@H](C)c3ccc(F)cc3)n2)o1)(C(C)C)C(C)C
Reaction #2130590
(S)—N2-[1-(4-fluorophenyl)ethyl]-N4-(pyrazin-2-yl)-6-[2-(tri isopropylsilyl) oxazol-5-yl]pyrimidine-2,4-diamine
Ausbeute 65.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CN(c2cc(Nc3cnccn3)nc(N[C@@H](C)c3ccc(F)cc3)n2)C1
Reaction #2130604
objective compound
Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cnccn2)cc(OCC2CCCO2)n1)c1ccc(F)cc1
Reaction #2130621
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
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