Ähnlichkeitssuche

197896

N#Cc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163045
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163046
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163047
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163048
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163049
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(F)c(NC(CO)c2ccc(F)cc2)c(F)c1Nc1cc(C2CC2)[nH]n1
Reaction #203482
DOI: 10.1039/C8SC04228D
Cc1nc(NC(CO)c2ccc(F)cc2)nc(Nc2cc(C3CC3)[nH]n2)c1N
Reaction #204373
DOI: 10.1039/C8SC04228D
N#Cc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1NC(CO)c1ccc(F)cc1
Reaction #231491
DOI: 10.1039/C8SC04228D
NCc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1NC(CO)c1ccc(F)cc1
Reaction #280667
DOI: 10.1039/C8SC04228D
Cc1nc(NC(CO)c2ccc(F)cc2)nc(Nc2cc(C3CC3)[nH]n2)c1[N+](=O)[O-]
Reaction #376831
DOI: 10.1039/C8SC04228D
Cc1nc(N[C@@H](CO)c2ccc(F)cc2)nc2c1ncn2-c1cc(C2CC2)[nH]n1
Reaction #1179379
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1ncc2nnn(-c3cc(C4CC4)[nH]n3)c2n1)c1ccc(F)cc1
Reaction #1179380
title compound
Ausbeute 41.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N[C@@H](C)c2ccc(F)cc2)nc2c1ncn2-c1cc(C2CC2)[nH]n1
Reaction #1179381
title compound
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H](Nc1cc2c(cn1)ncn2-c1cc(C2CC2)[nH]n1)c1ccc(F)cc1
Reaction #1179389
title compound
Ausbeute 153.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1179395
solid
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N[C@@H](CO)c2ccc(F)cc2)nc(Nc2cc(C3CC3)[nH]n2)c1[N+](=O)[O-]
Reaction #1179397
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1ncc(N)c(Nc2cc(C3CC3)[nH]n2)n1)c1ccc(F)cc1
Reaction #1179398
title compound
Ausbeute 5.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N[C@@H](CO)c2ccc(F)cc2)nc(Nc2cc(C3CC3)[nH]n2)c1N
Reaction #1179406
(R)-2-[5-Amino-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)-6-methylpyrimidin-2-ylamino]-2-(4-fluorophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N[C@@H](C)c2ccc(F)cc2)nc(Nc2cc(C3CC3)[nH]n2)c1N
Reaction #1179407
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cnc(N[C@@H](CO)c2ccc(F)cc2)cc1Nc1cc(C2CC2)[nH]n1
Reaction #1179425
(R)-2-(5-Amino-4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyridin-2-ylamino)-2-(4-fluorophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
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