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168

Cc1ncc([N+](=O)[O-])cc1Nc1nccc(-c2cccnc2)n1
Reaction #732
Ausbeute 18.9%
Cc1ncc([N+](=O)[O-])cc1Nc1nccc(-c2cccnc2)n1
Reaction #733
Ausbeute 21.2%
Clc1cccc(Nc2nccc(-c3ccnc(Cl)c3)n2)c1
Reaction #2253
N-(3-chloro-phenyl)-4-(2-chloro4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc(-c2ccnc(Nc3cccc(Cl)c3)n2)cc1
Reaction #2254
N-(3-chloro-phenyl)-4-(N-oxido4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(-c2ccco2)c2cnn(Cc3ccccc3F)c2n1
Reaction #8388
title compound
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
OCCNc1nc(-c2ccco2)c2cnn(CCc3ccccc3)c2n1
Reaction #8398
title compound
Ausbeute 57.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(-c2ccco2)c2ccn(Cc3ccccc3F)c2n1
Reaction #11850
title compound
Ausbeute 51.4%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N(CCCN)Cc1cccc(-c2ccnc(NCc3ccc(O)cc3)n2)c1
Reaction #42987
N-(3-Amino-propyl)-N-{3-[2-(4-hydroxy-benzylamino)-pyrimidin-4-yl]-benzyl}-methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
NCCCNC(=O)c1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43038
N-(3-Amino-propyl)-3-{2-[2-(4-hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43090
4-{2-[4-(3-Butoxy-phenyl)-pyrimidin-2-ylamino]-ethyl}-phenol
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CCNc2nccc(-c3cccc(CNc4cnccn4)c3)n2)cc1
Reaction #43115
4-(2-{4-[3-(Pyrazin-2-ylaminomethyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43119
4-(2-{4-[3-(Isopropylamino-methyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NCc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43189
product
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NCc1cccc(-c2ccnc(NCCc3ccc(O)c(Cl)c3)n2)c1
Reaction #43190
product
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(C#N)(NC(=O)C(CC2CCCCC2)Nc2nccc(C#N)n2)CC1
Reaction #53533
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(-c2ccnc(Nc3ccccc3)n2)cnc1C=NO
Reaction #60621
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON=Cc1ncc(-c2ccnc(Nc3ccccc3)n2)n1C(C)C
Reaction #60622
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1cncc1C(=O)C=CN(C)C
Reaction #60627
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(NCc2ccccc2)nc1-c1c[nH]c2ncc(C(F)(F)F)cc12
Reaction #69112
2-(benzylamino)-4-(5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(-c2nc3[nH]ncc3cc2-c2ccnc(NCC3CC3)n2)c1
Reaction #70887
desired compound
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
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