Recherche de Sous-structure

52

CCC(C)(C)c1ccc(S(=O)(=O)Nc2ncnc(OCCOc3ccc(Br)cn3)c2-c2ccc(C)cc2)cc1
Reaction #2367
4-tert-amyl-N-{6-[2-(5-bromopyridin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)COc4ncc(Br)cn4)cc3)ncnc2OCCOc2ncc(Br)cn2)cc1
Reaction #2395
4-[2-(5-bromopyrimidin-2-yloxy)-1,1-dimethylethyl]-N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
Rendement 33.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(N)ncnc2OCCOc2ncc(Br)cn2)cc1
Reaction #2402
6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-amine
Rendement 91.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N=S(C)(=O)c1ccc(Nc2ncc(Br)c(SC)n2)cc1
Reaction #66497
(RS)—N-(ethoxycarbonyl)-(4-{[4-{methylsulfanyl}-5-bromo-pyrimidin-2-yl]amino}phenyl)-S-methylsulfoximide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ncc(Br)cn1
Reaction #66498
sulfone
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #68818
solid
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(Nc2nc(Nc3ccc(C#N)cc3)ncc2Br)c(C)c1
Reaction #69646
4-[[5-bromo-4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile
Rendement 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC(O)COc1ccc(Nc2ncc(Br)c(Sc3ccccc3)n2)cc1
Reaction #78077
5-Bromo-2-{4-[2-hydroxy-3-(N,N-dimethylamino)propoxy]anilino}-4-(phenylthio)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(Br)c(=O)n12
Reaction #86515
product
Rendement 87.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3ccccc3)c(=O)n12
Reaction #86516
desired product
Rendement 44.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3cccc(F)c3)c(=O)n12
Reaction #86518
desired product
Rendement 33.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3cc(F)cc(F)c3)c(=O)n12
Reaction #86520
desired product
Rendement 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3ccccn3)c(=O)n12
Reaction #86522
desired product
Rendement 13.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(Br)c(=O)n12
Reaction #86526
7-(1-azidoethyl)-6-bromo-3-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one
Rendement 97.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3nccs3)c(=O)n12
Reaction #86535
desired product
Rendement 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3cscn3)c(=O)n12
Reaction #86537
desired product
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3ccc(F)cc3)c(=O)n12
Reaction #86539
desired product
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3cc(F)cc(F)c3)c(=O)n12
Reaction #86541
desired product
Rendement 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N=[N+]=[N-])c1nc2sccn2c(=O)c1Br
Reaction #86546
desired product
Rendement 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(N=[N+]=[N-])c1nc2sccn2c(=O)c1-c1cc(F)cc(F)c1
Reaction #86547
desired product
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
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