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CC(=O)c1ccnc(Br)c1
Reaction #71052
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccnc(Br)c1
Reaction #71078
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(-c2cc(Br)ccn2)c1
Reaction #71530
4-bromo-2-(3′-bromophenyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(Br)cc(Br)c1OCc1ccccc1
Reaction #77706
15
Ausbeute 90.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(Br)ccc1O
Reaction #160103
6-bromo-2-methylpyridin-3-ol
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(Br)cc(Br)c1OCc1ccccc1
Reaction #179057
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(F)c(-c2nc(Br)c(F)c(Br)c2F)c1
Reaction #206012
DOI: 10.1039/C8SC04228D
NC(=O)c1cc(Br)c(O)c(Br)n1
Reaction #233643
DOI: 10.1039/C8SC04228D
COn1c(C(F)(F)F)nc2nc(Br)c(N)c(Br)c21
Reaction #251589
DOI: 10.1039/C8SC04228D
Fc1ccc(-c2nc(Br)cc(Br)c2CBr)c(F)c1
Reaction #273628
DOI: 10.1039/C8SC04228D
On1c(C(F)(F)F)nc2nc(Br)c(Cl)c(Br)c21
Reaction #287438
DOI: 10.1039/C8SC04228D
Cc1cc(Br)c(N)c(Br)n1
Reaction #314697
3-amino-2,4-dibromo-6-methylpyridine
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)c(NC(=O)CBr)c(Br)n1
Reaction #314698
N-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamide
Ausbeute 85.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)c(NC(=O)CN2CCN(CCO)CC2)c(Br)n1
Reaction #314699
N-[2,4-dibromo-6-methylpyridin-3-yl]-2-[4-(2-hydroxyethyl)piperazin-1-yl]acetamide
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCCC2)c(NC(=O)CN2CCN(CCO)CC2)c(N2CCCC2)n1
Reaction #314711
2-[4-(2-hydroxyethyl)piperazin-1-yl]-N-[2,4-bis(pyrrolidin-1-yl)-6-methyl-3-pyridyl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(Br)cc(Br)c1OCc1ccccc1
Reaction #364323
15
Ausbeute 90.6%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nc(Br)cc(Br)c2CBr)c(Cl)c1
Reaction #373259
DOI: 10.1039/C8SC04228D
Cc1c(Br)cc(Br)nc1-c1ccc(F)cc1F
Reaction #385536
DOI: 10.1039/C8SC04228D
O=C1CCc2c(cc(Br)nc2-c2ccccc2Cl)N1c1ccccc1Cl
Reaction #406736
DOI: 10.1039/C8SC04228D
Cc1cc(Br)c(N)c(Br)n1
Reaction #435737
3-amino-2,4-dibromo-6-methylpyridine
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
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