Recherche de Sous-structure

1176964

N#Cc1cnc(N)cc1N
Reaction #3511
2,4-diamino-5-cyanopyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc([N+](=O)[O-])cc(Br)[n+]1[O-]
Reaction #66136
2-bromo-6-methyl-4-nitro-pyridine 1-oxide
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)[n+]([O-])c(Br)c1
Reaction #66137
2-bromo-4-methoxy-6-methyl-pyridine 1-oxide
Rendement 84.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cc(Br)ncc2[N+](=O)[O-])cc1
Reaction #68930
title compound
Rendement 77.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cc(Nc3cnc(C#N)cn3)ncc2[N+](=O)[O-])cc1
Reaction #68931
title compound
Rendement 73.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cc(Br)ncc2N)cc1
Reaction #68946
title compound
Rendement 88.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cnc3cnc(Br)cc32)cc1
Reaction #68947
title compound
Rendement 108.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(N)cc1N
Reaction #79057
3-cyano-4,6-diaminopyridine
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])Nc1cc(Br)nc(Br)c1
Reaction #174548
DOI: 10.1039/C8SC04228D
O=C(Nc1ccnc(Nc2cnn(C3CCOCC3)c2)c1)c1c(Cl)cccc1Cl
Reaction #178148
DOI: 10.1039/C8SC04228D
Nc1ccc(S(=O)(=O)Nc2cc(Br)nc(Br)c2)cc1
Reaction #179473
DOI: 10.1039/C8SC04228D
O=C(Nc1ccnc(Br)c1)c1c(Cl)cccc1Cl
Reaction #183326
DOI: 10.1039/C8SC04228D
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc(-n2cccc2)ccn1
Reaction #183943
DOI: 10.1039/C8SC04228D
COc1nc(N)cc(N)c1C#N
Reaction #184882
DOI: 10.1039/C8SC04228D
CNc1cc(Br)nc(S(=O)(=O)c2ccc(N)cc2)c1
Reaction #188639
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccc(C(F)(F)F)nc1)c1cc(Br)nc(N)c1[N+](=O)[O-]
Reaction #191631
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccccc1)c1cc(NC)nc(N)c1[N+](=O)[O-]
Reaction #191889
DOI: 10.1039/C8SC04228D
NC(=S)Nc1cc(Br)nc(Br)c1
Reaction #194130
DOI: 10.1039/C8SC04228D
Nc1cnc(Br)cc1Nc1ccccc1
Reaction #208200
DOI: 10.1039/C8SC04228D
CCOC(=O)N(Cc1ccccc1)c1cc(OC)nc(N)c1[N+](=O)[O-]
Reaction #223252
DOI: 10.1039/C8SC04228D
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