Substructure Search

Cc1ncn(-c2ccc(N)cc2)n1

Cc1ncn(-c2ccc(Nc3ccc4c(n3)O[C@H](c3ccccc3)CN(C)C4)cc2)n1
Reaction #308
Yield 0.0%
Cc1ncn(-c2ccc(Nc3ccc4c(n3)O[C@H](c3ccccc3)CN(C)C4)cc2)n1
Reaction #309
Yield 0.0%
Cc1ncn(-c2ccc(Nc3ccc4c(n3)O[C@H](c3ccccc3)CN(C)C4)cc2)n1
Reaction #310
Yield 0.0%
Cc1ncn(-c2ccc(Nc3ccc4c(n3)O[C@H](c3ccccc3)CN(C)C4)cc2)n1
Reaction #311
Yield 0.0%
Cc1ncn(-c2ccc(Nc3ccc4c(n3)O[C@H](c3ccccc3)CN(C)C4)cc2)n1
Reaction #312
Yield 0.0%
COc1cc(Nc2ccc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)n1
Reaction #325
Yield 19.0%
COc1cc(Nc2ccc3c(n2)O[C@H](c2ccccc2)CN(CCO)C3)ccc1-n1cnc(C)n1
Reaction #352
Yield 21.3%
CCCCc1nn(-c2ccc([N+](=O)[O-])cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1
Reaction #64524
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2ccc([N+](=O)[O-])cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(N)(=O)=O)cc1
Reaction #64525
title compound
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64526
desired material
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2ccc(NCc3ccccc3)cc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #64527
desired product
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncn(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #69006
3-methyl-1-(4-nitrophenyl)-1H-1,2,4-triazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(Nc2ccc(-n3cnc(C)n3)cc2)n1
Reaction #69007
4-methoxy-N-(4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)pyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ncn(-c2ccc(Nc3nccc(-c4cccc(N5CCOCC5)c4)n3)cc2)n1
Reaction #69019
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1N
Reaction #87560
desired product
Yield 76.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1I
Reaction #87561
desired product
Yield 54.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)ccc1[N+](=O)[O-]
Reaction #87572
desired product
Yield 65.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CN)ccc3Cl)[nH]c2=O)ccc1[N+](=O)[O-]
Reaction #87573
desired product
Yield 100.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CNC(=O)C4CC4)ccc3Cl)[nH]c2=O)ccc1[N+](=O)[O-]
Reaction #87574
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CNC(=O)C4CC4)ccc3Cl)[nH]c2=O)ccc1N
Reaction #87575
desired product
Yield 75.5%DOI: 10.6084/m9.figshare.5104873.v1
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