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40149

C1=CNC2NCNC2=N1
Reaction #51649
tetrahydro-imidazopyrazine
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #53414
83
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=N[C@H](C2CCCCC(=O)C2)C(OCC)=N[C@H]1C(C)C
Reaction #164511
title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #168495
83
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(N)=NC=CN1OC
Reaction #168799
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CC(C)=C(N=[N+]=[N-])C2=C1N1CN(OC)C=C1C=N2
Reaction #186524
DOI: 10.1039/C8SC04228D
CCCNc1nc(C#N)c(C#N)nc1SCc1ccccc1
Reaction #215584
2,3-dicyano-5-n-propylamino-6-(benzylthio)pyrazine
Выход 30.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(NC3(C=N2)OCCO3)c2ccccc21
Reaction #216626
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1OC2(C=NC3=C(N2)c2ccccc2C3=O)OC1C
Reaction #216627
title compound
Выход 78.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(NC3(C=N2)SCCS3)c2ccccc21
Reaction #216635
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #305103
83
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
C1=CNC2NCNC2=N1
Reaction #317563
tetrahydro-imidazo-pyrazine
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC=CN2C1=C(c1ccc3ccc(-c4ccccc4)nc3c1)NC2C1CCC1
Reaction #331257
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1nc(C)c(C2(NS(=O)(=O)c3ccccc3)C=NC=CN2)s1
Reaction #339917
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(NC3(C=N2)OCCO3)c2ccccc21
Reaction #351081
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1OC2(C=NC3=C(N2)c2ccccc2C3=O)OC1C
Reaction #351082
title compound
Выход 78.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(NC3(C=N2)SCCS3)c2ccccc21
Reaction #351092
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)c1cc2cnc(Br)cn2n1
Reaction #428416
title compound
Выход 7.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1=NC=CN(CC)C1N
Reaction #436360
1-ethyl(propyl]pyrazine-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2C=CN=CC2)c(F)cc2c(=O)c(C(=O)O)cn(C3CC3)c12
Reaction #449773
objective compound
Выход 81.7%DOI: 10.6084/m9.figshare.5104873.v1
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