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N#Cc1cnccn1

CC(C)(C)NC(=O)c1cnccn1
Reaction #3742
N-tert-butyl-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)c1cnc(N)c(C#N)n1
Reaction #4539
2-amino-3-cyano-5-dimethoxymethylpyrazine
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #44288
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nccnc1Cl
Reaction #44982
title compound
Ausbeute 47.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cc(Nc3cnc(C#N)cn3)ncc2[N+](=O)[O-])cc1
Reaction #68931
title compound
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cc(Nc3cnc(C#N)cn3)ncc2N)cc1
Reaction #68932
crude title compound
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc(Nc2cc3cccc(Cl)c3cn2)nc1O[C@@H]1CCNC1
Reaction #68944
(R)-5-(8-chloroisoquinolin-3-ylamino)-3-(pyrrolidin-3-yloxy)pyrazine-2-carbonitrile
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cnc3cnc(Nc4cnc(C#N)cn4)cc32)cc1
Reaction #68948
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3[nH]cnc3cn2)cn1
Reaction #68949
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cnc(Nc2cc3[nH]cnc3cn2)cn1
Reaction #68950
title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3cc(Cl)ccc3cn2)cn1
Reaction #68954
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3cccc(-c4cc[nH]n4)c3cn2)cn1
Reaction #68956
required product
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3cccc(NCCN4CCOCC4)c3cn2)cn1
Reaction #68957
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2cc(Nc3cnc(C#N)cn3)ncc12
Reaction #68958
title compound
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3cccc(C(=O)NCCN4CCOCC4)c3cn2)cn1
Reaction #68963
title compound
Ausbeute 32.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1nc(Nc2cc3ccccc3cn2)cnc1C#N
Reaction #68968
ethyl 2-(3-cyano-6-(isoquinolin-3-ylamino)pyrazin-2-yloxy)acetate
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](C[N+](C)(C)[O-])Oc1nc(Nc2cc3cccc(Cl)c3cn2)cnc1C#N
Reaction #68970
title compound
Ausbeute 73.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3cc[nH]c3cn2)cn1
Reaction #68971
title compound
Ausbeute 45.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1cnc(C(=N)N)cn1)n2C)c1ccccn1.Cl
Reaction #78681
1-Methyl-2-[N-(2-amidinopyrazin-5-yl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide hydrochloride
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1nc(Nc2cc3ccccc3cn2)cnc1C#N
Reaction #180834
DOI: 10.1039/C8SC04228D
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