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C1=C(C(=CN=C1N)C#N)N

CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C#N
Reaction #129
Ausbeute 50.0%
CNC(=O)c1ccccc1Nc1cc(Nc2cc(OC)nn2C)ncc1C#N
Reaction #130
Ausbeute 54.7%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #131
Ausbeute 7.3%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #132
Ausbeute 54.9%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #133
Ausbeute 43.8%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #134
Ausbeute 15.6%
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #178
Ausbeute 33.2%
N#Cc1cnc(N)cc1N
Reaction #3511
2,4-diamino-5-cyanopyridine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccnc(N)c1C=O
Reaction #3512
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2nc[nH]c(=S)c2cn1
Reaction #79035
7-amino-4-thiono-3H-pyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(N)cc1N
Reaction #79057
3-cyano-4,6-diaminopyridine
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2nc(NCc3ccccc3)ncc2cn1
Reaction #79083
7-amino-2-benzylaminopyrido[4,3-d]pyrimidine
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O.Nc1cc2ncnc(NCc3ccc(Cl)cc3)c2cn1
Reaction #79088
7-Amino-4-(4-chlorobenzylamino)pyrido[4,3-d]pyrimidine Mesylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1c(F)c(Nc2cc(C3CC3)[nH]n2)nc(N[C@@H](C)c2ccc(F)cc2)c1C#N
Reaction #163088
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1c(F)c(Nc2cc(C3CC3)[nH]n2)nc(N[C@@H](C)c2ccc(F)cc2)c1C#N
Reaction #163089
title compound
Ausbeute 51.4%DOI: 10.6084/m9.figshare.5104873.v1
[Cl-]
Reaction #177694
DOI: 10.1039/C8SC04228D
CCOc1nc(NC(C)=O)cc(N)c1C#N
Reaction #179491
DOI: 10.1039/C8SC04228D
COc1nc(N)cc(N)c1C#N
Reaction #184882
DOI: 10.1039/C8SC04228D
CCOc1nc(NC(=O)COC)cc(N)c1C#N
Reaction #223160
DOI: 10.1039/C8SC04228D
N#Cc1cnc(N)cc1N
Reaction #252283
DOI: 10.1039/C8SC04228D
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