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N=C(N)Nc1cccc(C(F)(F)F)c1.O=[N+]([O-])O
Reaction #2251
3-trifluoromethyl-phenylguanidine nitrate
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(Nc2nccc(-c3ccnc(Cl)c3)n2)c1
Reaction #2252
N-(3-trifluoromethyl-phenyl)-4-(2-chloro-4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
NC(=[NH2+])Nc1ccccc1.O=[N+]([O-])[O-]
Reaction #8589
N-phenylguanidinium nitrate
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nn3c(NC4CCCC4)cccc3c2-c2ccnc(Nc3ccccc3)n2)cc1
Reaction #8590
3-(2-anilino-4-pyrimidinyl)-N-cyclopentyl-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridin-7-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(N)=[NH2+])cc(OC)c1OC.O=[N+]([O-])[O-]
Reaction #8591
N-(3,4,5-trimethoxyphenyl)guanidinium nitrate
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(N)=[NH2+])cc1.O=[N+]([O-])[O-]
Reaction #8592
N-(4Methoxyphenyl)guanidinium nitrate
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=[NH2+])Nc1cccc(C(=O)c2ccccc2)c1.O=[N+]([O-])[O-]
Reaction #8598
N-(3-benzoylphenyl)guanidinium nitrate
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nn3c(NC4CCCC4)cccc3c2-c2ccnc(Nc3ccccc3-c3cccc(C=O)c3)n2)cc1
Reaction #8599
3-({(4-[7-(Cyclopentylamino)-2-(4methoxyphenyl)pyrazolo[1,5-α]pyridin-3-yl]-2-pyrimidinyl}amino)phenyl](phenyl)methanone
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nn3ccc(Cl)cc3c2-c2ccnc(Nc3ccccc3)n2)cc1
Reaction #8605
4-[5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridin-3-yl]-N-phenyl-2-pyrimidinamine
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([N+](=O)[O-])cc1NC(=N)N
Reaction #42045
objective compound
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=N)NC(=O)N(C)c1c(C)cccc1C.O=[N+]([O-])O
Reaction #54296
1-(2',6'-dimethylphenyl)-1-methyl-3-methylamidinourea nitrate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #60639
3-Dimethylamino-1-(2-ethylamino-4-methyl-thiazol-5-yl)-propenone
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(Nc2cc(-c3ccc(Cl)cc3)ccn2)cc1
Reaction #61724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cccnc2)ccn1
Reaction #69107
yellow crystals
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1ccc(Cl)cc1.O=[N+]([O-])O
Reaction #75474
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1cccc([N+](=O)[O-])c1.O=[N+]([O-])O
Reaction #75476
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C)c(-c2ccnc(Nc3cccc([N+](=O)[O-])c3)n2)s1
Reaction #75477
title compound
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1ccc(F)cc1.O=[N+]([O-])O
Reaction #75478
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C)c(-c2ccnc(Nc3ccc(F)cc3)n2)s1
Reaction #75479
title compound
Ausbeute 89.6%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1ccc(F)cc1F.O=[N+]([O-])O
Reaction #75480
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
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