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Cl.N=C(N)N

Cc1cc(C2C=CCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N
Reaction #2988
N-diaminomethylene-2-methyl-4-(1-cyclopentene-3-yl)-5-methylsulfonylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(C(=O)N=C(N)N)ccc1C1C=CCC1
Reaction #2990
N-diaminomethylene-3-methylsulfonyl-4-(1-cyclopenten-3-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(C)c(C(=O)N=C(N)N)cc1S(C)(=O)=O
Reaction #2991
N-diaminomethylene-2-methyl-4-ethenyl-5-methylsulfonyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(O)cc(O)n1
Reaction #3142
4,6-dihydroxy-2-methylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(O)cc(CCl)n1
Reaction #4001
2-amino-4-chloromethyl-6-hydroxypyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(O)cc(C=C(Cl)Cl)n1
Reaction #4002
2-amino-4-(2,2-dichloro-vinyl)-6-hydroxypyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc2nc(N)nc(N)c2c1
Reaction #4541
2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbonitrile
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc2nc(N)nc(N)c2c1
Reaction #4544
7
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(C)nc1-c1ccc(OC)c(OC)c1
Reaction #4775
ethyl 2-methyl-4-(3,4-dimethoxyphenyl)-5-pyrimidinecarboxylate
Ausbeute 45.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(O)cc(-c2ccc(F)cc2)n1
Reaction #8794
target compound
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1Oc1c(O)nc(C)nc1O
Reaction #10336
5-(o-methoxyphenoxy)-4,6-dihydroxy-2-methyl-pyrimidine
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C1CCc2cccc(-c3ccnc(N)n3)c2C1
Reaction #50426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Nc2nc(Cc3c(Cl)cccc3Cl)nc(NC(=N)N)n2)cc1
Reaction #53331
N-[4-[(4-cyanophenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-guanidine
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1-c1cc(=O)[nH]c(C)n1
Reaction #56833
6-(5-chloro-2-methoxy-phenyl)-2-methyl-3H-pyrimidin-4-one
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=N)N.Cl
Reaction #56837
acetamidine hydrochloride
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)nc(N)nc1O
Reaction #56843
2-amino-4,6-dihydroxy-5-methyl-pyrimidine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=N)NNC(=O)c1ccc(Cl)cc1
Reaction #58085
4-chloro-benzoic acid N′-(1-imino-ethyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc(-c2ccncc2)c(-c2ccc(OCc3ccc4ccccc4n3)cc2)n1
Reaction #62114
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2
Reaction #62740
2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2
Reaction #62745
yellow solid
Ausbeute 42.8%DOI: 10.6084/m9.figshare.5104873.v1
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