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19504

CN1CCN(c2ccc(N)cc2F)CC1
Reaction #10871
3-fluoro-4-(4-methyl-1-piperazinyl)benzenamine
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N=C=S)cc2F)CC1
Reaction #10872
1-(2-fluoro-4-isothio-cyanatophenyl)-4-methylpiperazine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc([N+](=O)[O-])c(N)c2F)CC1
Reaction #41797
2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41802
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41803
2
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41804
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41805
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41806
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41807
2
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(N)c(N)c2F)CC1
Reaction #41809
diamine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84382
solid
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCN(C)CC3)c(F)c2)c(C)n1
Reaction #84383
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCN(c2ccc(-n3c(C)nc(C)cc3=O)cc2F)CC1
Reaction #84474
title compound
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCN(C)CC3)c(F)c2)c(COc2cccc(F)c2)n1
Reaction #84536
title compound
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc([N+](=O)[O-])cc2F)CC1
Reaction #85834
tert-butyl 4-(2-fluoro-4-nitrophenyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2F)CC1
Reaction #85835
tert-butyl 4-(4-amino-2-fluorophenyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1N1CCNCC1
Reaction #85836
1-(4-bromo-2-fluorophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2c(F)cc(N)cc2F)CC1
Reaction #164610
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2c(F)cc(NC(=O)OCc3ccccc3)cc2F)CC1
Reaction #164611
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(N)cc2F)CC1=O
Reaction #173916
DOI: 10.1039/C8SC04228D
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