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1336451

O=C(Cl)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #60927
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2Cl)CC1
Reaction #60936
[4-(2-Chloro-phenyl)-piperazin-1-yl]-(2-morpholin-4-yl-5-nitro-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(Cl)c1
Reaction #60941
3-Chloro-4-[4-(2-morpholin-4-yl-5-nitro-benzoyl)-piperazin-1-yl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(F)c1
Reaction #60973
Title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(C(F)(F)F)cc2Cl)CC1
Reaction #60982
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(OC(F)(F)F)cc2)CC1
Reaction #60984
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C(F)(F)F)ccc1N1CCN(C(=O)c2cc([N+](=O)[O-])ccc2N2CCOCC2)CC1
Reaction #60985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #60987
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(Cl)cc2)CC1
Reaction #60995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2F)CC1
Reaction #61007
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2Cl)CC1
Reaction #61009
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #61018
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(F)c1
Reaction #242082
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #251334
DOI: 10.1039/C8SC04228D
CCCCOC(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #264524
DOI: 10.1039/C8SC04228D
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2F)CC1
Reaction #400690
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(Cl)c1
Reaction #401290
DOI: 10.1039/C8SC04228D
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(OC(F)(F)F)cc2)CC1
Reaction #782242
DOI: 10.1039/C8SC04228D
O=C(Cl)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #823298
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2Cl)CC1
Reaction #823307
[4-(2-Chloro-phenyl)-piperazin-1-yl]-(2-morpholin-4-yl-5-nitro-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
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