بحث البنية الفرعية

1419119

O=[N+]([O-])c1ccc(N2CCOCC2)cc1
Reaction #46802
4-(4-Nitro-phenyl)-morpholine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COCCN1c1ccc([N+](=O)[O-])cc1
Reaction #46803
4-(4-Nitro-phenyl)-morpholin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(N2CCOCC2=O)cc1
Reaction #46804
4-(4-Amino-phenyl)-morpholin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)c(F)c1
Reaction #60925
title compound
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #60926
title compound
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc([N+](=O)[O-])ccc1N1CCOCC1
Reaction #60927
title compound
المردود 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
المردود 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
CC(=O)c1ccc(N2CCN(C(=O)c3cc([N+](=O)[O-])ccc3N3CCOCC3)CC2)cc1
Reaction #60990
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2F)CC1
Reaction #60992
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2)CC1
Reaction #60994
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
الصفحة 1التالي