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766798

Cl.Cl.NC1CCN(C2CCOCC2)CC1
Reaction #534973
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c([N+](=O)[O-])c(NC2CCN(C3CCOCC3)CC2)c1
Reaction #534974
title compound
Ausbeute 42.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC1CCN(C2CCOCC2)CC1
Reaction #660239
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine dihydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #660240
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC1CCN(C2CCOCC2)CC1
Reaction #711527
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine dihydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC1CCN(C2CCOCC2)CC1
Reaction #1130258
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine dihydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #1130259
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Cl)cc1NC1CCN(C2CCOCC2)CC1
Reaction #1289165
DOI: 10.1039/C8SC04228D
Nc1cc(Cl)c(Cl)cc1NC1CCN(C2CCOCC2)CC1
Reaction #1319911
DOI: 10.1039/C8SC04228D
Cl.Cl.NC1CCN(C2CCOCC2)CC1
Reaction #1936005
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine dihydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #1936006
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC1CCN(C2CCOCC2)CC1
Reaction #2148685
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c([N+](=O)[O-])c(NC2CCN(C3CCOCC3)CC2)c1
Reaction #2148686
title compound
Ausbeute 42.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(C2CC2)cc1NC1CCN(C2CCOCC2)CC1
Reaction #2151255
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OCC(F)(F)F)cc1NC1CCN(C2CCOCC2)CC1
Reaction #2151266
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc([N+](=O)[O-])c(NC2CCN(C3CCOCC3)CC2)c1
Reaction #2151268
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c2ccc(Cl)cc2n1C1CCN(C2CCOCC2)CC1
Reaction #2151270
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Cl)cc1NC1CCN(C2CCOCC2)CC1
Reaction #2151326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)c(Cl)cc1NC1CCN(C2CCOCC2)CC1
Reaction #2151327
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(C(F)(F)F)c(Br)cc1NC1CCN(C2CCOCC2)CC1
Reaction #2151340
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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