An 29 Reaktionen beteiligt

C1CN(CCC1N)C2CCOCC2

N#Cc1ccc([N+](=O)[O-])c(NC2CCN(C3CCOCC3)CC2)c1
Reaction #191676
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cc(F)c(Br)cc1NC1CCN(C2CCOCC2)CC1
Reaction #221548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1cc(C(F)F)c(Cl)cc1NC1CCN(C2CCOCC2)CC1
Reaction #247268
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC1CCN(C2CCOCC2)CC1
Reaction #381983
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc(F)c([N+](=O)[O-])c(NC2CCN(C3CCOCC3)CC2)c1
Reaction #400033
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ccc(Br)cc1NC1CCN(C2CCOCC2)CC1
Reaction #404926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
NC1CCN(C2CCOCC2)CC1
Reaction #716775
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #716776
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=[N+]([O-])c1ccc(C2CC2)cc1NC1CCN(C2CCOCC2)CC1
Reaction #886065
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1ccc(OCC(F)(F)F)cc1NC1CCN(C2CCOCC2)CC1
Reaction #1038714
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
NC1CCN(C2CCOCC2)CC1
Reaction #1132345
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #1132346
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
O=[N+]([O-])c1cc(C(F)(F)F)c(Br)cc1NC1CCN(C2CCOCC2)CC1
Reaction #1208178
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=[N+]([O-])c1cc(Cl)c(Cl)cc1NC1CCN(C2CCOCC2)CC1
Reaction #1289165
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
NC1CCN(C2CCOCC2)CC1
Reaction #1605994
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #1605995
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
NC1CCN(C2CCOCC2)CC1
Reaction #1607786
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #1607787
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
NC1CCN(C2CCOCC2)CC1
Reaction #2132193
1-(tetrahydro-2H-pyran-4-yl)piperidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
NS(=O)(=O)c1ccc(NC2CCN(C3CCOCC3)CC2)c([N+](=O)[O-])c1
Reaction #2132194
3-nitro-4-(1-(tetrahydro-2H-pyran-4-yl)piperidin-4-ylamino)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
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