Teilstruktursuche

804975

COc1cc([N+](=O)[O-])ccc1OCCCN1CCN(c2cc(=O)n(C)c(=O)n2C)CC1
Reaction #201402
DOI: 10.1039/C8SC04228D
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3Cl)CC2)cc(=O)n(C)c1=O
Reaction #222744
DOI: 10.1039/C8SC04228D
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3C(=O)O)CC2)cc(=O)n(C)c1=O
Reaction #368382
DOI: 10.1039/C8SC04228D
Cl
Reaction #766178
DOI: 10.1039/C8SC04228D
Cn1c(N2CCN(CCCOc3ccc(N)cc3)CC2)cc(=O)n(C)c1=O
Reaction #1028203
DOI: 10.1039/C8SC04228D
Cl.Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3)CC2)cc(=O)n(C)c1=O
Reaction #1172435
compound 35
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cn1c(N2CCN(CCCOc3ccc(NS(C)(=O)=O)cc3[N+](=O)[O-])CC2)cc(=O)n(C)c1=O
Reaction #1172451
1,3-dimethyl-6-{4-[3-{4-methanesulfonamido-2-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione hydrochloride
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3C(=O)O)CC2)cc(=O)n(C)c1=O
Reaction #1172455
1,3-dimethyl-6-{4-[3-(2-carboxy-4-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione
Ausbeute 103.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3N)CC2)cc(=O)n(C)c1=O
Reaction #1172456
1,3-dimethyl-6-{4-[3-(2-amino-4-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione
Ausbeute 17.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3O)CC2)cc(=O)n(C)c1=O
Reaction #1172462
1,3-dimethyl-6-{4-[3-(2-hydroxy-4-nitrophenyloxy)propyl]piperazin-1-yl}-2,4(1H,3H)-pyrimidinedione
Ausbeute 78.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3NCc3ccccc3)CC2)cc(=O)n(C)c1=O
Reaction #1172463
1,3-dimethyl-6-{4-[3-(2-benzylamino-4-nitrophenyloxy)propyl]piperazin-1yl}-2,4(1H,3H)-pyrimidinedione
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc(NC(=O)C(F)(F)F)cc3)CC2)cc(=O)n(C)c1=O
Reaction #1315266
DOI: 10.1039/C8SC04228D
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3O)CC2)cc(=O)n(C)c1=O
Reaction #1661042
DOI: 10.1039/C8SC04228D
Cn1c(N2CCN(CCCOc3ccc([N+](=O)[O-])cc3Cl)CC2)cc(=O)n(C)c1=O
Reaction #1816466
light yellow crystals
Ausbeute 47.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])ccc1OCCCN1CCN(c2cc(=O)n(C)c(=O)n2C)CC1
Reaction #1816467
1,3-dimethyl-6-[4-(3-[2-methoxy-4-nitrophenyloxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione
Ausbeute 87.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc(N)cc3)CC2)cc(=O)n(C)c1=O
Reaction #1816475
6-[4-(3-[4-aminophenoxy)propyl)piperazin-1-yl]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc(NS(C)(=O)=O)cc3)CC2)cc(=O)n(C)c1=O
Reaction #1816476
1,3-dimethyl-6-[4-(3-[4-methanesulfonylaminophenoxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(N2CCN(CCCOc3ccc(NC(=O)C(F)(F)F)cc3)CC2)cc(=O)n(C)c1=O
Reaction #1816479
1,3-dimethyl-6-[4-(3-[4-trifluoroacetylaminophenoxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(N2CCN(CCCOc3ccc(NS(=O)(=O)C(F)(F)F)cc3)CC2)[nH]c(=O)[nH]1
Reaction #1816480
6-[4-(3-[4-trifluoromethanesulfonylaminophenoxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione
Ausbeute 62.5%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Nc1ccc(OCCCN2CCN(c3cc(=O)n(C)c(=O)n3C)CC2)cc1
Reaction #1816481
1,3-dimethyl-6-[4-(3-[4-(N'-methylureido)phenoxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione
Ausbeute 179.3%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter