Substructure Search

705688

CCOC(=O)C(=CN(c1c([N+](=O)[O-])cc(F)c(N2CCN(C(=O)OCC)CC2)c1C)C1CC1)C(=O)OCC
Reaction #1021478
DOI: 10.1039/C8SC04228D
COCc1c(NC2CC2)c([N+](=O)[O-])cc(F)c1N1CCN(C)CC1
Reaction #1307698
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #1660654
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #1725850
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1c([N+](=O)[O-])cc(F)c(N2CCN(C(=O)OCC)CC2)c1C)C1CC1)C(=O)OCC
Reaction #1725851
diethyl [N-cyclopropyl-N-[3-(4-ethoxycarbonyl-1-piperazinyl)-2-methyl-4-fluoro-6-nitrophenyl]aminomethylene]malonate
Yield 51.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C2CC2)c2c(C)c(N3CCN(C(=O)OCC)CC3)c(F)cc2c1=O
Reaction #1725852
ethyl 1-cyclopropyl-7-(4-ethoxycarbonyl-1-piperazinyl)-6-fluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate
Yield 22.9%DOI: 10.6084/m9.figshare.5104873.v1
COCc1c(NC2CC2)c([N+](=O)[O-])cc(F)c1N1CCN(C)CC1
Reaction #1725854
N-Cyclopropyl-2-methoxymethyl-3-(4-methyl-1-piperazinyl)-4-fluoro-6-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #1809468
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1c([N+](=O)[O-])cc(F)c(N2CCN(C(=O)OCC)CC2)c1C)C1CC1)C(=O)OCC
Reaction #1809469
diethyl [N-cyclopropyl-N-[3-(4-ethoxycarbonyl-1-piperazinyl)-2-methyl-4-fluoro-6-nitrophenyl]aminomethylene]malonate
Yield 51.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #2194775
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1c([N+](=O)[O-])cc(F)c(N2CCN(C(=O)OCC)CC2)c1C)C1CC1)C(=O)OCC
Reaction #2194776
diethyl [N-cyclopropyl-N-[3-(4-ethoxycarbonyl-1-piperazinyl)-2-methyl-4-fluoro-6-nitrophenyl]aminomethylene]malonate
Yield 51.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C2CC2)c2c(C)c(N3CCN(C(=O)OCC)CC3)c(F)cc2c1=O
Reaction #2194777
ethyl 1-cyclopropyl-7-(4-ethoxycarbonyl-1-piperazinyl)-6-fluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate
Yield 22.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCN(c2c(F)cc([N+](=O)[O-])c(NC3CC3)c2C)CC1
Reaction #2439085
N-cyclopropyl-2-methyl-3-(4-ethoxycarbonyl-1-piperazinyl)-4-fluoro-6-nitroaniline
Yield 93.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1c([N+](=O)[O-])cc(F)c(N2CCN(C(=O)OCC)CC2)c1C)C1CC1)C(=O)OCC
Reaction #2439086
diethyl [N-cyclopropyl-N-[3-(4-ethoxycarbonyl-1-piperazinyl)-2-methyl-4-fluoro-6-nitrophenyl]aminomethylene]malonate
Yield 51.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C2CC2)c2c(C)c(N3CCN(C(=O)OCC)CC3)c(F)cc2c1=O
Reaction #2439087
ethyl 1-cyclopropyl-7-(4-ethoxycarbonyl-1-piperazinyl)-6-fluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate
Yield 22.9%DOI: 10.6084/m9.figshare.5104873.v1