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CAS No. : | 110871-86-8 | MDL No. : | MFCD00869619 |
Formula : | C19H22F2N4O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | DZZWHBIBMUVIIW-DTORHVGOSA-N |
M.W : | 392.40 | Pubchem ID : | 60464 |
Synonyms : |
CI-978;AT-4140;Zagam;Esparfloxacino;PD 131501;PD 1315-1;CP 103,826
|
Chemical Name : | 5-Amino-1-cyclopropyl-7-((3S,5R)-3,5-dimethylpiperazin-1-yl)-6,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
61.6% | With sodium methylate; In methanol; for 3h;pH Ca. 6.8;Reflux; | General procedure: Methanolic solution of CuCl2 2H2O (1.5 mmol) was added to a methanolic solution of 3-(diphenylphosphino)-propionic acid (L) (1.5 mmol) followed by the addition of a previously prepared methanolic solution of sparfloxacin (SFLH) (1.5 mmol) in presence of CH3ONa (1.5 mmol). The pH of the reaction mixture was adjusted to ~6.8. The resulting solution was refluxed for 3 h on a water bath, followed by concentrating to half of its volume. A fine, green amorphous product obtained was washed with ether/hexane/chloroform and dried in vacuum desiccators. The proposed reaction for the synthesis of complexes is shown in scheme 1 . Yield: 61.6%, mp: 255 C, μeff: 1.87 BM, mol. wt. 730.20, Anal. Calc. for C34H37 F2CuN4O6P, Calc. (Found) (%): C, 55.93 (55.30); H, 5.11 (5.02); N, 7.67 (7.32); Cu, 8.70 (8.40). UV-Vis: λ (nm) (ε, M-1 cm-1): 562 (160), 380 (8850), 227 (12,560), Conductance: 20 Ω-1 cm2 mol-1. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
61.48% | In methanol; for 10h;pH Ca. 6.8;Reflux; | General procedure: To a hot solution of VOSO4 (2) (5 mmol) in MeOH(25.0 mL), previously prepared methanolic solution ofligand 3-(diphenylphosphino)-propionic acid (1) (5 mmol)was added, with constant stirring. Then, alkaline methanolicsolution of ciprofloxacin (5 mmol) was added. The pH of thereaction mixture was adjusted to*6.8. The resulting greensolution was refluxed for 10 h and concentrated under vacuum.Upon addition of Et2O, a green solid precipitate wasobtained, which was collected by filtration, washed withEt2O and dried in vacuo (Gajera et al., 2015). General synthesisof complexes is shown in Scheme 1. Yield: 62.61 %.M.P:[300. Anal. Calcd (%). for C32H33FN3O6PV: C, 58.54;H, 5.07; N, 6.40; V, 7.76. Found (%): C, 58.24; H, 4.76; N,6.89; V, 7.26. UV-VIS in DMSO [kmax/nm (e/M-1 cm-1)]:421 (23,729), 584 (17,100), 807 (12,391). FT-IR: tmax(cm-1) m(C=O)pyridone 1628, m(CO2)asym 1586, m(CO2)-sym 1384, m = m(CO2)asym-m(CO2)sym = 202, m(V=O)952, m(M-O) 513 cm-1. ESI-MS (m/z):654.62 [M?]. |