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Chemical Structure| 473839-20-2 Chemical Structure| 473839-20-2

Structure of 473839-20-2

Chemical Structure| 473839-20-2

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Product Details of [ 473839-20-2 ]

CAS No. :473839-20-2
Formula : C21H26FN3O4
M.W : 403.45
SMILES Code : O=C(O)C1=CN(C2=C(C1=O)C=C(C(N3CC(C)([C@H](CC3)N)C)=C2OC)F)C4CC4
English Name :WCK-1152

Safety of [ 473839-20-2 ]

Application In Synthesis of [ 473839-20-2 ]

* 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.

  • Downstream synthetic route of [ 473839-20-2 ]

[ 473839-20-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 115685-58-0 ]
  • [ 2270947-77-6 ]
  • [ 473839-20-2 ]
YieldReaction ConditionsOperation in experiment
Stage #1: [1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate-O3,O4]difluoroboron; (-)-4-t-butoxycarbonylamino-3,3-dimethylpiperidine In acetonitrile at 25 - 35℃; for 24h; Stage #2: With triethylamine at 80 - 85℃; Further stages; S-( )-1-Cyclopropyl-6-fluoro-8-methoxy-7-(4-amino 3, 3-dimethylpiperidin-1-yl) 1,4-dihydro-4-oxo-quinoline-3-carboxylic acid hydrochloride(Table 1, entry 4). ( )-4-t-butoxycarbonylamino-3,3-dimethylpiperidine (46 g, 0.2 m)was suspended in 200 ml acetonitrile under stirring. To the solution wasadded (1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxo-quinoline-3-carboxylate O3,O4) difluoroboron chelate (35 g, 0.10 m) and thereaction mixture was stirred for 24 h between 25 and 35 C temperature.Triethylamine (14 ml, 0.10 m) was added to the reaction mixture andstirred at 80-85 C for 4-5 h. Solvent was removed under vacuum todryness to obtain a residue, it was charged 200 ml ethanol followed bytriethylamine (17 ml, 0.12 m). The reaction mixture was refluxed for5-6 h. The resultant solution was left overnight at 25-35 C. Solidseparated was filtered and washed with additional 50 ml ethanol. Residuewas stirred with concentrated hydrochloric acid (100 ml) for 1 h atroom temperature. Resulting solution was taken to dryness by evaporatingthe acid under vacuum to obtain a residue which was treated withacetone and chloroform similar like WCK 919. Reaction mixture wasfiltered; residue was suspended in methanol 1.3 lit and dissolved atrefluxed temperature. It was filtered hot and concentrated to approximatelyone fourth of its volume and left overnight. Crystals obtainedwere filtered at 25-35 C, dried in an oven at 70-80 C. under vacuum toyield 15 g (33.5%) titled compound, m. p. 246-48 C, C21H26FN3O4.HCl,m/z 404 (M + 1), [α]D = - 1340, 1H NMR (200 MHz, Methanol-D4): 8.74(1H, s, H-2), 7.72 (1H, d, H-5, J = 16 Hz), 4.07 (1H, m, -CH), 3.64 (3H, s,-OCH3), 2.98-3.7 (5H, m, -NCH & 2 X -NCH2), 1.92 (2H, m, -CH2),0.88-1.42 (4H, m, 2 X -CH2), 0.98 (6H, s, 2 X -CH3).
Stage #1: [1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate-O3,O4]difluoroboron; (-)-4-t-butoxycarbonylamino-3,3-dimethylpiperidine In acetonitrile at 25 - 35℃; for 24h; Stage #2: With triethylamine at 80 - 85℃; Further stages; S-( )-1-Cyclopropyl-6-fluoro-8-methoxy-7-(4-amino 3, 3-dimethylpiperidin-1-yl) 1,4-dihydro-4-oxo-quinoline-3-carboxylic acid hydrochloride(Table 1, entry 4). ( )-4-t-butoxycarbonylamino-3,3-dimethylpiperidine (46 g, 0.2 m)was suspended in 200 ml acetonitrile under stirring. To the solution wasadded (1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxo-quinoline-3-carboxylate O3,O4) difluoroboron chelate (35 g, 0.10 m) and thereaction mixture was stirred for 24 h between 25 and 35 C temperature.Triethylamine (14 ml, 0.10 m) was added to the reaction mixture andstirred at 80-85 C for 4-5 h. Solvent was removed under vacuum todryness to obtain a residue, it was charged 200 ml ethanol followed bytriethylamine (17 ml, 0.12 m). The reaction mixture was refluxed for5-6 h. The resultant solution was left overnight at 25-35 C. Solidseparated was filtered and washed with additional 50 ml ethanol. Residuewas stirred with concentrated hydrochloric acid (100 ml) for 1 h atroom temperature. Resulting solution was taken to dryness by evaporatingthe acid under vacuum to obtain a residue which was treated withacetone and chloroform similar like WCK 919. Reaction mixture wasfiltered; residue was suspended in methanol 1.3 lit and dissolved atrefluxed temperature. It was filtered hot and concentrated to approximatelyone fourth of its volume and left overnight. Crystals obtainedwere filtered at 25-35 C, dried in an oven at 70-80 C. under vacuum toyield 15 g (33.5%) titled compound, m. p. 246-48 C, C21H26FN3O4.HCl,m/z 404 (M + 1), [α]D = - 1340, 1H NMR (200 MHz, Methanol-D4): 8.74(1H, s, H-2), 7.72 (1H, d, H-5, J = 16 Hz), 4.07 (1H, m, -CH), 3.64 (3H, s,-OCH3), 2.98-3.7 (5H, m, -NCH & 2 X -NCH2), 1.92 (2H, m, -CH2),0.88-1.42 (4H, m, 2 X -CH2), 0.98 (6H, s, 2 X -CH3).
 

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