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Chemical Structure| 127168-78-9 Chemical Structure| 127168-78-9

Structure of 127168-78-9

Chemical Structure| 127168-78-9

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Product Details of [ 127168-78-9 ]

CAS No. :127168-78-9
Formula : C8H8FN
M.W : 137.15
SMILES Code : FC1=CC=CC2=C1CNC2
MDL No. :MFCD09027772
InChI Key :UDBMWFNXDSVYBR-UHFFFAOYSA-N
Pubchem ID :14795867

Safety of [ 127168-78-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 127168-78-9 ]

* 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 [ 127168-78-9 ]

[ 127168-78-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 127168-78-9 ]
  • [ 93107-30-3 ]
  • 7-(4-fluoro-2-isoindolinyl)-1-cyclopropyl-6-fluoro 1,4-dihydro-4-oxoquinoline-3-carboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
With acetic acid; In ethanol; chloroform; N,N-dimethyl-formamide; Example 21 7-(4-fluoro-2-isoindolinyl)-1-cyclopropyl-6-fluoro 1,4- dihydro-4-oxoquinoline-3-carboxylic acid STR157 A mixture of 136 mg of 1-cyclopropyl-6,7-difluoro-1,4- dihydro-4-oxoquinoline-3-carboxylic acid, 206 mg of 4-fluoroisoindoline, and 1.5 ml of anhydrous DMF was heated at 110° C. for 1.5 hours while stirring. The resulting reaction mixture was evaporated under reduced pressure to dryness. 20 ml of chloroform and 10 ml of 5percent acetic acid were added to the residue thus obtained, and the mixture was stirred. The deposited crystals were collected by filtration and washed with water and then ethanol. The chloroform layer was separated, washed with water, dried over anhydrous sodium sulfate, and condensed. The residue was crystallized by the addition of hot ethanol. After cooling the mixture, the crystals were collected by filtration. These crystals, combined with the crystals obtained above, were recrystallized from a mixed solvent of chloroform, methanol, and ethanol to obtain 85 mg of the target compound. Melting Point: 294°-299° C. (decomposed) 1 H-NMR (DMSO-d6) delta:8.65 (1H s, C2 --H) 7.94 1H, d,
  • 2
  • [ 51108-29-3 ]
  • [ 127168-78-9 ]
YieldReaction ConditionsOperation in experiment
> 80% To the starting material in a round bottom flask was added 4 equivalents of 1 M BH3- THF drop wise using an addition funnel to form a golden solution which upon heating and stirring turned copper in color. The reaction was then heated at reflux for 18 h. [00590] The reaction is then cooled to room temperature (rt) and then to 0 C in an ice bath. 4 equivalents of MeOH are added drop wise and the ice bath removed so quenched reaction can warm to rt. Reaction color turns dark during this warming process. Next, 6 N HC1 was added drop wise at rt until pH paper showed reaction to be acidic and the reaction refluxed (63 C) for 1 h. The reaction was then cooled to rt. At this point the reaction was concentrated and washed with Et2O (2x) and DCM (2x). The aqueous layer was then brought to pH = 11 with NaOH pellets. More water was added and the aqueous layer was extracted with ether (4x). The combined extracts were dried over Na2S04 and concentrated to give a light tan colored oil product, which was used directly. Mass recovery is always slightly higher than theoretical, but material is used crude like this to give > 80 % yield in the next step.
To compound 13 (4.0 g, 24.2 mmol) in a round bottom flask was added 1M BH3 in THF solution (97 mL, 97 mmol) dropwise at room temperature. The resulting solution was warmed to reflux for 18 hours. Then the reaction mixture was cooled to 0 0C and methanol (3.1 g, 97 mmol) was added dropwise. The resulting mixture was warmed up to room temperature and then 6 M HCl was added dropwise to adjust the reaction pH to 3, followed by refluxed for 1 hour. <n="54"/>After the reaction was completed, the solvents were removed under reduced pressure to give an brown oil. The residue was washed with Et2O (2x50 ml) and CH2Cl2 (2x50 mL). The aqueous phase was adjusted to pH 11 with NaOH. Then the aqueous layer was extracted with ether (4x50 mL), dried over Na2SO4, and filtered. Solvents were removed under reduced pressure to give a dark red residue. The pure compound was purified by distillation (2 mmHg, 45 0C) to give compound 14 (1.2 g).
  • 3
  • [ 443-82-3 ]
  • [ 127168-78-9 ]
 

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