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Chemical Structure| 150812-23-0 Chemical Structure| 150812-23-0

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Chemical Structure| 150812-23-0

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Product Details of [ 150812-23-0 ]

CAS No. :150812-23-0
Formula : C16H16FN3O4
M.W : 333.31
SMILES Code : O=C(OCC)NC1=CC=C(NCC2=CC=C(F)C=C2)C=C1[N+]([O-])=O
MDL No. :MFCD18711763

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Application In Synthesis of [ 150812-23-0 ]

* 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.

  • Upstream synthesis route of [ 150812-23-0 ]

[ 150812-23-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 150812-23-0 ]
  • [ 150812-12-7 ]
YieldReaction ConditionsOperation in experiment
90% With hydrogen In ethanol at 50 - 70℃; for 3 h; Inert atmosphere; Industry scale A pressure vessel was charged with 2-ethyoxycarbonylamino-5-(4-fluorobenzylamino)- nitrobenzene, 1 kg (1 wt), and the catalyst, 1 percent Pt + 2 percent V/C, 50 g (0.05 wt). The vessel was pressure test with nitrogen to 6 barg. The reactor was charged with denatured ethanol, 10 L (10 vol), and the stir rate was set to > 450 rpm. The vessel was pressure purged 3 times with nitrogen to 2 barg. The reaction mixture was heated to 50 °C under reactor control. Once an internal temperature of 50 °C was achieved, agitation was discontinued and the reactor purged three times with hydrogen to 2 barg. Following the third hydrogen purge and once the vessel reached 2 barg again, hydrogen flow control was initiated and the agitator activated. The reactor contents were aged for 2 hours. The reaction was heated to 70 °C and stirred for an additional 1 hour at 70° C. Once complete, the reaction mixture was filtered. The filtrate was transfer to a second 20 L vessel. The reactor was rinsed with denatured ethanol, 3 L (3 vol) and heated to > 55 °C. The rinse was filtered and the solution transferred to the second 20-L vessel. Once the batch temperature dropped below 30 °C, a vacuum was established, 100 mbar (solution will boil at ~ 29 °C), and the solution concentrated to 7.5 L (7.5 vol). The solution was heated to 65 °C and aged until dissolution has occurred. The batch was cooled to 50 °C and seeded with retigabine (API), 5 g (0.005 wt) slurried in denatured ethanol, 20 ml_ (0.02 vol). After charging the seed, the solution was immediately cooled to 40 °C over 40 minutes, then aged for 60 min. The solution was cooled to 0 °C over 2 hours. The heterogeneous solution was stirred at 0 °C for 1 hour. The batch was milled, isolated and dried. The slurry was transferred to a filter and filtered. The wet cake was transferred to the vacuum oven and dried at 30-40 °C until the LOD indicated < 0.5 percent wt. loss (120 °C for 15 minutes).Percent yield range observed: 70-90 percent
83.5% With palladium 10% on activated carbon; ammonia; hydrogen In methanol at 25 - 30℃; Inert atmosphere; Autoclave Experiment- 14: In an autoclave vessel, 2-ethoxycarbonylamino-5-(4- fluorobenzylamino) nitrobenzene (60 g) and 10percent Pd-C (1.8 g) are added into methanolic ammonia solution (1percent w/w) (1200 ml) under nitrogen atmosphere. The reaction mixture is hydrogenated at 3-4 Kg/cm pressure at 25-30°C for 2.5-3.5 hours. After completion of reaction, activated charcoal (5percent w/w) is added and reaction mixture is stirred for 30 minutes at 25-30°C before filtration through hyflo bed under inert atmosphere. Methanolic ammonia is distilled upto 3 volumes under vacuum at 40-45 °C, then reaction mass is cooled to 0-5 °C and stirred at 0-5°C for 1 hour. Solid appeared is filtered, washed with chilled methanol and dried under vacuum at 40-45°C to get Retigabine base (45.6 g) as light grey to off-white coloured crystalline material. Yield: 83.5percent; HPLC Purity: 99.95percent, any single impurity < 0.1percent.
24.6 g With hydrogenchloride; iron In ethanol; water at 25℃; for 1 h; 80 g of intermediate is dissolved in ethanol (640 mL), and the solution is acidified by adding 36percent HCl (160 mL) Iron powder is added (32.2 g), and the mixture is maintained under stirring for one hour at about 25° C. The end-of-reaction mixture is then filtered, and the solid obtained is divided between a dilute aqueous solution of K2CO3 and ethyl acetate. The phases are separated and the organic phase is concentrated at low pressure to obtain a residue which, when taken up with isopropanol (50 mL), leads to the formation of an abundant solid. The mixture is then filtered, and the product obtained is recrystallised from isopropanol (90 mL) When the crystals have been stove-dried under vacuum at 40° C., 24.6 g of product is obtained, with chemico-physical and spectroscopic characteristics identical to those reported for compound (I) in Die Pharmazie 1998, 53, 865-869.
References: [1] Patent: WO2012/98075, 2012, A1, . Location in patent: Page/Page column 8.
[2] Patent: WO2013/11518, 2013, A1, . Location in patent: Page/Page column 45-46.
[3] Patent: US2014/163252, 2014, A1, . Location in patent: Paragraph 0042.
 

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