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Chemical Structure| 848398-40-3 Chemical Structure| 848398-40-3

Structure of 848398-40-3

Chemical Structure| 848398-40-3

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Product Details of [ 848398-40-3 ]

CAS No. :848398-40-3
Formula : C6H6N2O3
M.W : 154.12
SMILES Code : O=C1NC(COC2)=C2C(N1)=O
MDL No. :MFCD20728659

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Application In Synthesis of [ 848398-40-3 ]

* 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 [ 848398-40-3 ]

[ 848398-40-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 57595-23-0 ]
  • [ 57-13-6 ]
  • [ 848398-40-3 ]
YieldReaction ConditionsOperation in experiment
Example 1 5,7-dihydrofuro[3,4-d]pyrimidine-2,4(1H,3H)-dione: To Methyl 4-oxotetrahydrofuran-3-carboxylate (18.30 g), urea (11.44 g), methanol (100 mL) and concentrated hydrochloric acid (5 mL) were added. The mixture was refluxed with heating for two hours. The obtained suspension was stirred for 15 minutes in an ice-bath. The precipitate was filtered under reduced pressure, and washed with water (20 mL x 2 times). 2 mol/L aqueous solution of sodium hydroxide (100 mL) and water (30 mL) were added to the obtained precipitate. The mixture was refluxed with heating for 1 hour. Concentrated hydrochloric acid was dropped to the reaction solution in an ice-bath. The precipitate was filtered under reduced pressure, and then the precipitate was washed with water and acetone, dried under reduced pressure to give the title compound (15.7 g) having the following physical data. TLC: Rf 0.32 (methanol: ethyl acetate = 10 : 1); 1H-NMR (300MHz, DMSO-d6). delta 11.23, 11.44-11.10, 11.00, 4.70.
  • 2
  • [ 848398-40-3 ]
  • [ 848398-41-4 ]
YieldReaction ConditionsOperation in experiment
49% With N,N-dimethyl-aniline; trichlorophosphate; at 0℃; for 12h;Reflux; To a 0C solution of the aforementioned 3 (500 mg, 3.25 mmol) in phosphorus oxychloride (30 mL) was added dimethyl aniline (500 mg, 4.13 mmol). The resulting solution was refluxed for 12 hours. The solvents were removed under reduced pressure. The resulting residue was poured into ice (lOOg) and extracted with dichloromethane (50 mL x 3). The combined organic layers were washed with brine, dried over sodium sulfate. The Na2S04 was removed by filtration, and the volatiles were removed under reduced pressure. The resulting residue was purified by flash chromatography using a mixture of hexane and ethyl acetate to to provide the final product 4 (300 mg, 49%). LRMS (M + H+) m/z: calcd 192.01; found 192.10.
Example 2 2,4-dichloro-5,7-dihydrofuro[3,4-d]pyrimidine: Under argon gas atmosphere, phenylphosphonic dichloride (16.1 mL) was added to the compound prepared in Example 1 (15.7 g). The mixture was stirred for 6 hours at 135 C, and then for 30 minutes at 165C. After the reaction mixture was cooled, it was dropped into ice-water (100 mL). Ethyl acetate (100 mL) was added to the mixture solution. An insoluble matter was removed by filtration under reduced pressure, and was washed with ethyl acetate. The filtrate and the washings were combined, and then the mixture was shaken and separated. The organic layer was washed with a saturated sodium bicarbonate and a saturated sodium chloride, successively, dried over anhydrous sodium sulfate, and concentrated under reduced pressure, and then dried under vacuum to give the title compound (3.66 g) having the following physical data. TLC: Rf 0.60 (hexane : ethyl acetate =1:1); 1H-NMR (300MHz, CDCl3): delta 5.17, 5.09.
  • 3
  • [ 57595-23-0 ]
  • [ 848398-40-3 ]
 

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