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Chemical Structure| 652-62-0 Chemical Structure| 652-62-0

Structure of 652-62-0

Chemical Structure| 652-62-0

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Product Details of [ 652-62-0 ]

CAS No. :652-62-0
Formula : C5H4F3N3O4
M.W : 227.10
SMILES Code : OC1=NC(C(F)(F)F)NC(O)=C1[N+]([O-])=O
MDL No. :MFCD08436607

Safety of [ 652-62-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 652-62-0 ]

* 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.

  • Downstream synthetic route of [ 652-62-0 ]

[ 652-62-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 672-47-9 ]
  • [ 652-62-0 ]
YieldReaction ConditionsOperation in experiment
5-Nitro-2-(trifluoromethyl)pyrimidine-4,6-diol (16) Dihydroxypyrimidine 15 (1.0 g, 5.6 mmol) was dissolved in TFA (2 mL) and stirred for 15 min at RT. Fuming nitric acid (0.325 mL) was added drop-wise, maintaining the temperature <25C, and the reaction was stirred overnight. Water was added to the reaction mixture, which was then extracted with ethyl acetate (2 x 20 mL). The organic extracts were dried over MgS04, filtered and concentrated to provide 851 mg of nitropyrimidine 16 as an off-white solid. LCMS m/z 224.1 (M+1 ). 9F NMR (376 MHz, DMSO-cfe) δ -70.45 (s, 3 F).
With nitric acid; at 4 - 6℃; for 1.5h; 6-chloro-5-nitro-2-(trifluoromethyl)pyrimidin-4-ol:; 58 %5 mL (122.2 mmoles, 11 eq.) of fuming HNO3 were cooled at +4C (int. T). Then 2 g (11.11 mmoles, 1.0 eq.) 2-(trifluoromethyl)pyrimidine-4,6-diol of were added portionwise in order to maintain the temperature between +4 and +6C. After completion of the addition, the solution was stirred at +4C for 1.5h. The mixture was poured into 25 mL of iced water and the aqueous solution was stirred for 20 min. The solution was then evaporated under reduced pressure to dryness. The resulting solid was dried under vacuum overnight to give 2.72 g of a yellow solid. This compound was used in the next step without further purifications.LC-MS : Tr = 2.10 min. (95.7 %) (no ionization) [Column : Nucleosil C-18HD, 4x70 mm, 3μm, gradient CH3CN/H2O/TFA 0.05% : 0-100% CH3CN (6 min.), 100% CH3CN (1.5 min.), flow : 1 mL/min]. EPO <DP n="28"/>13C-NMR (DMSO-D6, 100 MHz) δ : 118.7 (q, J = 258.1 Hz) ; 120.6 ; 151.9 (q, J = 32.2 Hz) ; 162.6.
 

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