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Chemical Structure| 438564-36-4 Chemical Structure| 438564-36-4

Structure of 438564-36-4

Chemical Structure| 438564-36-4

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Product Details of [ 438564-36-4 ]

CAS No. :438564-36-4
Formula : C6H4F3N3O2
M.W : 207.11
SMILES Code : NC1=CC(C(F)(F)F)=NC=C1[N+]([O-])=O
MDL No. :MFCD11848354
InChI Key :PVCDQWOCSKSIQG-UHFFFAOYSA-N
Pubchem ID :22380026

Safety of [ 438564-36-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 438564-36-4 ]

* 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 [ 438564-36-4 ]

[ 438564-36-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 438554-45-1 ]
  • [ 438564-36-4 ]
YieldReaction ConditionsOperation in experiment
100% With ammonia; In ethanol; at 20℃; for 1.5h; A pressure vessel was charged with compound 6.1 (512 mg, 0.51 mmol) and a saturated solution of ammonia in ethanol (15 mL). The vessel was sealed and the reaction mixture was stirred at room temperature for 1.5 hours, whereupon the reaction mixture was concentrated. Compound 6.3 (538 mg, >100%) was isolated as an orange solid, contaminated with inorganic salts.
96% In tetrahydrofuran; 1. Preparation of 5-Nitro-2-trifluoromethyl-pyridin-4-ylamine Ammonia gas is bubbled through a solution of 2-trifluoromethyl-4-chloro-5-nitro-pyridine (4.12 g,18.23 mmol) in anhydrous THF at room temperature for 3 h. Removal of solvent under reduced pressure affords 5-nitro-2-trifluoromethyl-pyridin-4-ylamine (3.6 g, 96%); 1H NMR (300 MHz, CDCl3): delta 7.15 (s, 1H), 9.15 (s,1H).
  • 2
  • [ 438554-45-1 ]
  • ; 194 [ No CAS ]
  • [ 438564-36-4 ]
YieldReaction ConditionsOperation in experiment
With ammonia; In ethanol; at -78 - 20℃; for 2.25h;Sealed tube; To a stirred solution of <strong>[438554-45-1]4-chloro-5-nitro-2-(trifluoromethyl)pyridine</strong> (ig, 4.42mmol) in ethanol (7mL) in sealed tube, NH3 gas was purged at -78 00 for 15 mm. The reaction mixture was stirred at room temperature for 2h. The TLC showed reaction to be complete. The reaction mixture was evaporated under reduced pressure to afford 5-nitro-2-(trifluoromethyl)pyridin-4-amine as yellow solid. Yield: ig (crude); 1H NMR (400 MHz; DMSO-d6): 9.02 (5, 1H), 7.39 (5, 1H); MS (ESl+) for CHNOS m/z 208.20 [M+H].
 

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