Reacción #2467991

ord-5ea5e641734e4af6957e5afe93148d4b

Ecuación de reacción

O=[N+]([O-])O
nitric acid
O=S(=O)(O)O
sulfuric acid
Cn1nnc2sccc2c1=O
3-methylthiopheno[2,3-d]1,2,3-triazin-4-one
Cn1nnc2sc([N+](=O)[O-])cc2c1=O
solid
Rendimiento 51.1%
Cn1nnc2sc([N+](=O)[O-])cc2c1=O
3-methyl-6-nitrothiopheno[2,3-d]1,2,3-triazin-4-one
Rendimiento 51.1%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas attained to rt
  2. 2
    workup.ADDITIONThe mixture was poured into ice cold water
  3. 3
    workup.STIRRINGstirred for 15 min
  4. 4
    FiltraciónThe precipitated solid was filtered
  5. 5
    Otropurified by silica gel column chromatography

Procedimiento

To an ice cold (−10° C.) solution of concentrated sulfuric acid (5 mL) was added 3-methylthiopheno[2,3-d]1,2,3-triazin-4-one (0.6 g, 3.6 mmol) for 10 min., nitric acid (0.4 mL, 9 mmol) was added to the above reaction mixture for 5 min and the mixture was attained to rt and stirred for 1 h. The mixture was poured into ice cold water and stirred for 15 min. The precipitated solid was filtered and purified by silica gel column chromatography using hexane-chloroform (1:1) as eluents to give the product as a pale yellow color solid (390 mg, 51%), mp 164-168° C. 1H NMR (400 MHz, DMSO-d6): δ 8.60 (1H, s), 3.99 (3H, s).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08258119B2uspto-grants-2012_09