Reacción #2467975

ord-9dc93b4be8a24e1787872300c037ccad

Ecuación de reacción

COC(=O)c1sc([N+](=O)[O-])cc1N=NN(C)C
methyl 3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylate
[Na+].[OH-]
sodium hydroxide
CN(C)N=Nc1cc([N+](=O)[O-])sc1C(=O)O
solid
Rendimiento 86.5%
CN(C)N=Nc1cc([N+](=O)[O-])sc1C(=O)O
3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylic acid
Rendimiento 86.5%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroExcess of methanol was evaporated under reduced pressure
  2. 2
    workup.ADDITIONthe residue was diluted with ice cold water
  3. 3
    Otrothe solid separated
  4. 4
    Filtraciónwas filtered
  5. 5
    Lavadowashed with water
  6. 6
    Otrodried

Procedimiento

To a solution of methyl 3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylate (550 mg) in methanol (10 mL) was added an aqueous solution of sodium hydroxide (0.25 g in 5 mL of water) at rt and stirred the mixture for 14 h. Excess of methanol was evaporated under reduced pressure and the residue was diluted with ice cold water. The solution was acidified with dil. HCl and the solid separated was filtered, washed with water and dried to give the product as a yellow color solid (450 mg, 86%). The crude product was recrystallized from chloroform-methanol (290 mg), mp 184-186° C. 1H NMR (400 MHz, DMSO-d6): δ 13.26 (1H, br s), 8.00 (1H, s), 3.59 (3H, s), 3.25 (3H, s); LC-MS (positive ion mode): m/z 245 (M+H)+.

Fuente

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