Reacción #2467974

ord-32927d07dc9a4b12b90a4504c6ae7db0

Ecuación de reacción

COC(=O)c1sccc1N=NN(C)C
methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
[Na+].[OH-]
sodium hydroxide
Cl
HCl
CN(C)N=Nc1ccsc1C(=O)O
product
Rendimiento 38.0%
CN(C)N=Nc1ccsc1C(=O)O
3-[(dimethylamino)diazenyl]thiophene-2-carboxylic acid
Rendimiento 38.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThe mixture was diluted with ice cold water
  2. 2
    Extracciónextracted with chloroform
  3. 3
    LavadoThe combined chloroform layer was washed with water, brine
  4. 4
    Secadodried over sodium sulfate
  5. 5
    FiltraciónThe solution was filtered
  6. 6
    Otroevaporated the solvent
  7. 7
    OtroThe residue was chromatographed over silica gel column

Procedimiento

To a solution of methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate (200 mg, 0.93 mmol) in methanol (10 mL) was added a solution of sodium hydroxide (93 mg, 2.3 mmol) in water (2 mL) and stirred at rt for 2 h. The mixture was diluted with ice cold water and acidified with dil. HCl and extracted with chloroform. The combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (80:20) as eluents to give the product as an off-white solid (70 mg, 38%), mp 108-110° C. IR (neat) νmax 3402, 3082, 2923, 1708, 1218, 1116, 1066, 1016, 880, 773 cm−1; 1H NMR (400 MHz, CDCl3): δ 12.21 (1H, s), 7.47 (1H, d, J=5.2 Hz), 7.30 (1H, d, J=5.2 Hz), 3.65 (3H, s), 3.28 (3H, s); LC-MS (positive ion mode): m/z 200 (M+H)+.

Fuente

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