Réaction #2467964

ord-6840d895f9b141e48b3313a57056022e

Équation de réaction

O=C([O-])[O-].[K+].[K+]
K2CO3
CNC
dimethylamine
COC(=O)c1sccc1N
methyl 3-aminothiophene-2-carboxylate
Cl
HCl
O=N[O-].[Na+]
NaNO2
COC(=O)c1sccc1N=NN(C)C
solid
Rendement 91.0%
COC(=O)c1sccc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
Rendement 91.0%

Solvants

Conditions de réaction

Température
2.5°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGThe mixture was stirred at 0-10° C. for 1 h
  2. 2
    workup.ADDITIONpoured into ice cold water
  3. 3
    ExtractionThe solution was extracted with chloroform (3×100 mL)
  4. 4
    LavageThe combined layer was washed with water, brine
  5. 5
    Séchagedried over sodium sulfate
  6. 6
    FiltrationThe solution was filtered
  7. 7
    Autreevaporated the solvent
  8. 8
    AutreThe residue was chromatographed over silica gel column

Mode opératoire

To a solution of methyl 3-aminothiophene-2-carboxylate (2.0 g, 12.7 mmol) and conc. HCl (5 mL, 50.8 mmol) in H2O (30 mL) was added NaNO2 (0.96 g, 14.08 mmol) in portions for 5 min at 0° C. After stirring 0.5 h (0-5° C.), the reaction mixture was added to the solution of K2CO3 (6.65 g, 48.26 mmol) and dimethylamine (5.14 mL, 40%, 45.7 mmol) in H2O (36 mL) at 0° C. The mixture was stirred at 0-10° C. for 1 h and poured into ice cold water. The solution was extracted with chloroform (3×100 mL). The combined 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-EtOAc (80:20) as eluents to give the product as a pale orange color solid (2.5 mg, 91%), mp 74-76° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08258119B2uspto-grants-2012_09