Reaction #2467964

ord-6840d895f9b141e48b3313a57056022e

Reaction equation

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
Yield 91.0%
COC(=O)c1sccc1N=NN(C)C
Methyl 3-[(dimethylamino)diazenyl]thiophene-2-carboxylate
Yield 91.0%

Solvents

Conditions

Temperature
2.5°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  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
    WashThe combined layer was washed with water, brine
  5. 5
    Dryingdried over sodium sulfate
  6. 6
    FiltrationThe solution was filtered
  7. 7
    Otherevaporated the solvent
  8. 8
    OtherThe residue was chromatographed over silica gel column

Procedure

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.v1Patent: US08258119B2uspto-grants-2012_09