반응 #2467986

ord-2be28bae742f463ebe1f90f00839ac40

반응 방정식

Cl
HCl
O=N[O-].[Na+]
NaNO2
COC(=O)c1cscc1N
methyl 4-aminothiophene-3-carboxylate
O=C([O-])[O-].[K+].[K+]
K2CO3
CNC
dimethylamine
COC(=O)c1cscc1N=NN(C)C
oil
수율 8.0%
COC(=O)c1cscc1N=NN(C)C
Methyl 4-[(dimethylamino)diazenyl]thiophene-3-carboxylate
수율 8.0%

용매

반응 조건

온도
2.5°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe mixture was stirred at 0-5° C. for 1 h
  2. 2
    workup.ADDITIONpoured into ice cold water
  3. 3
    추출The solution was extracted with chloroform (3×30 mL)
  4. 4
    세척The combined CHCl3 layer was washed with water, brine
  5. 5
    건조dried over sodium sulfate
  6. 6
    여과The solution was filtered
  7. 7
    기타evaporated the solvent
  8. 8
    기타The residue was chromatographed over silica gel column

실험 절차

To a solution of methyl 4-aminothiophene-3-carboxylate (200 mg, 1.27 mmol) and cone. HCl (0.5 mL, 5.09 mmol) in H2O (5 mL) was added NaNO2 (96 mg, 1.39 mmol) in portions for 5 min at 0° C. After stirring for 0.5 h at 0-5° C., the reaction mixture was added to the solution of K2CO3 (665 mg, 4.8 mmol) and dimethylamine (0.5 mL, 40%, 4.57 mmol) in H2O (5 mL) at 0° C. The mixture was stirred at 0-5° C. for 1 h and poured into ice cold water. The solution was extracted with chloroform (3×30 mL). The combined CHCl3 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 (90:10) as eluents to give the product as pale red color oil (20 mg, 8%). 1H NMR (400 MHz, CDCl3): δ 8.00 (1H, d, J=2.8 Hz), 6.97 (1H, d, J=3.6 Hz), 3.85 (3H, s), 3.34 (6H, br s).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08258119B2uspto-grants-2012_09