Reacción #302852

ord-4cc3a8d306b54112b67df2218e15704c

Ecuación de reacción

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc2oc(-c3ccc(N(C)C)cc3)cc(=O)c2c1
compound 9
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc2oc(-c3ccc(N(C)C)cc3)cc(=O)c2c1
6-(tributylstannyl)-4′-dimethylaminoflavone
II
iodine
O=S([O-])O.[Na+]
sodium bisulfite
CN(C)c1ccc(-c2cc(=O)c3cc(I)ccc3o2)cc1
compound 11
CN(C)c1ccc(-c2cc(=O)c3cc(I)ccc3o2)cc1
6-iodo-4′-dimethylaminoflavone

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat room temperature
  2. 2
    OtroThe obtained mixture was reacted at room temperature for 30 minutes
  3. 3
    Otroso as to terminate
  4. 4
    Otrothe reaction
  5. 5
    OtroThe chloroform layer was separated
  6. 6
    Secadoit was then dried over sodium sulfate
  7. 7
    workup.DISTILLATIONThereafter, the solvent was distilled away under reduced pressure

Procedimiento

A chloroform solution of iodine (1 ml, 1 M) was added to a chloroform solution (5 ml) that contained compound 9 (30 mg, 0.054 mmol) at room temperature. The obtained mixture was reacted at room temperature for 30 minutes, and a saturated sodium bisulfite aqueous solution (5 ml) was then added thereto, so as to terminate the reaction. The chloroform layer was separated, and it was then dried over sodium sulfate. Thereafter, the solvent was distilled away under reduced pressure, and the residue was then subjected to silica gel column chromatography using ethyl acetate/hexane (1/9) as an elution solvent, so as to obtain a product of interest, 6-iodo-4′-dimethylaminoflavone (compound 11). Yield: 10 mg (yield constant: 47.3%) 1H NMR (300 MHz, CDCl3) δ8.54 (s, 1H), 7.92 (d, J=9.0 Hz, 1H), 7.81 (d, J=9.0 Hz, 2H), 7.29 (d, J=9.0 Hz, 1H), 6.71-6.80 (m, 3H), 3.09 (s, 6H). MS m/z 392 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08192717B2uspto-grants-2012_06