반응 #302851

ord-7b4ea587df7d4e989b4921161f990e8e

반응 방정식

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc2oc(-c3ccc(NC)cc3)cc(=O)c2c1
compound 8
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc2oc(-c3ccc(NC)cc3)cc(=O)c2c1
6-(tributylstannyl)-4′-methylaminoflavone
II
iodine
O=S([O-])O.[Na+]
sodium bisulfite
CNc1ccc(-c2cc(=O)c3cc(I)ccc3o2)cc1
compound 10
CNc1ccc(-c2cc(=O)c3cc(I)ccc3o2)cc1
6-iodo-4′-methylaminoflavone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at room temperature
  2. 2
    기타The obtained mixture was reacted at room temperature for 10 minutes
  3. 3
    기타so as to terminate
  4. 4
    기타the reaction
  5. 5
    기타The chloroform layer was separated
  6. 6
    건조it was then dried over sodium sulfate
  7. 7
    workup.DISTILLATIONThereafter, the solvent was distilled away under reduced pressure

실험 절차

A chloroform solution of iodine (1.5 ml, 1 M) was added to a chloroform solution (20 ml) that contained compound 8 (100 mg, 0.185 mmol) at room temperature. The obtained mixture was reacted at room temperature for 10 minutes, and a saturated sodium bisulfite aqueous solution (15 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 (1/2) as an elution solvent, so as to obtain a product of interest, 6-iodo-4′-methylaminoflavone (compound 10). Yield: 20 mg (yield constant: 28.7%) 1H NMR (300 MHz, CDCl3) δ8.53 (s, 1H), 7.90 (d, J=9.0 Hz, 1H), 7.75 (d, J=8.4 Hz, 2H), 7.28 (d, J=10.8 Hz, 1H), 6.64-6.69 (m, 3H), 4.15 (s, 1H), 2.93 (s, 3H). MS m/z 377 (M+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08192717B2uspto-grants-2012_06