تفاعل #1884957

ord-64be9c6243234337a7e70793f4f6778c

معادلة التفاعل

Cc1cc(OS(=O)(=O)O)c2nc(-c3ccc([N+](=O)[O-])cc3)sc2c1
2-(4′-nitrophenyl)-6-methylsulfoxy benzothiazole
O.O.[Cl][Sn][Cl]
SnCl2.2H2O
Cc1cc(OS(=O)(=O)O)c2nc(-c3ccc(N)cc3)sc2c1
2-(4′-aminophenyl)-6-methylsulfoxy benzothiazole
المردود 65.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was heated
  2. 2
    درجة الحرارةto reflux for 1.5 hr
  3. 3
    أخرىThe solvent was then removed under reduced pressure
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in ethyl acetate (10 mL)
  5. 5
    غسيلwashed with 1N NaOH, water
  6. 6
    تجفيفdried over MgSO4
  7. 7
    أخرىEvaporation of the solvent

الإجراء التجريبي

To a solution of 2-(4′-nitrophenyl)-6-methylsulfoxy benzothiazole (35 mg, 0.10 mmol) dissolved in ethanol (10 mL) was added SnCl2.2H2O (50 mg). The reaction mixture was heated to reflux for 1.5 hr. The solvent was then removed under reduced pressure. The residue was dissolved in ethyl acetate (10 mL), washed with 1N NaOH, water, dried over MgSO4. Evaporation of the solvent afforded 2-(4′-aminophenyl)-6-methylsulfoxy benzothiazole (21 mg, 65%) as pale brown solid. 1HNMR (300 MHz, CDCl3) δ (ppm): 8.02(d, J=6.2 Hz, 1H), 7.92(d, J=8.7 Hz, 2H), 7.84(d, J=2.4 Hz, 1H), 7.38(dd, J1=2.4 Hz, J2=6.2 Hz, 1H), 6.78(d, J=8.7 Hz, 2H), 2.21(s, 3H, CH3).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08343457B2uspto-grants-2013_01