Reacción #1884952

Ecuación de reacción

2-(4′-Amino-3′-iodophenyl)-6-methoxy benzothiazole

BBr3

→

2-(3′-iodo-4′-aminophenyl)-6-hydroxybenzothiazole

Rendimiento 61.1%

Disolventes

CH2Cl2

CH2Cl2

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroAfter the reaction was quenched with water
2. 2
   ExtracciónThe aqueous layer was extracted with ethyl acetate (3×3 mL)
3. 3
   Secadodried over MgSO4
4. 4
   OtroThe solvent was then evaporated under reduced pressure
5. 5
   Otrothe residue was purified by preparative TLC (Hexanes:ethyl acetate=7:3)

Procedimiento

To a solution of 2-(4′-Amino-3′-iodophenyl)-6-methoxy benzothiazole (5) (8.0 mg, 0.02 mmol) in CH2Cl2 (2.0 mL) was injected 1 M BBr3 solution in CH2Cl2 (0.20 ml, 0.20 mmol) under N2 atmosphere. The reaction mixture was stirred at room temperature for 18 hrs. After the reaction was quenched with water, the mixture was neutralized with NaHCO3. The aqueous layer was extracted with ethyl acetate (3×3 mL). The organic layers were combined and dried over MgSO4. The solvent was then evaporated under reduced pressure and the residue was purified by preparative TLC (Hexanes:ethyl acetate=7:3) to give 2-(3′-iodo-4′-aminophenyl)-6-hydroxybenzothiazole (4.5 mg, 58%) as a brown solid. 1HNMR (300 MHz, acetone-d6) δ (ppm): 8.69 (s, 1H), 8.34 (d, J=2.0 Hz, 1H), 7.77 (dd, J1=2.0 Hz, J2=8.4 Hz, 1H), 7.76 (d, J=8.8 Hz, 1H), 7.40 (d, J=2.4 Hz, 1H), 7.02 (dd, J1=2.5 Hz, J2=8.8 Hz, 1H), 6.94 (d, J=8.5 Hz, 1H), 5.47 (br., 2H). HRMS m/z 367.9483 calcd for C13H9N2OSI 367.9480).

Fuente