Реакция #2146795

Уравнение реакции

4-(3-iodo-6-methoxy-7-nitrobenzofuran-2-yl)-1-methyl-1H-pyrazole

3,4,5-trimethoxy thiophenol

K2CO3

2-phenylphenol

→

title compound

Выход 25.1%

6-Methoxy-2-(1-methyl-1H-pyrazol-4-yl)-7-nitro-3-(3,4,5-trimethoxyphenylthio)benzo[b]furan

Выход 25.1%

Растворители

toluene

Условия реакции

Обработка

1. 1
   Другоеwas degassed under reduced pressure and saturated with dry N2
2. 2
   Температураcooled to room temperature
3. 3
   Фильтрацияfiltered through a pad of celite
4. 4
   ПромывкаThe celite was washed with CH2Cl2 (3×20 ml)
5. 5
   ДругоеThe combined filtrates were evaporated to dryness under reduced pressure
6. 6
   Другоеthe residue was purified by flash column chromatography (silica-gel, CH2Cl2/ethyl acetate 9:1)

Методика

A modified procedure of Buchwald et al (Organic Letters 2002, 4 (20) 3517-3520) was used. A mixture of 4-(3-iodo-6-methoxy-7-nitrobenzofuran-2-yl)-1-methyl-1H-pyrazole (0.0538 g, 0.135 mmol), 3,4,5-trimethoxy thiophenol (Dawson et al, J.Am.Chem.Soc., 2002, 124, 4642-4646), (0.041 g, 0.202 mmol), dry K2CO3 (0.038 g, 0.272 mmol), CuI (0.0051 g, 0.027 mmol) and 2-phenylphenol (0.0091 g, 0.053 mmol) in dry toluene (1.5 ml) was degassed under reduced pressure and saturated with dry N2. The resulting mixture was stirred for 30 h at 110° C. under N2, cooled to room temperature and filtered through a pad of celite. The celite was washed with CH2Cl2 (3×20 ml). The combined filtrates were evaporated to dryness under reduced pressure and the residue was purified by flash column chromatography (silica-gel, CH2Cl2/ethyl acetate 9:1) giving the title compound as a creamy solid (0.016 g, 25%). 1H NMR (300 MHz, CDCl3) 8.17 (s, 1H), 8.06 (s, 1H), 7.46 (d, J=8.75 Hz, 1H), 6.94 (d, J=8.75 Hz, 1H), 6.4 (s, 2H), 3.97 (s, 3H), 3.95(s, 3H), 3.77 (s, 3H), 3.68 (s, 6H).

Источник