Реакция #2146780

Уравнение реакции

2-iodo-5-methoxy-phenol

4-ethynyl-1-(4-methoxy-benzyl)-1H-pyrazole

3,4,5-trimethoxy-iodo-benzene

potassium carbonate

→

title compound

6-Methoxy-2-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan

Растворители

methanol

ethyl acetate

—

hexanes

Условия реакции

Обработка

1. 1
   Другоеto afford

Методика

This compound was prepared by application of the general procedure to 2-iodo-5-methoxy-phenol, 4-ethynyl-1-(4-methoxy-benzyl)-1H-pyrazole and 3,4,5-trimethoxy-iodo-benzene. The crude product was stirred with potassium carbonate (excess) in methanol for 3 h to hydrolyse ester by-products and submitted to silica-gel flash chromatography (eluent=2:1 hexanes: ethyl acetate) to afford a mixture of the title compound and the corresponding non-carbonyl inserted derivative. This mixture was used directly in the subsequent deprotection. An analytical sample was purified by recrystallisation from dichloromethane/hexane. 1H-NMR (CDCl3) δ 8.03 (s, 1H), 8.01 (s, 1H), 7.18 (d, J=8.6 Hz, 2H), 7.14 (d, J=8.7 Hz, 1H), 7.10 (s, 2H), 7.02 (d, J=2.2 Hz, 1H), 6.86 (d, J=8.6 Hz, 2H), 6.79 (dd, J=8.7, 2.2 Hz, 1H), 5.22 (s, 2H), 3.92 (s, 3H), 3.85 (s, 3H), 3.78 (s, 3H), 3.75 (s, 6H). 13C—NMR (CDCl3) δ 190.2, 159.5, 158.1, 154.2, 153.3, 152.9, 142.3, 139.1, 133.6, 129.8, 129.3, 127.6, 121.7, 120.9, 114.2, 113.8, 112.9, 112.2, 107.0, 95.5, 60.9, 56.1, 55.8, 55.6, 55.2.

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