Реакция #1563867

ord-6051d7c35b32423baded1805a880bdec

Уравнение реакции

O=C([O-])[O-].[K+].[K+]
K2CO3
Brc1cnn(-c2ccccc2)c1
4-Bromo-1-phenyl-1H-pyrazole
OB(O)c1cccs1
thiophen-2-ylboronic acid
c1ccc(-n2cc(-c3cccs3)cn2)cc1
1-phenyl-4-(thiophen-2-yl)-1H-pyrazole
Выход 27.6%

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe reaction mixture was then filtered
  2. 2
    Промывкаwashed with toluene-methanol (5 ml)
  3. 3
    Концентрированиеthe filtrate was concentrated
  4. 4
    Другоеcolumn purified

Методика

4-Bromo-1-phenyl-1H-pyrazole (150 mg, 0.672 mmol), thiophen-2-ylboronic acid (296 mg, 2.31 mmol), PEPPSI-iPr (13.6 mg, 0.062 mmol), and K2CO3 (480 mg, 3.48 mmol) were combined in toluene-methanol (1:1) (2 ml). The reaction mixture was heated under microwave at 80° C. for 10 minutes. The reaction mixture was then filtered and washed with toluene-methanol (5 ml), and the filtrate was concentrated. The crude mixture was then column purified using 15-20% ethyl acetate/hexane to yield 1-phenyl-4-(thiophen-2-yl)-1H-pyrazole (42 mg, yield 27%). The HPLC purity of the final product was 99.32%. LC-MS [M+H] 227 (C13H10N2S+H expected 227.06). The 1H-NMR spectra was in accordance with the chemical structure.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09402397B2uspto-grants-2016_08