Реакция #595386
ord-b32cfd92338740f69c71778beb3ab80b
Уравнение реакции
(3-bromo-1H-indazol-1-yl)(2-chloro-6-(trifluoro methyl)phenyl)methanone
K2CO3
→
title compound
5-(1-(2-chloro-6-(trifluoromethyl)benzoyl)-1H-indazol-3-yl)isobenzo furan-1 (3H)-one
Реагенты
Растворители
Условия реакции
Температура
100°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ТемператураThe reaction mixture was cooled to rt
- 2ЭкстракцияThe aqueous layer was extracted with EtOAc
- 3ПромывкаThe combined organic layers were washed with brine
- 4Сушкаdried over Na2SO4
- 5Концентрированиеconcentrated
- 6ДругоеThe residue was purified by flash chromatography (PE:EA=4:1)
Методика
(0.97 g, 2.48 mmol), (3-bromo-1H-indazol-1-yl)(2-chloro-6-(trifluoro methyl)phenyl)methanone (1.0 g, 2.48 mmol), K2CO3 (1.03 g, 7.44 mmol) and Pd(PPh3)4 (0.143 g, 0.12 mmol) were suspended in 1,4-dioxane (15 mL) and H2O (3 mL). The reaction mixture was heated at 100° C. in a microwave reactor for 2 h. The reaction mixture was cooled to rt and diluted with H2O. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated. The residue was purified by flash chromatography (PE:EA=4:1) to afford the title compound as a pale yellow oil. LCMS (ESI) calc'd for C23H13ClF3N2O3 [M+H]+: 457. found: 457.